Review



mruby2 n1 base vector  (Addgene inc)


Bioz Verified Symbol Addgene inc is a verified supplier  
  • Logo
  • About
  • News
  • Press Release
  • Team
  • Advisors
  • Partners
  • Contact
  • Bioz Stars
  • Bioz vStars
  • 93

    Structured Review

    Addgene inc mruby2 n1 base vector
    Mruby2 N1 Base Vector, supplied by Addgene inc, used in various techniques. Bioz Stars score: 93/100, based on 18 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/mruby2+n1+vector/mRuby2-N1+(Plasmid+%2354614)/pmc09192689-494-18-21
    Average 93 stars, based on 18 article reviews
    mruby2 n1 base vector - by Bioz Stars, 2026-09
    93/100 stars

    Images

    Related Articles

    Construct:

    Article Title: Systems and methods for determining a treatment course of action
    Article Snippet: .. Lentiviral construct pLenti CMV-MRLC1-mRuby2-IRES-PuroR was generated by PCR amplification of cDNA for Homo sapiens MRLC1 from eGFP-MRLC (a gift from Tom Egelhoff, Addgene #35680) and mRuby2-N1 (a gift from Michael Davidson, Addgene #54614) to create C-terminal tagged MRLC. .. Fusion construct was subcloned into the expression vector pCIG3 (pCMVIRES-GFP, a gift from Felicia Goodrum, Addgene plasmid #78264), modified to replace the GFP cassette with puromycin resistance gene. pCMV-iRFP670-EVL-IRES-BlastR was generated by PCR amplification of cDNA for Mus musculus EVL cDNA from MSCV-eGFP-EVL and piRFP670-N1 (a gift from Vladislav Verkhusha, Addgene #45457) to create N-terminal tagged EVL.

    Article Title: IL-24 intrinsically regulates Th17 cell pathogenicity in mice
    Article Snippet: The sequences corresponding to full-length or nonsecretable (truncated) versions of IL-24, i.e., IL-24 and IL-24t, were cloned into mammalian expression vector pIRES-eGFP (6029-1; Clontech). .. The fusion constructs of nonsecretable IL-24 (mRuby2-N1-IL-24t; sequence: 5′-ATG CAA GAG TTC CGA TTT GGG TCT TGC CAA GTG ACA GGG GTG GTT CTC CCA GAA CTG TGG GAG GCC TTC TGG ACT GTG AAG AAC ACT GTG CAA ACT CAG GAT GAC ATC ACA AGC ATC CGG CTG TTG AAG CCG CAG GTT CTG CGG AAT GTC TCG GGT GCT GAG AGC TGT TAC CTT GCC CAC AGC CTG CTG AAG TTC TAC TTG AAC ACT GTT TTC AAG AAC TAC CAC AGC AAA ATA GCC AAA TTC AAG GTC TTG AGG TCA TTC TCC ACT CTG GCC AAC AAC TTC ATA GTC ATC ATG TCA CAA CTA CAG CCC AGT AAG GAC AAT TCC ATG CTT CCC ATT AGT GAG AGT GCA CAC CAG CGG TTT TTG CTG TTC CGC AGA GCA TTC AAA CAG TTG GAT ACA GAA GTC GCT TTG GTG AAA GCC TTT GGG GAA GTG GAC ATT CTC CTG ACC TGG ATG CAG AAA TTC TAC CAT CTC-3′) or IFN-γ (mRuby2-N1-IFN-γt; sequence: 5′-ATG CAC GGC ACA GTC ATT GAA AGC CTA GAA AGT CTG AAT AAC TAT TTT AAC TCA AGT GGC ATA GAT GTG GAA GAA AAG AGT CTC TTC TTG GAT ATC TGG AGG AAC TGG CAA AAG GAT GGT GAC ATG AAA ATC CTG CAG AGC CAG ATT ATC TCT TTC TAC CTC AGA CTC TTT GAA GTC TTG AAA GAC AAT CAG GCC ATC AGC AAC AAC ATA AGC GTC ATT GAA TCA CAC CTG ATT ACT ACC TTC TTC AGC AAC AGC AAG GCG AAA AAG GAT GCA TTC ATG AGT ATT GCC AAG TTT GAG GTC AAC AAC CCA CAG GTC CAG CGC CAA GCA TTC AAT GAG CTC ATC CGA GTG GTC CAC CAG CTG TTG CCG GAA TCC AGC CTC AGG AAG CGG AAA AGG AGT CGC TGC-3′) were generated by subcloning into mRuby2-N1 (54614; Addgene). .. The gRNAs targeting IL-24 or GFP were cloned into a retroviral vector (pMSCV-U6-guide-IRES-Thy1.1) using Gibson’s assembly kit (E2611S; New England Biolabs).

    Generated:

    Article Title: Systems and methods for determining a treatment course of action
    Article Snippet: .. Lentiviral construct pLenti CMV-MRLC1-mRuby2-IRES-PuroR was generated by PCR amplification of cDNA for Homo sapiens MRLC1 from eGFP-MRLC (a gift from Tom Egelhoff, Addgene #35680) and mRuby2-N1 (a gift from Michael Davidson, Addgene #54614) to create C-terminal tagged MRLC. .. Fusion construct was subcloned into the expression vector pCIG3 (pCMVIRES-GFP, a gift from Felicia Goodrum, Addgene plasmid #78264), modified to replace the GFP cassette with puromycin resistance gene. pCMV-iRFP670-EVL-IRES-BlastR was generated by PCR amplification of cDNA for Mus musculus EVL cDNA from MSCV-eGFP-EVL and piRFP670-N1 (a gift from Vladislav Verkhusha, Addgene #45457) to create N-terminal tagged EVL.

    Article Title: IL-24 intrinsically regulates Th17 cell pathogenicity in mice
    Article Snippet: The sequences corresponding to full-length or nonsecretable (truncated) versions of IL-24, i.e., IL-24 and IL-24t, were cloned into mammalian expression vector pIRES-eGFP (6029-1; Clontech). .. The fusion constructs of nonsecretable IL-24 (mRuby2-N1-IL-24t; sequence: 5′-ATG CAA GAG TTC CGA TTT GGG TCT TGC CAA GTG ACA GGG GTG GTT CTC CCA GAA CTG TGG GAG GCC TTC TGG ACT GTG AAG AAC ACT GTG CAA ACT CAG GAT GAC ATC ACA AGC ATC CGG CTG TTG AAG CCG CAG GTT CTG CGG AAT GTC TCG GGT GCT GAG AGC TGT TAC CTT GCC CAC AGC CTG CTG AAG TTC TAC TTG AAC ACT GTT TTC AAG AAC TAC CAC AGC AAA ATA GCC AAA TTC AAG GTC TTG AGG TCA TTC TCC ACT CTG GCC AAC AAC TTC ATA GTC ATC ATG TCA CAA CTA CAG CCC AGT AAG GAC AAT TCC ATG CTT CCC ATT AGT GAG AGT GCA CAC CAG CGG TTT TTG CTG TTC CGC AGA GCA TTC AAA CAG TTG GAT ACA GAA GTC GCT TTG GTG AAA GCC TTT GGG GAA GTG GAC ATT CTC CTG ACC TGG ATG CAG AAA TTC TAC CAT CTC-3′) or IFN-γ (mRuby2-N1-IFN-γt; sequence: 5′-ATG CAC GGC ACA GTC ATT GAA AGC CTA GAA AGT CTG AAT AAC TAT TTT AAC TCA AGT GGC ATA GAT GTG GAA GAA AAG AGT CTC TTC TTG GAT ATC TGG AGG AAC TGG CAA AAG GAT GGT GAC ATG AAA ATC CTG CAG AGC CAG ATT ATC TCT TTC TAC CTC AGA CTC TTT GAA GTC TTG AAA GAC AAT CAG GCC ATC AGC AAC AAC ATA AGC GTC ATT GAA TCA CAC CTG ATT ACT ACC TTC TTC AGC AAC AGC AAG GCG AAA AAG GAT GCA TTC ATG AGT ATT GCC AAG TTT GAG GTC AAC AAC CCA CAG GTC CAG CGC CAA GCA TTC AAT GAG CTC ATC CGA GTG GTC CAC CAG CTG TTG CCG GAA TCC AGC CTC AGG AAG CGG AAA AGG AGT CGC TGC-3′) were generated by subcloning into mRuby2-N1 (54614; Addgene). .. The gRNAs targeting IL-24 or GFP were cloned into a retroviral vector (pMSCV-U6-guide-IRES-Thy1.1) using Gibson’s assembly kit (E2611S; New England Biolabs).

    Polymerase Chain Reaction:

    Article Title: Systems and methods for determining a treatment course of action
    Article Snippet: .. Lentiviral construct pLenti CMV-MRLC1-mRuby2-IRES-PuroR was generated by PCR amplification of cDNA for Homo sapiens MRLC1 from eGFP-MRLC (a gift from Tom Egelhoff, Addgene #35680) and mRuby2-N1 (a gift from Michael Davidson, Addgene #54614) to create C-terminal tagged MRLC. .. Fusion construct was subcloned into the expression vector pCIG3 (pCMVIRES-GFP, a gift from Felicia Goodrum, Addgene plasmid #78264), modified to replace the GFP cassette with puromycin resistance gene. pCMV-iRFP670-EVL-IRES-BlastR was generated by PCR amplification of cDNA for Mus musculus EVL cDNA from MSCV-eGFP-EVL and piRFP670-N1 (a gift from Vladislav Verkhusha, Addgene #45457) to create N-terminal tagged EVL.

    Amplification:

    Article Title: Systems and methods for determining a treatment course of action
    Article Snippet: .. Lentiviral construct pLenti CMV-MRLC1-mRuby2-IRES-PuroR was generated by PCR amplification of cDNA for Homo sapiens MRLC1 from eGFP-MRLC (a gift from Tom Egelhoff, Addgene #35680) and mRuby2-N1 (a gift from Michael Davidson, Addgene #54614) to create C-terminal tagged MRLC. .. Fusion construct was subcloned into the expression vector pCIG3 (pCMVIRES-GFP, a gift from Felicia Goodrum, Addgene plasmid #78264), modified to replace the GFP cassette with puromycin resistance gene. pCMV-iRFP670-EVL-IRES-BlastR was generated by PCR amplification of cDNA for Mus musculus EVL cDNA from MSCV-eGFP-EVL and piRFP670-N1 (a gift from Vladislav Verkhusha, Addgene #45457) to create N-terminal tagged EVL.

    Article Title: Hijacking of transcriptional condensates by endogenous retroviruses.
    Article Snippet: To knock in the degradation-sensitive FKBPF36V tag at the N-terminus of TRIM28, a repair template containing homology arms spanning upstream and downstream of the target site was cloned into a pUC19 vector (NEB) (Supplementary Fig. 2a). .. The repair template included a mRuby2 fluorescent protein sequence, P2A linker and the FKBP tag sequence (Supplementary Fig. 2a)25. mRuby2 sequence was amplified from the mRuby2-N1 plasmid (Addgene, catalog no. 54614), and the P2A-FKBP sequence was amplified from the PITCh dTAG donor vector (Addgene, catalog no. 91792). .. A guide RNA (Supplementary Table 1b) targeting the N-terminus of TRIM28 was cloned into the sgRNA-Cas9 vector pX458 (Addgene, catalog no. 48138).

    Sequencing:

    Article Title: IL-24 intrinsically regulates Th17 cell pathogenicity in mice
    Article Snippet: The sequences corresponding to full-length or nonsecretable (truncated) versions of IL-24, i.e., IL-24 and IL-24t, were cloned into mammalian expression vector pIRES-eGFP (6029-1; Clontech). .. The fusion constructs of nonsecretable IL-24 (mRuby2-N1-IL-24t; sequence: 5′-ATG CAA GAG TTC CGA TTT GGG TCT TGC CAA GTG ACA GGG GTG GTT CTC CCA GAA CTG TGG GAG GCC TTC TGG ACT GTG AAG AAC ACT GTG CAA ACT CAG GAT GAC ATC ACA AGC ATC CGG CTG TTG AAG CCG CAG GTT CTG CGG AAT GTC TCG GGT GCT GAG AGC TGT TAC CTT GCC CAC AGC CTG CTG AAG TTC TAC TTG AAC ACT GTT TTC AAG AAC TAC CAC AGC AAA ATA GCC AAA TTC AAG GTC TTG AGG TCA TTC TCC ACT CTG GCC AAC AAC TTC ATA GTC ATC ATG TCA CAA CTA CAG CCC AGT AAG GAC AAT TCC ATG CTT CCC ATT AGT GAG AGT GCA CAC CAG CGG TTT TTG CTG TTC CGC AGA GCA TTC AAA CAG TTG GAT ACA GAA GTC GCT TTG GTG AAA GCC TTT GGG GAA GTG GAC ATT CTC CTG ACC TGG ATG CAG AAA TTC TAC CAT CTC-3′) or IFN-γ (mRuby2-N1-IFN-γt; sequence: 5′-ATG CAC GGC ACA GTC ATT GAA AGC CTA GAA AGT CTG AAT AAC TAT TTT AAC TCA AGT GGC ATA GAT GTG GAA GAA AAG AGT CTC TTC TTG GAT ATC TGG AGG AAC TGG CAA AAG GAT GGT GAC ATG AAA ATC CTG CAG AGC CAG ATT ATC TCT TTC TAC CTC AGA CTC TTT GAA GTC TTG AAA GAC AAT CAG GCC ATC AGC AAC AAC ATA AGC GTC ATT GAA TCA CAC CTG ATT ACT ACC TTC TTC AGC AAC AGC AAG GCG AAA AAG GAT GCA TTC ATG AGT ATT GCC AAG TTT GAG GTC AAC AAC CCA CAG GTC CAG CGC CAA GCA TTC AAT GAG CTC ATC CGA GTG GTC CAC CAG CTG TTG CCG GAA TCC AGC CTC AGG AAG CGG AAA AGG AGT CGC TGC-3′) were generated by subcloning into mRuby2-N1 (54614; Addgene). .. The gRNAs targeting IL-24 or GFP were cloned into a retroviral vector (pMSCV-U6-guide-IRES-Thy1.1) using Gibson’s assembly kit (E2611S; New England Biolabs).

    Article Title: Hijacking of transcriptional condensates by endogenous retroviruses.
    Article Snippet: To knock in the degradation-sensitive FKBPF36V tag at the N-terminus of TRIM28, a repair template containing homology arms spanning upstream and downstream of the target site was cloned into a pUC19 vector (NEB) (Supplementary Fig. 2a). .. The repair template included a mRuby2 fluorescent protein sequence, P2A linker and the FKBP tag sequence (Supplementary Fig. 2a)25. mRuby2 sequence was amplified from the mRuby2-N1 plasmid (Addgene, catalog no. 54614), and the P2A-FKBP sequence was amplified from the PITCh dTAG donor vector (Addgene, catalog no. 91792). .. A guide RNA (Supplementary Table 1b) targeting the N-terminus of TRIM28 was cloned into the sgRNA-Cas9 vector pX458 (Addgene, catalog no. 48138).

    Countercurrent Chromatography:

    Article Title: IL-24 intrinsically regulates Th17 cell pathogenicity in mice
    Article Snippet: The sequences corresponding to full-length or nonsecretable (truncated) versions of IL-24, i.e., IL-24 and IL-24t, were cloned into mammalian expression vector pIRES-eGFP (6029-1; Clontech). .. The fusion constructs of nonsecretable IL-24 (mRuby2-N1-IL-24t; sequence: 5′-ATG CAA GAG TTC CGA TTT GGG TCT TGC CAA GTG ACA GGG GTG GTT CTC CCA GAA CTG TGG GAG GCC TTC TGG ACT GTG AAG AAC ACT GTG CAA ACT CAG GAT GAC ATC ACA AGC ATC CGG CTG TTG AAG CCG CAG GTT CTG CGG AAT GTC TCG GGT GCT GAG AGC TGT TAC CTT GCC CAC AGC CTG CTG AAG TTC TAC TTG AAC ACT GTT TTC AAG AAC TAC CAC AGC AAA ATA GCC AAA TTC AAG GTC TTG AGG TCA TTC TCC ACT CTG GCC AAC AAC TTC ATA GTC ATC ATG TCA CAA CTA CAG CCC AGT AAG GAC AAT TCC ATG CTT CCC ATT AGT GAG AGT GCA CAC CAG CGG TTT TTG CTG TTC CGC AGA GCA TTC AAA CAG TTG GAT ACA GAA GTC GCT TTG GTG AAA GCC TTT GGG GAA GTG GAC ATT CTC CTG ACC TGG ATG CAG AAA TTC TAC CAT CTC-3′) or IFN-γ (mRuby2-N1-IFN-γt; sequence: 5′-ATG CAC GGC ACA GTC ATT GAA AGC CTA GAA AGT CTG AAT AAC TAT TTT AAC TCA AGT GGC ATA GAT GTG GAA GAA AAG AGT CTC TTC TTG GAT ATC TGG AGG AAC TGG CAA AAG GAT GGT GAC ATG AAA ATC CTG CAG AGC CAG ATT ATC TCT TTC TAC CTC AGA CTC TTT GAA GTC TTG AAA GAC AAT CAG GCC ATC AGC AAC AAC ATA AGC GTC ATT GAA TCA CAC CTG ATT ACT ACC TTC TTC AGC AAC AGC AAG GCG AAA AAG GAT GCA TTC ATG AGT ATT GCC AAG TTT GAG GTC AAC AAC CCA CAG GTC CAG CGC CAA GCA TTC AAT GAG CTC ATC CGA GTG GTC CAC CAG CTG TTG CCG GAA TCC AGC CTC AGG AAG CGG AAA AGG AGT CGC TGC-3′) were generated by subcloning into mRuby2-N1 (54614; Addgene). .. The gRNAs targeting IL-24 or GFP were cloned into a retroviral vector (pMSCV-U6-guide-IRES-Thy1.1) using Gibson’s assembly kit (E2611S; New England Biolabs).

    Subcloning:

    Article Title: IL-24 intrinsically regulates Th17 cell pathogenicity in mice
    Article Snippet: The sequences corresponding to full-length or nonsecretable (truncated) versions of IL-24, i.e., IL-24 and IL-24t, were cloned into mammalian expression vector pIRES-eGFP (6029-1; Clontech). .. The fusion constructs of nonsecretable IL-24 (mRuby2-N1-IL-24t; sequence: 5′-ATG CAA GAG TTC CGA TTT GGG TCT TGC CAA GTG ACA GGG GTG GTT CTC CCA GAA CTG TGG GAG GCC TTC TGG ACT GTG AAG AAC ACT GTG CAA ACT CAG GAT GAC ATC ACA AGC ATC CGG CTG TTG AAG CCG CAG GTT CTG CGG AAT GTC TCG GGT GCT GAG AGC TGT TAC CTT GCC CAC AGC CTG CTG AAG TTC TAC TTG AAC ACT GTT TTC AAG AAC TAC CAC AGC AAA ATA GCC AAA TTC AAG GTC TTG AGG TCA TTC TCC ACT CTG GCC AAC AAC TTC ATA GTC ATC ATG TCA CAA CTA CAG CCC AGT AAG GAC AAT TCC ATG CTT CCC ATT AGT GAG AGT GCA CAC CAG CGG TTT TTG CTG TTC CGC AGA GCA TTC AAA CAG TTG GAT ACA GAA GTC GCT TTG GTG AAA GCC TTT GGG GAA GTG GAC ATT CTC CTG ACC TGG ATG CAG AAA TTC TAC CAT CTC-3′) or IFN-γ (mRuby2-N1-IFN-γt; sequence: 5′-ATG CAC GGC ACA GTC ATT GAA AGC CTA GAA AGT CTG AAT AAC TAT TTT AAC TCA AGT GGC ATA GAT GTG GAA GAA AAG AGT CTC TTC TTG GAT ATC TGG AGG AAC TGG CAA AAG GAT GGT GAC ATG AAA ATC CTG CAG AGC CAG ATT ATC TCT TTC TAC CTC AGA CTC TTT GAA GTC TTG AAA GAC AAT CAG GCC ATC AGC AAC AAC ATA AGC GTC ATT GAA TCA CAC CTG ATT ACT ACC TTC TTC AGC AAC AGC AAG GCG AAA AAG GAT GCA TTC ATG AGT ATT GCC AAG TTT GAG GTC AAC AAC CCA CAG GTC CAG CGC CAA GCA TTC AAT GAG CTC ATC CGA GTG GTC CAC CAG CTG TTG CCG GAA TCC AGC CTC AGG AAG CGG AAA AGG AGT CGC TGC-3′) were generated by subcloning into mRuby2-N1 (54614; Addgene). .. The gRNAs targeting IL-24 or GFP were cloned into a retroviral vector (pMSCV-U6-guide-IRES-Thy1.1) using Gibson’s assembly kit (E2611S; New England Biolabs).

    Transfection:

    Article Title: Bioinformatics Analysis and Experimental Identification of Immune-Related Genes and Immune Cells in the Progression of Retinoblastoma.
    Article Snippet: In vitro and in vivo grade siRNA against SH3GL2 (si-SH3GL2) and nonspecific control siRNA (si-NC) were obtained from RiboBio (Guangzhou, China) and performed according to the manufacturer’s protocol. .. The Y79 cells were transfected with plasmid mRuby2-N1 (empty vector, OE-NC, cat. no. 54614; Addgene, Watertown, MA, USA) or plasmid EndophilinA1-mRuby2 (overexpression SH3GL2, OESH3GL2, cat. no. 171945; Addgene) by Lipofectamine 3000 transfection reagent (Invitrogen) according to the manufacturer’s protocol. ..

    Article Title: Bioinformatics Analysis and Experimental Identification of Immune-Related Genes and Immune Cells in the Progression of Retinoblastoma
    Article Snippet: In vitro and in vivo grade siRNA against SH3GL2 (si-SH3GL2) and nonspecific control siRNA (si-NC) were obtained from RiboBio (Guangzhou, China) and performed according to the manufacturer's protocol. .. The Y79 cells were transfected with plasmid mRuby2-N1 (empty vector, OE-NC, cat. no. 54614; Addgene, Watertown, MA, USA) or plasmid EndophilinA1-mRuby2 (overexpression SH3GL2, OE-SH3GL2, cat. no. 171945; Addgene) by Lipofectamine 3000 transfection reagent (Invitrogen) according to the manufacturer's protocol. ..

    Plasmid Preparation:

    Article Title: Bioinformatics Analysis and Experimental Identification of Immune-Related Genes and Immune Cells in the Progression of Retinoblastoma.
    Article Snippet: In vitro and in vivo grade siRNA against SH3GL2 (si-SH3GL2) and nonspecific control siRNA (si-NC) were obtained from RiboBio (Guangzhou, China) and performed according to the manufacturer’s protocol. .. The Y79 cells were transfected with plasmid mRuby2-N1 (empty vector, OE-NC, cat. no. 54614; Addgene, Watertown, MA, USA) or plasmid EndophilinA1-mRuby2 (overexpression SH3GL2, OESH3GL2, cat. no. 171945; Addgene) by Lipofectamine 3000 transfection reagent (Invitrogen) according to the manufacturer’s protocol. ..

    Article Title: Bioinformatics Analysis and Experimental Identification of Immune-Related Genes and Immune Cells in the Progression of Retinoblastoma
    Article Snippet: In vitro and in vivo grade siRNA against SH3GL2 (si-SH3GL2) and nonspecific control siRNA (si-NC) were obtained from RiboBio (Guangzhou, China) and performed according to the manufacturer's protocol. .. The Y79 cells were transfected with plasmid mRuby2-N1 (empty vector, OE-NC, cat. no. 54614; Addgene, Watertown, MA, USA) or plasmid EndophilinA1-mRuby2 (overexpression SH3GL2, OE-SH3GL2, cat. no. 171945; Addgene) by Lipofectamine 3000 transfection reagent (Invitrogen) according to the manufacturer's protocol. ..

    Article Title: Hijacking of transcriptional condensates by endogenous retroviruses.
    Article Snippet: To knock in the degradation-sensitive FKBPF36V tag at the N-terminus of TRIM28, a repair template containing homology arms spanning upstream and downstream of the target site was cloned into a pUC19 vector (NEB) (Supplementary Fig. 2a). .. The repair template included a mRuby2 fluorescent protein sequence, P2A linker and the FKBP tag sequence (Supplementary Fig. 2a)25. mRuby2 sequence was amplified from the mRuby2-N1 plasmid (Addgene, catalog no. 54614), and the P2A-FKBP sequence was amplified from the PITCh dTAG donor vector (Addgene, catalog no. 91792). .. A guide RNA (Supplementary Table 1b) targeting the N-terminus of TRIM28 was cloned into the sgRNA-Cas9 vector pX458 (Addgene, catalog no. 48138).

    Over Expression:

    Article Title: Bioinformatics Analysis and Experimental Identification of Immune-Related Genes and Immune Cells in the Progression of Retinoblastoma.
    Article Snippet: In vitro and in vivo grade siRNA against SH3GL2 (si-SH3GL2) and nonspecific control siRNA (si-NC) were obtained from RiboBio (Guangzhou, China) and performed according to the manufacturer’s protocol. .. The Y79 cells were transfected with plasmid mRuby2-N1 (empty vector, OE-NC, cat. no. 54614; Addgene, Watertown, MA, USA) or plasmid EndophilinA1-mRuby2 (overexpression SH3GL2, OESH3GL2, cat. no. 171945; Addgene) by Lipofectamine 3000 transfection reagent (Invitrogen) according to the manufacturer’s protocol. ..

    Article Title: Bioinformatics Analysis and Experimental Identification of Immune-Related Genes and Immune Cells in the Progression of Retinoblastoma
    Article Snippet: In vitro and in vivo grade siRNA against SH3GL2 (si-SH3GL2) and nonspecific control siRNA (si-NC) were obtained from RiboBio (Guangzhou, China) and performed according to the manufacturer's protocol. .. The Y79 cells were transfected with plasmid mRuby2-N1 (empty vector, OE-NC, cat. no. 54614; Addgene, Watertown, MA, USA) or plasmid EndophilinA1-mRuby2 (overexpression SH3GL2, OE-SH3GL2, cat. no. 171945; Addgene) by Lipofectamine 3000 transfection reagent (Invitrogen) according to the manufacturer's protocol. ..

    other:

    Article Title: Hijacking of transcriptional condensates by endogenous retroviruses.
    Article Snippet: A guide RNA (Supplementary Table 1b) targeting the N-terminus of TRIM28 was cloned into the sgRNA-Cas9 vector pX458 (Addgene, catalog no. 48138).



    Similar Products

    93
    Addgene inc mruby2 n1 base vector
    Mruby2 N1 Base Vector, supplied by Addgene inc, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/mruby2+n1+vector/mRuby2-N1+(Plasmid+%2354614)/pmc09192689-494-18-21
    Average 93 stars, based on 1 article reviews
    mruby2 n1 base vector - by Bioz Stars, 2026-09
    93/100 stars
      Buy from Supplier

    93
    Addgene inc mruby2 n1 vector
    Mruby2 N1 Vector, supplied by Addgene inc, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/mruby2+n1+vector/mRuby2-N1+(Plasmid+%2354614)/pm33965400-40-47-49
    Average 93 stars, based on 1 article reviews
    mruby2 n1 vector - by Bioz Stars, 2026-09
    93/100 stars
      Buy from Supplier

    93
    Addgene inc mclover2 c1 vector
    Mclover2 C1 Vector, supplied by Addgene inc, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/mruby2+n1+vector/mRuby2-N1+(Plasmid+%2354614)/pm33965400-40-35-37
    Average 93 stars, based on 1 article reviews
    mclover2 c1 vector - by Bioz Stars, 2026-09
    93/100 stars
      Buy from Supplier

    93
    Addgene inc mruby2 tubulin 6 vector
    CLASP2 and G2L1 colocalize in 3T3-L1 adipocytes. A–B, Live-cell imaging of adipocytes cultured in complete media coexpressing <t>mRuby2-Tubulin</t> (magenta) and GFP-CLASP2-HA (A, green) or mCherry-G2L1-myc (B, green). Live cells were imaged using TIRFM on a 2-s acquisition interval. Time series images to the right of the whole cell image are used to highlight +TIP dynamics within the indicated ROI. C, Immunofluorescence images of adipocytes cultured in complete media cooverexpressing GFP-CLASP2-HA (green) and mCherry-G2L1-myc (magenta). Cells were fixed and immunolabeled for tubulin (inverted white). Bottom row is magnified ROI. ROI, region of interest. Scale bar = 20 μm.
    Mruby2 Tubulin 6 Vector, supplied by Addgene inc, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/mruby2+n1+vector/piRFP670-N1+(Plasmid+%2345457)/pmc06601206-97-10-15
    Average 93 stars, based on 1 article reviews
    mruby2 tubulin 6 vector - by Bioz Stars, 2026-09
    93/100 stars
      Buy from Supplier

    Image Search Results


    CLASP2 and G2L1 colocalize in 3T3-L1 adipocytes. A–B, Live-cell imaging of adipocytes cultured in complete media coexpressing mRuby2-Tubulin (magenta) and GFP-CLASP2-HA (A, green) or mCherry-G2L1-myc (B, green). Live cells were imaged using TIRFM on a 2-s acquisition interval. Time series images to the right of the whole cell image are used to highlight +TIP dynamics within the indicated ROI. C, Immunofluorescence images of adipocytes cultured in complete media cooverexpressing GFP-CLASP2-HA (green) and mCherry-G2L1-myc (magenta). Cells were fixed and immunolabeled for tubulin (inverted white). Bottom row is magnified ROI. ROI, region of interest. Scale bar = 20 μm.

    Journal: Molecular & Cellular Proteomics : MCP

    Article Title: Insulin Induces Microtubule Stabilization and Regulates the Microtubule Plus-end Tracking Protein Network in Adipocytes *

    doi: 10.1074/mcp.RA119.001450

    Figure Lengend Snippet: CLASP2 and G2L1 colocalize in 3T3-L1 adipocytes. A–B, Live-cell imaging of adipocytes cultured in complete media coexpressing mRuby2-Tubulin (magenta) and GFP-CLASP2-HA (A, green) or mCherry-G2L1-myc (B, green). Live cells were imaged using TIRFM on a 2-s acquisition interval. Time series images to the right of the whole cell image are used to highlight +TIP dynamics within the indicated ROI. C, Immunofluorescence images of adipocytes cultured in complete media cooverexpressing GFP-CLASP2-HA (green) and mCherry-G2L1-myc (magenta). Cells were fixed and immunolabeled for tubulin (inverted white). Bottom row is magnified ROI. ROI, region of interest. Scale bar = 20 μm.

    Article Snippet: To generate pLenti-iRFP670-Tubulin, tubulin was first subcloned out of the mRuby2-Tubulin-6 vector and into piRFP670-N1 (Addgene #45457, a gift from Vladislav Verkhusha). iRFP670-Tubulin was then subcloned out of the piRFP670-Tubulin vector and into the pLenti backbone to generate pLenti-iRFP670-Tubulin.

    Techniques: Live Cell Imaging, Cell Culture, Immunofluorescence, Immunolabeling

    The effect of insulin on CLASP2 +TIP dynamics. Live-cell imaging of adipocytes serum-starved for one hour and subsequently stimulated with 100 nm insulin. Live cells were imaged using TIRFM on a two-second acquisition interval. A, Single frame of live-cell imaging of adipocytes coexpressing GFP-CLASP2 (green) and mRuby2-Tubulin (magenta) at basal state (top row) or 10 mins (bottom row) following insulin stimulation. CLASP2 is displayed in inverted white to highlight +TIP density. B, Quantification of CLASP2-containing +TIP density per unit area (μm2) in adipocytes at basal state or 10 mins following insulin stimulation. Percent increase in CLASP2-containing +TIP density is indicated to the right. Statistical comparison made by paired parametric t test, n = 5 cells. C, Temporally color-coded projection of GFP-CLASP2 localization during a 30 s live-cell imaging interval. The length and extent of color overlap of time-projected CLASP2 localization indicates reduced displacement and hence lower velocity of CLASP2-containing +TIPs during the imaging interval in adipocytes after 10 mins of insulin stimulation. D, Quantification of CLASP2-containing +TIP velocity in adipocytes at basal state or 10 mins following insulin stimulation indicates reduced velocity of CLASP2-containing +TIPS after insulin treatment. Statistical comparison made by unpaired parametric t test, n = 123–125 CLASP2-containing +TIPS from five cells. Scale bars = 5 μm. E, Image of entire cells in the basal state (left panel) or 8 mins post insulin treatment (right panel) extracted from supplemental Video 2. Time series images under the whole cell image are used to highlight insulin-stimulated +TIP dynamics within the indicated ROI. F, Time series extracted from supplemental Video 2 of the indicated ROIs at either the basal state or at 4 mins post insulin treatment to present an example of changing CLASP2 microtubule plus-end dynamics with insulin stimulation. G, Live cell CLASP2-containing +TIP dynamics of the ROI extracted from supplemental Video 2 were captured in the basal state followed by stimulation with insulin. Each insulin-stimulated CLASP2-containing +TIP trail length time point was compared against the basal CLASP2-containing +TIP trail length to test for significant differences. t test; *p ≤ 0.05, **p ≤ 0.01. Red circles represent outlier data points. ROI, region of interest. BAS, basal. INS, insulin. Scale bar = 10 μm.

    Journal: Molecular & Cellular Proteomics : MCP

    Article Title: Insulin Induces Microtubule Stabilization and Regulates the Microtubule Plus-end Tracking Protein Network in Adipocytes *

    doi: 10.1074/mcp.RA119.001450

    Figure Lengend Snippet: The effect of insulin on CLASP2 +TIP dynamics. Live-cell imaging of adipocytes serum-starved for one hour and subsequently stimulated with 100 nm insulin. Live cells were imaged using TIRFM on a two-second acquisition interval. A, Single frame of live-cell imaging of adipocytes coexpressing GFP-CLASP2 (green) and mRuby2-Tubulin (magenta) at basal state (top row) or 10 mins (bottom row) following insulin stimulation. CLASP2 is displayed in inverted white to highlight +TIP density. B, Quantification of CLASP2-containing +TIP density per unit area (μm2) in adipocytes at basal state or 10 mins following insulin stimulation. Percent increase in CLASP2-containing +TIP density is indicated to the right. Statistical comparison made by paired parametric t test, n = 5 cells. C, Temporally color-coded projection of GFP-CLASP2 localization during a 30 s live-cell imaging interval. The length and extent of color overlap of time-projected CLASP2 localization indicates reduced displacement and hence lower velocity of CLASP2-containing +TIPs during the imaging interval in adipocytes after 10 mins of insulin stimulation. D, Quantification of CLASP2-containing +TIP velocity in adipocytes at basal state or 10 mins following insulin stimulation indicates reduced velocity of CLASP2-containing +TIPS after insulin treatment. Statistical comparison made by unpaired parametric t test, n = 123–125 CLASP2-containing +TIPS from five cells. Scale bars = 5 μm. E, Image of entire cells in the basal state (left panel) or 8 mins post insulin treatment (right panel) extracted from supplemental Video 2. Time series images under the whole cell image are used to highlight insulin-stimulated +TIP dynamics within the indicated ROI. F, Time series extracted from supplemental Video 2 of the indicated ROIs at either the basal state or at 4 mins post insulin treatment to present an example of changing CLASP2 microtubule plus-end dynamics with insulin stimulation. G, Live cell CLASP2-containing +TIP dynamics of the ROI extracted from supplemental Video 2 were captured in the basal state followed by stimulation with insulin. Each insulin-stimulated CLASP2-containing +TIP trail length time point was compared against the basal CLASP2-containing +TIP trail length to test for significant differences. t test; *p ≤ 0.05, **p ≤ 0.01. Red circles represent outlier data points. ROI, region of interest. BAS, basal. INS, insulin. Scale bar = 10 μm.

    Article Snippet: To generate pLenti-iRFP670-Tubulin, tubulin was first subcloned out of the mRuby2-Tubulin-6 vector and into piRFP670-N1 (Addgene #45457, a gift from Vladislav Verkhusha). iRFP670-Tubulin was then subcloned out of the piRFP670-Tubulin vector and into the pLenti backbone to generate pLenti-iRFP670-Tubulin.

    Techniques: Live Cell Imaging, Imaging