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pspcas9 bb 2a gfp vector  (Addgene inc)


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    Structured Review

    Addgene inc pspcas9 bb 2a gfp vector
    Pspcas9 Bb 2a Gfp Vector, supplied by Addgene inc, used in various techniques. Bioz Stars score: 96/100, based on 4125 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/pspcas9+bb+2a+gfp/pSpCas9(BB)-2A-GFP+(PX458)+(Plasmid+%2348138)/bio_rxiv__64898__2026__10__15__759098-285-7-10
    Average 96 stars, based on 4125 article reviews
    pspcas9 bb 2a gfp vector - by Bioz Stars, 2026-11
    96/100 stars

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    Related Articles

    Clone Assay:

    Article Title: The lncRNA DAMER selectively guides m 6 A-dependent regulation of ATF4 and asparagine metabolism under nutrient stress in cancer.
    Article Snippet: How cancer cells couple metabolic stress sensing to orchestrate specific survival programmes is a key question.. Here we show a long non-coding RNA (lncRNA)-guided epitranscriptomic mechanism orchestrating metabolic adaptation by controlling the stability of master stress regulator ATF4.. Glucose or glutamine deprivation induces endoplasmic reticulum stress via reactive oxygen species–NRF2-dependent transcription of the lncRNA DAMER.

    Article Title: A lipid transfer-dependent feedback loop activates ATG9A compartments in autophagy initiation.
    Article Snippet: Candidate singleguide RNAs (sgRNAs) were identified using CRISPick (RRID:SCR_025148; https://portals.broadinstitute.org/gppx/crispick/ public), targeting all common splicing variants. .. The sgRNAs were ordered as short oligonucleotides (Microsynth AG) and cloned into pSpCas9(BB)−2A-GFP (Addgene_4813888) or pSpCas9(BB)−2AmCherrry (Addgene_19742089) vector. ..

    Article Title: Alternative splicing fine-tunes modular protein interfaces to control protein localization.
    Article Snippet: .. First, we cloned gRNAs targeting SNX2, either previously described73 or predicted using the CRISPRscan online tool74, into the pSpCas9(BB)-2A-GFP (PX458)75 (Addgene, 48138) plasmid under a U6 promoter. ..

    Transfection:

    Article Title: MMRi62 induces iron depletion–driven apoptosis through a ferritin-independent mechanism
    Article Snippet: Cells were grown at 37 °C/5% CO 2 in DMEM (Gibco, Thermo Fisher Scientific Inc, MA, USA) supplemented with 8% Gibco Fetal Bovine Serum (FBS, certified, heat inactivated, Thermo Fisher Scientific Inc, MA, USA). .. DAOY and HD-MB03 wildtype (WT) cells were transfected using jetPEI (Polyplus, 101000053) according to the manufacturers instructions with pSpCas9(BB)-2A-GFP (PX458) plasmid (a gift from Feng Zhang; Addgene plasmid #48138; http://n2t.net/addgene:48138 ; research re-source identifier: Addgene_48138) ( ) containing clustered regularly interspaced short palindromic repeats (CRISPR)-CRISPR-associated protein 9 (Cas9) targeting the following regions: FTH1 exon 1 immediate flanking region gRNA (5′- G TTACCTGTCCATGgtgagcg - 3′), and FTH1 exon 3 gRNA (5′- gggttccaatactcacATGG - 3′) or NCOA4 exon 2 : 5-GTGAGGTGTAGTGATGCACGG-3 and NCOA4 exon 3 : 5- GTCTTAGAAGCCGTGAGGTA-3. ..

    Plasmid Preparation:

    Article Title: MMRi62 induces iron depletion–driven apoptosis through a ferritin-independent mechanism
    Article Snippet: Cells were grown at 37 °C/5% CO 2 in DMEM (Gibco, Thermo Fisher Scientific Inc, MA, USA) supplemented with 8% Gibco Fetal Bovine Serum (FBS, certified, heat inactivated, Thermo Fisher Scientific Inc, MA, USA). .. DAOY and HD-MB03 wildtype (WT) cells were transfected using jetPEI (Polyplus, 101000053) according to the manufacturers instructions with pSpCas9(BB)-2A-GFP (PX458) plasmid (a gift from Feng Zhang; Addgene plasmid #48138; http://n2t.net/addgene:48138 ; research re-source identifier: Addgene_48138) ( ) containing clustered regularly interspaced short palindromic repeats (CRISPR)-CRISPR-associated protein 9 (Cas9) targeting the following regions: FTH1 exon 1 immediate flanking region gRNA (5′- G TTACCTGTCCATGgtgagcg - 3′), and FTH1 exon 3 gRNA (5′- gggttccaatactcacATGG - 3′) or NCOA4 exon 2 : 5-GTGAGGTGTAGTGATGCACGG-3 and NCOA4 exon 3 : 5- GTCTTAGAAGCCGTGAGGTA-3. ..

    Article Title: A lipid transfer-dependent feedback loop activates ATG9A compartments in autophagy initiation.
    Article Snippet: Candidate singleguide RNAs (sgRNAs) were identified using CRISPick (RRID:SCR_025148; https://portals.broadinstitute.org/gppx/crispick/ public), targeting all common splicing variants. .. The sgRNAs were ordered as short oligonucleotides (Microsynth AG) and cloned into pSpCas9(BB)−2A-GFP (Addgene_4813888) or pSpCas9(BB)−2AmCherrry (Addgene_19742089) vector. ..

    Article Title: Alternative splicing fine-tunes modular protein interfaces to control protein localization.
    Article Snippet: .. First, we cloned gRNAs targeting SNX2, either previously described73 or predicted using the CRISPRscan online tool74, into the pSpCas9(BB)-2A-GFP (PX458)75 (Addgene, 48138) plasmid under a U6 promoter. ..

    Article Title: Generation of Human Cells with Monoallelic Expression of HLA‑A in HLA Class I Knockout Cells for Evaluation of Antigen Presentation.
    Article Snippet: Cells expressing monoallelic HLA class I molecules represent a convenient in vitro model for studying the immunogenicity of tumor protein neoepitopes.. Such models can be generated using endogenous HLA class I-deficient cells.. Here, we describe an effective method for eliminating HLA class I expression in HEK293T cells via simultaneous CRISPR/Cas9 editing of the HLA-A, HLA-B, and HLA-C genes using a single guide RNA.

    CRISPR:

    Article Title: MMRi62 induces iron depletion–driven apoptosis through a ferritin-independent mechanism
    Article Snippet: Cells were grown at 37 °C/5% CO 2 in DMEM (Gibco, Thermo Fisher Scientific Inc, MA, USA) supplemented with 8% Gibco Fetal Bovine Serum (FBS, certified, heat inactivated, Thermo Fisher Scientific Inc, MA, USA). .. DAOY and HD-MB03 wildtype (WT) cells were transfected using jetPEI (Polyplus, 101000053) according to the manufacturers instructions with pSpCas9(BB)-2A-GFP (PX458) plasmid (a gift from Feng Zhang; Addgene plasmid #48138; http://n2t.net/addgene:48138 ; research re-source identifier: Addgene_48138) ( ) containing clustered regularly interspaced short palindromic repeats (CRISPR)-CRISPR-associated protein 9 (Cas9) targeting the following regions: FTH1 exon 1 immediate flanking region gRNA (5′- G TTACCTGTCCATGgtgagcg - 3′), and FTH1 exon 3 gRNA (5′- gggttccaatactcacATGG - 3′) or NCOA4 exon 2 : 5-GTGAGGTGTAGTGATGCACGG-3 and NCOA4 exon 3 : 5- GTCTTAGAAGCCGTGAGGTA-3. ..

    Article Title: The pathogenic p.D1108N SORL1 variant is dominant-negative and suitable for an antisense-oligonucleotide-mediated splice-modulating therapy for Alzheimer’s disease
    Article Snippet: .. The SORL1 knock-out (KO) was introduced in i3N-iPSCs by CRISPR/Cas9 using the pSpCas9(BB)−2A-GFP (Addgene #48138) construct and previously published gRNA targeting exon 6 of the SORL1 gene46. .. The SORL1D1108N knock-in (KI) was introduced by prime editing47 using the PEMax system48 comprised of pCMVPEMax-P2A-GFP (Addgene #180020), pU6-tevopreQ1-GG-acceptor (Addgene #174038), and pEF1a-hMLH1dn (Addgene #174824).

    Knock-Out:

    Article Title: The pathogenic p.D1108N SORL1 variant is dominant-negative and suitable for an antisense-oligonucleotide-mediated splice-modulating therapy for Alzheimer’s disease
    Article Snippet: .. The SORL1 knock-out (KO) was introduced in i3N-iPSCs by CRISPR/Cas9 using the pSpCas9(BB)−2A-GFP (Addgene #48138) construct and previously published gRNA targeting exon 6 of the SORL1 gene46. .. The SORL1D1108N knock-in (KI) was introduced by prime editing47 using the PEMax system48 comprised of pCMVPEMax-P2A-GFP (Addgene #180020), pU6-tevopreQ1-GG-acceptor (Addgene #174038), and pEF1a-hMLH1dn (Addgene #174824).

    Gene Knockout:

    Article Title: The pathogenic p.D1108N SORL1 variant is dominant-negative and suitable for an antisense-oligonucleotide-mediated splice-modulating therapy for Alzheimer’s disease
    Article Snippet: .. The SORL1 knock-out (KO) was introduced in i3N-iPSCs by CRISPR/Cas9 using the pSpCas9(BB)−2A-GFP (Addgene #48138) construct and previously published gRNA targeting exon 6 of the SORL1 gene46. .. The SORL1D1108N knock-in (KI) was introduced by prime editing47 using the PEMax system48 comprised of pCMVPEMax-P2A-GFP (Addgene #180020), pU6-tevopreQ1-GG-acceptor (Addgene #174038), and pEF1a-hMLH1dn (Addgene #174824).

    Construct:

    Article Title: The pathogenic p.D1108N SORL1 variant is dominant-negative and suitable for an antisense-oligonucleotide-mediated splice-modulating therapy for Alzheimer’s disease
    Article Snippet: .. The SORL1 knock-out (KO) was introduced in i3N-iPSCs by CRISPR/Cas9 using the pSpCas9(BB)−2A-GFP (Addgene #48138) construct and previously published gRNA targeting exon 6 of the SORL1 gene46. .. The SORL1D1108N knock-in (KI) was introduced by prime editing47 using the PEMax system48 comprised of pCMVPEMax-P2A-GFP (Addgene #180020), pU6-tevopreQ1-GG-acceptor (Addgene #174038), and pEF1a-hMLH1dn (Addgene #174824).

    Generated:

    Article Title: Generation of Human Cells with Monoallelic Expression of HLA‑A in HLA Class I Knockout Cells for Evaluation of Antigen Presentation.
    Article Snippet: Cells expressing monoallelic HLA class I molecules represent a convenient in vitro model for studying the immunogenicity of tumor protein neoepitopes.. Such models can be generated using endogenous HLA class I-deficient cells.. Here, we describe an effective method for eliminating HLA class I expression in HEK293T cells via simultaneous CRISPR/Cas9 editing of the HLA-A, HLA-B, and HLA-C genes using a single guide RNA.

    Cloning:

    Article Title: Generation of Human Cells with Monoallelic Expression of HLA‑A in HLA Class I Knockout Cells for Evaluation of Antigen Presentation.
    Article Snippet: Cells expressing monoallelic HLA class I molecules represent a convenient in vitro model for studying the immunogenicity of tumor protein neoepitopes.. Such models can be generated using endogenous HLA class I-deficient cells.. Here, we describe an effective method for eliminating HLA class I expression in HEK293T cells via simultaneous CRISPR/Cas9 editing of the HLA-A, HLA-B, and HLA-C genes using a single guide RNA.

    Ligation:

    Article Title: PrimPol toggled by ATR modulates fork slowing and repriming under oncogenic KRAS-induced replication stress
    Article Snippet: .. The annealed gRNA oligowas inserted into theBbsI site of pSpCas9(BB)−2A-GFP (Addgene, Cat# 48138) using a Quick Ligation Kit (NEB, Cat# M2200L). .. pSpCas9(ΔPP)−2A-GFP (2μg) was transfected into SAECs using Nucleofector (Lonza, Cat#VPI-1005) using the program T-013.



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    Image Search Results


    Journal: Stem Cell Reports

    Article Title: Insulin receptor substrate 2 regulates placental syncytiotrophoblast differentiation at the maternal-fetal interface

    doi: 10.1016/j.stemcr.2026.103061

    Figure Lengend Snippet:

    Article Snippet: pSpCas9(BB)-2A-GFP (PX458) plasmid , ( ) , Addgene plasmid #48138.

    Techniques: Plasmid Preparation