Review



inactive nuclease codon optimized s pyogenes cas9  (Addgene inc)


Bioz Verified Symbol Addgene inc is a verified supplier  
  • Logo
  • About
  • News
  • Press Release
  • Team
  • Advisors
  • Partners
  • Contact
  • Bioz Stars
  • Bioz vStars
  • 94

    Structured Review

    Addgene inc inactive nuclease codon optimized s pyogenes cas9
    Inactive Nuclease Codon Optimized S Pyogenes Cas9, supplied by Addgene inc, used in various techniques. Bioz Stars score: 94/100, based on 44 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/codon+optimized+cas9/pPlatTET-gRNA2+(Plasmid+%2382559)/pm41286098-331-28-39
    Average 94 stars, based on 44 article reviews
    inactive nuclease codon optimized s pyogenes cas9 - by Bioz Stars, 2026-11
    94/100 stars

    Images

    Related Articles

    CRISPR:

    Article Title: HDAC1 has intrinsic protease activity and regulates transcription through clipping histone H3 N-terminal tail.
    Article Snippet: Histone deacetylase 1 (HDAC1) has been mainly characterized as a factor removing acetyl groups from histone and non-histone proteins as well as inhibiting gene transcription.. However, HDAC1 is also involved in positively regulating transcription of particular genes through as yet unknown mechanisms.. Here we report the identification of an intrinsic protease activity residing in HDAC1 and capable of cleaving histone H3 between lysine 20 and alanine 21.

    Expressing:

    Article Title: HDAC1 has intrinsic protease activity and regulates transcription through clipping histone H3 N-terminal tail.
    Article Snippet: Histone deacetylase 1 (HDAC1) has been mainly characterized as a factor removing acetyl groups from histone and non-histone proteins as well as inhibiting gene transcription.. However, HDAC1 is also involved in positively regulating transcription of particular genes through as yet unknown mechanisms.. Here we report the identification of an intrinsic protease activity residing in HDAC1 and capable of cleaving histone H3 between lysine 20 and alanine 21.

    Article Title: MSH2 is not required for either maintenance of DNA methylation or repeat contraction at the FMR1 locus in fragile X syndrome or the FXN locus in Friedreich's ataxia.
    Article Snippet: .. Transient transfection of dCas9-TET1 for FMR1 reactivation Gibson assembly [77] was used to construct the plasmid pMLM3636-Puro-dCas9-TET1 using NEBuilder®HiFi DNA Assembly Master Mix (New England Biolabs, E2621L) and fragments derived from the following plasmids: PuroR from pSpCas9(BB)-2 A-Puro (PX459) V2.0, a gift from Feng Zhang (Addgene plasmid # 62988; http://n2t.net/addgene:62988) [71], dCas9 from I n d u c i b l e Caspex expression, a gift from Steven Carr & Samuel Myers (Addgene plasmid # 97421; h t t p : / / n 2 t . n e t / a d d g e n e : 9 7 4 2 1 ) [78], and TET1CD from pPlatTET-gRNA2, a gift from Izuho Hatada (Addgene plasmid # 82559; http:// n2t.net/addgene:82559) [79] and vector backbone from pMLM3636 (a gift from Keith Joung (Addgene plasmid # 43860; http://n2t.net/addgene:43860). .. Transient transfection of dCas9-TET1 for FMR1 reactivation Gibson assembly [77] was used to construct the plasmid pMLM3636-Puro-dCas9-TET1 using NEBuilderHiFi DNA Assembly Master Mix (New England Biolabs, E2621L) and fragments derived from the following plasmids: PuroR from pSpCas9(BB)-2 A-Puro (PX459) V2.0, a gift from Feng Zhang (Addgene plasmid # 62988; http://n2t.net/addgene:62988) [71], dCas9 from I n d u c i b l e Caspex expression, a gift from Steven Carr & Samuel Myers (Addgene plasmid # 97421; h t t p : / / n 2 t . n e t / a d d g e n e : 9 7 4 2 1 ) [78], and TET1CD from pPlatTET-gRNA2, a gift from Izuho Hatada (Addgene plasmid # 82559; http:// n2t.net/addgene:82559) [79] and vector backbone from pMLM3636 (a gift from Keith Joung (Addgene plasmid # 43860; http://n2t.net/addgene:43860).

    Article Title: Epigenome editing-mediated restoration of FBN1 expression by demethylation of CpG island shore in porcine fibroblasts
    Article Snippet: Fibrillin-1, an extracellular matrix protein encoded by the FBN1 gene, is crucial for maintaining connective tissue integrity.. Mutations in FBN1 result in haploinsufficiency, leading to Marfan syndrome, in which the expression of functional FBN1 is correlated with disease onset and severity.. Recent studies suggest that FBN1 expression is modulated by DNA methylation, particularly within the CpG island shores of its promoter region.

    Generated:

    Article Title: HDAC1 has intrinsic protease activity and regulates transcription through clipping histone H3 N-terminal tail.
    Article Snippet: Histone deacetylase 1 (HDAC1) has been mainly characterized as a factor removing acetyl groups from histone and non-histone proteins as well as inhibiting gene transcription.. However, HDAC1 is also involved in positively regulating transcription of particular genes through as yet unknown mechanisms.. Here we report the identification of an intrinsic protease activity residing in HDAC1 and capable of cleaving histone H3 between lysine 20 and alanine 21.

    Article Title: Epigenome editing-mediated restoration of FBN1 expression by demethylation of CpG island shore in porcine fibroblasts
    Article Snippet: Fibrillin-1, an extracellular matrix protein encoded by the FBN1 gene, is crucial for maintaining connective tissue integrity.. Mutations in FBN1 result in haploinsufficiency, leading to Marfan syndrome, in which the expression of functional FBN1 is correlated with disease onset and severity.. Recent studies suggest that FBN1 expression is modulated by DNA methylation, particularly within the CpG island shores of its promoter region.

    Mutagenesis:

    Article Title: HDAC1 has intrinsic protease activity and regulates transcription through clipping histone H3 N-terminal tail.
    Article Snippet: Histone deacetylase 1 (HDAC1) has been mainly characterized as a factor removing acetyl groups from histone and non-histone proteins as well as inhibiting gene transcription.. However, HDAC1 is also involved in positively regulating transcription of particular genes through as yet unknown mechanisms.. Here we report the identification of an intrinsic protease activity residing in HDAC1 and capable of cleaving histone H3 between lysine 20 and alanine 21.

    Plasmid Preparation:

    Article Title: Rescue of imprinted genes by epigenome editing in human cellular models of Prader-Willi syndrome
    Article Snippet: .. The plasmid encoding dCas9-Suntag-TET1 components was obtained from Addgene (pPlatTET-gRNA2, #82559) and modified for the experiment. ..

    Article Title: MSH2 is not required for either maintenance of DNA methylation or repeat contraction at the FMR1 locus in fragile X syndrome or the FXN locus in Friedreich's ataxia.
    Article Snippet: .. Transient transfection of dCas9-TET1 for FMR1 reactivation Gibson assembly [77] was used to construct the plasmid pMLM3636-Puro-dCas9-TET1 using NEBuilder®HiFi DNA Assembly Master Mix (New England Biolabs, E2621L) and fragments derived from the following plasmids: PuroR from pSpCas9(BB)-2 A-Puro (PX459) V2.0, a gift from Feng Zhang (Addgene plasmid # 62988; http://n2t.net/addgene:62988) [71], dCas9 from I n d u c i b l e Caspex expression, a gift from Steven Carr & Samuel Myers (Addgene plasmid # 97421; h t t p : / / n 2 t . n e t / a d d g e n e : 9 7 4 2 1 ) [78], and TET1CD from pPlatTET-gRNA2, a gift from Izuho Hatada (Addgene plasmid # 82559; http:// n2t.net/addgene:82559) [79] and vector backbone from pMLM3636 (a gift from Keith Joung (Addgene plasmid # 43860; http://n2t.net/addgene:43860). .. Transient transfection of dCas9-TET1 for FMR1 reactivation Gibson assembly [77] was used to construct the plasmid pMLM3636-Puro-dCas9-TET1 using NEBuilderHiFi DNA Assembly Master Mix (New England Biolabs, E2621L) and fragments derived from the following plasmids: PuroR from pSpCas9(BB)-2 A-Puro (PX459) V2.0, a gift from Feng Zhang (Addgene plasmid # 62988; http://n2t.net/addgene:62988) [71], dCas9 from I n d u c i b l e Caspex expression, a gift from Steven Carr & Samuel Myers (Addgene plasmid # 97421; h t t p : / / n 2 t . n e t / a d d g e n e : 9 7 4 2 1 ) [78], and TET1CD from pPlatTET-gRNA2, a gift from Izuho Hatada (Addgene plasmid # 82559; http:// n2t.net/addgene:82559) [79] and vector backbone from pMLM3636 (a gift from Keith Joung (Addgene plasmid # 43860; http://n2t.net/addgene:43860).

    Article Title: Epigenome editing-mediated restoration of FBN1 expression by demethylation of CpG island shore in porcine fibroblasts
    Article Snippet: Fibrillin-1, an extracellular matrix protein encoded by the FBN1 gene, is crucial for maintaining connective tissue integrity.. Mutations in FBN1 result in haploinsufficiency, leading to Marfan syndrome, in which the expression of functional FBN1 is correlated with disease onset and severity.. Recent studies suggest that FBN1 expression is modulated by DNA methylation, particularly within the CpG island shores of its promoter region.

    Article Title: Germline epigenome editing identifies H3K9me3 as a mediator of intergenerational DNA methylation recovery in mice.
    Article Snippet: .. Vector construction for germline-specific demethylation The all-in-one epigenome editing vector, including dCas9 fused with five copies of GCN4 and an anti-GCN4 peptide antibody (scFv)-sfGFPTET1CD fusion protein (pPlatTET-gRNA2, Addgene plasmid 82559), was previously reported by this laboratory31. ..

    Article Title: Rescue of imprinted genes by epigenome editing in human cellular models of Prader-Willi syndrome.
    Article Snippet: .. These newly established iPSC lines are available from the lead contact on request. dCas9-Suntag-TET1 plasmids The plasmid encoding dCas9-Suntag-TET1 components was obtained from Addgene (pPlatTET-gRNA2, #82559) and modified for the experiment. ..

    Article Title: Germline epigenome editing identifies H3K9me3 as a mediator of intergenerational DNA methylation recovery in mice
    Article Snippet: .. The all-in-one epigenome editing vector, including dCas9 fused with five copies of GCN4 and an anti-GCN4 peptide antibody (scFv)-sfGFP-TET1CD fusion protein (pPlatTET-gRNA2, Addgene plasmid 82559), was previously reported by this laboratory . ..

    Modification:

    Article Title: Rescue of imprinted genes by epigenome editing in human cellular models of Prader-Willi syndrome
    Article Snippet: .. The plasmid encoding dCas9-Suntag-TET1 components was obtained from Addgene (pPlatTET-gRNA2, #82559) and modified for the experiment. ..

    Article Title: Rescue of imprinted genes by epigenome editing in human cellular models of Prader-Willi syndrome.
    Article Snippet: .. These newly established iPSC lines are available from the lead contact on request. dCas9-Suntag-TET1 plasmids The plasmid encoding dCas9-Suntag-TET1 components was obtained from Addgene (pPlatTET-gRNA2, #82559) and modified for the experiment. ..

    Transfection:

    Article Title: MSH2 is not required for either maintenance of DNA methylation or repeat contraction at the FMR1 locus in fragile X syndrome or the FXN locus in Friedreich's ataxia.
    Article Snippet: .. Transient transfection of dCas9-TET1 for FMR1 reactivation Gibson assembly [77] was used to construct the plasmid pMLM3636-Puro-dCas9-TET1 using NEBuilder®HiFi DNA Assembly Master Mix (New England Biolabs, E2621L) and fragments derived from the following plasmids: PuroR from pSpCas9(BB)-2 A-Puro (PX459) V2.0, a gift from Feng Zhang (Addgene plasmid # 62988; http://n2t.net/addgene:62988) [71], dCas9 from I n d u c i b l e Caspex expression, a gift from Steven Carr & Samuel Myers (Addgene plasmid # 97421; h t t p : / / n 2 t . n e t / a d d g e n e : 9 7 4 2 1 ) [78], and TET1CD from pPlatTET-gRNA2, a gift from Izuho Hatada (Addgene plasmid # 82559; http:// n2t.net/addgene:82559) [79] and vector backbone from pMLM3636 (a gift from Keith Joung (Addgene plasmid # 43860; http://n2t.net/addgene:43860). .. Transient transfection of dCas9-TET1 for FMR1 reactivation Gibson assembly [77] was used to construct the plasmid pMLM3636-Puro-dCas9-TET1 using NEBuilderHiFi DNA Assembly Master Mix (New England Biolabs, E2621L) and fragments derived from the following plasmids: PuroR from pSpCas9(BB)-2 A-Puro (PX459) V2.0, a gift from Feng Zhang (Addgene plasmid # 62988; http://n2t.net/addgene:62988) [71], dCas9 from I n d u c i b l e Caspex expression, a gift from Steven Carr & Samuel Myers (Addgene plasmid # 97421; h t t p : / / n 2 t . n e t / a d d g e n e : 9 7 4 2 1 ) [78], and TET1CD from pPlatTET-gRNA2, a gift from Izuho Hatada (Addgene plasmid # 82559; http:// n2t.net/addgene:82559) [79] and vector backbone from pMLM3636 (a gift from Keith Joung (Addgene plasmid # 43860; http://n2t.net/addgene:43860).

    Construct:

    Article Title: MSH2 is not required for either maintenance of DNA methylation or repeat contraction at the FMR1 locus in fragile X syndrome or the FXN locus in Friedreich's ataxia.
    Article Snippet: .. Transient transfection of dCas9-TET1 for FMR1 reactivation Gibson assembly [77] was used to construct the plasmid pMLM3636-Puro-dCas9-TET1 using NEBuilder®HiFi DNA Assembly Master Mix (New England Biolabs, E2621L) and fragments derived from the following plasmids: PuroR from pSpCas9(BB)-2 A-Puro (PX459) V2.0, a gift from Feng Zhang (Addgene plasmid # 62988; http://n2t.net/addgene:62988) [71], dCas9 from I n d u c i b l e Caspex expression, a gift from Steven Carr & Samuel Myers (Addgene plasmid # 97421; h t t p : / / n 2 t . n e t / a d d g e n e : 9 7 4 2 1 ) [78], and TET1CD from pPlatTET-gRNA2, a gift from Izuho Hatada (Addgene plasmid # 82559; http:// n2t.net/addgene:82559) [79] and vector backbone from pMLM3636 (a gift from Keith Joung (Addgene plasmid # 43860; http://n2t.net/addgene:43860). .. Transient transfection of dCas9-TET1 for FMR1 reactivation Gibson assembly [77] was used to construct the plasmid pMLM3636-Puro-dCas9-TET1 using NEBuilderHiFi DNA Assembly Master Mix (New England Biolabs, E2621L) and fragments derived from the following plasmids: PuroR from pSpCas9(BB)-2 A-Puro (PX459) V2.0, a gift from Feng Zhang (Addgene plasmid # 62988; http://n2t.net/addgene:62988) [71], dCas9 from I n d u c i b l e Caspex expression, a gift from Steven Carr & Samuel Myers (Addgene plasmid # 97421; h t t p : / / n 2 t . n e t / a d d g e n e : 9 7 4 2 1 ) [78], and TET1CD from pPlatTET-gRNA2, a gift from Izuho Hatada (Addgene plasmid # 82559; http:// n2t.net/addgene:82559) [79] and vector backbone from pMLM3636 (a gift from Keith Joung (Addgene plasmid # 43860; http://n2t.net/addgene:43860).

    Derivative Assay:

    Article Title: MSH2 is not required for either maintenance of DNA methylation or repeat contraction at the FMR1 locus in fragile X syndrome or the FXN locus in Friedreich's ataxia.
    Article Snippet: .. Transient transfection of dCas9-TET1 for FMR1 reactivation Gibson assembly [77] was used to construct the plasmid pMLM3636-Puro-dCas9-TET1 using NEBuilder®HiFi DNA Assembly Master Mix (New England Biolabs, E2621L) and fragments derived from the following plasmids: PuroR from pSpCas9(BB)-2 A-Puro (PX459) V2.0, a gift from Feng Zhang (Addgene plasmid # 62988; http://n2t.net/addgene:62988) [71], dCas9 from I n d u c i b l e Caspex expression, a gift from Steven Carr & Samuel Myers (Addgene plasmid # 97421; h t t p : / / n 2 t . n e t / a d d g e n e : 9 7 4 2 1 ) [78], and TET1CD from pPlatTET-gRNA2, a gift from Izuho Hatada (Addgene plasmid # 82559; http:// n2t.net/addgene:82559) [79] and vector backbone from pMLM3636 (a gift from Keith Joung (Addgene plasmid # 43860; http://n2t.net/addgene:43860). .. Transient transfection of dCas9-TET1 for FMR1 reactivation Gibson assembly [77] was used to construct the plasmid pMLM3636-Puro-dCas9-TET1 using NEBuilderHiFi DNA Assembly Master Mix (New England Biolabs, E2621L) and fragments derived from the following plasmids: PuroR from pSpCas9(BB)-2 A-Puro (PX459) V2.0, a gift from Feng Zhang (Addgene plasmid # 62988; http://n2t.net/addgene:62988) [71], dCas9 from I n d u c i b l e Caspex expression, a gift from Steven Carr & Samuel Myers (Addgene plasmid # 97421; h t t p : / / n 2 t . n e t / a d d g e n e : 9 7 4 2 1 ) [78], and TET1CD from pPlatTET-gRNA2, a gift from Izuho Hatada (Addgene plasmid # 82559; http:// n2t.net/addgene:82559) [79] and vector backbone from pMLM3636 (a gift from Keith Joung (Addgene plasmid # 43860; http://n2t.net/addgene:43860).

    Control:

    Article Title: Epigenome editing-mediated restoration of FBN1 expression by demethylation of CpG island shore in porcine fibroblasts
    Article Snippet: Fibrillin-1, an extracellular matrix protein encoded by the FBN1 gene, is crucial for maintaining connective tissue integrity.. Mutations in FBN1 result in haploinsufficiency, leading to Marfan syndrome, in which the expression of functional FBN1 is correlated with disease onset and severity.. Recent studies suggest that FBN1 expression is modulated by DNA methylation, particularly within the CpG island shores of its promoter region.

    Sequencing:

    Article Title: Epigenome editing-mediated restoration of FBN1 expression by demethylation of CpG island shore in porcine fibroblasts
    Article Snippet: Fibrillin-1, an extracellular matrix protein encoded by the FBN1 gene, is crucial for maintaining connective tissue integrity.. Mutations in FBN1 result in haploinsufficiency, leading to Marfan syndrome, in which the expression of functional FBN1 is correlated with disease onset and severity.. Recent studies suggest that FBN1 expression is modulated by DNA methylation, particularly within the CpG island shores of its promoter region.

    Amplification:

    Article Title:
    Article Snippet: Lenti dCAS-VP64 Blast (Addgene, Watertown, NY, USA, cat. #61425), lenti MS2-P65-HSF1 Hygro (Addgene, cat. #61426) and lenti sgRNA (MS2) zeo backbone (Addgene, cat. #61427) were gifts from Feng Zhang. .. Human TET1cd was amplified by PCR from pPlatTet-grna2 (Addgene, cat. #82559, a gift from Izuho Hatada) with either BamHI-XbaI or BamHI-BstBI as restriction sites and ligated into lenti dCAS-VP64 Blast and lenti MS2-P65-HSF1 Hygro. .. Human TET1cd was amplified by PCR from pPlatTet-grna2 (Addgene, cat. #82559, a gift from Izuho Hatada) with either BamHI-XbaI or BamHI-BstBI as restriction sites and ligated into lenti dCAS-VP64 Blast and lenti MS2-P65-HSF1 Hygro.

    Polymerase Chain Reaction:

    Article Title:
    Article Snippet: Lenti dCAS-VP64 Blast (Addgene, Watertown, NY, USA, cat. #61425), lenti MS2-P65-HSF1 Hygro (Addgene, cat. #61426) and lenti sgRNA (MS2) zeo backbone (Addgene, cat. #61427) were gifts from Feng Zhang. .. Human TET1cd was amplified by PCR from pPlatTet-grna2 (Addgene, cat. #82559, a gift from Izuho Hatada) with either BamHI-XbaI or BamHI-BstBI as restriction sites and ligated into lenti dCAS-VP64 Blast and lenti MS2-P65-HSF1 Hygro. .. Human TET1cd was amplified by PCR from pPlatTet-grna2 (Addgene, cat. #82559, a gift from Izuho Hatada) with either BamHI-XbaI or BamHI-BstBI as restriction sites and ligated into lenti dCAS-VP64 Blast and lenti MS2-P65-HSF1 Hygro.



    Similar Products

    96
    Addgene inc codon optimized cas9
    Codon Optimized Cas9, supplied by Addgene inc, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/codon+optimized+cas9/LentiV_Cas9_puro+(Plasmid+%23108100)/bio_rxiv__64898__2026__01__21__700714-205-16-22
    Average 96 stars, based on 1 article reviews
    codon optimized cas9 - by Bioz Stars, 2026-11
    96/100 stars
      Buy from Supplier

    86
    Twist Bioscience yeast codon optimized cas9 28
    Yeast Codon Optimized Cas9 28, supplied by Twist Bioscience, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/codon+optimized+cas9/cas9+crispr+design+sgrna/pm41543897-201-8-13
    Average 86 stars, based on 1 article reviews
    yeast codon optimized cas9 28 - by Bioz Stars, 2026-11
    86/100 stars
      Buy from Supplier

    99
    New England Biolabs zebrafish codon optimized cas9 plasmid pt3ts nls zcas9
    Zebrafish Codon Optimized Cas9 Plasmid Pt3ts Nls Zcas9, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/codon+optimized+cas9/XbaI/pmc12723011-423-5-15
    Average 99 stars, based on 1 article reviews
    zebrafish codon optimized cas9 plasmid pt3ts nls zcas9 - by Bioz Stars, 2026-11
    99/100 stars
      Buy from Supplier

    94
    Addgene inc inactive nuclease codon optimized s pyogenes cas9
    Inactive Nuclease Codon Optimized S Pyogenes Cas9, supplied by Addgene inc, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/codon+optimized+cas9/pPlatTET-gRNA2+(Plasmid+%2382559)/pm41286098-331-28-39
    Average 94 stars, based on 1 article reviews
    inactive nuclease codon optimized s pyogenes cas9 - by Bioz Stars, 2026-11
    94/100 stars
      Buy from Supplier

    93
    Addgene inc codon optimized streptococchus pyogenes cas9 sequence
    Codon Optimized Streptococchus Pyogenes Cas9 Sequence, 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/codon+optimized+cas9/pLentiCas9-GFP+(Plasmid+%2378546)/pm41205600-434-12-22
    Average 93 stars, based on 1 article reviews
    codon optimized streptococchus pyogenes cas9 sequence - by Bioz Stars, 2026-11
    93/100 stars
      Buy from Supplier

    95
    Addgene inc zebrafish codon optimized cas9
    Zebrafish Codon Optimized Cas9, supplied by Addgene inc, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/codon+optimized+cas9/pT3TS-nCas9n+(Plasmid+%2346757)/bio_rxiv__2025__10__24__684380-34-1-5
    Average 95 stars, based on 1 article reviews
    zebrafish codon optimized cas9 - by Bioz Stars, 2026-11
    95/100 stars
      Buy from Supplier

    96
    Addgene inc humanized codon optimized s pyogenes cas9
    Humanized Codon Optimized S Pyogenes Cas9, supplied by Addgene inc, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/codon+optimized+cas9/SP-Cas9+(Plasmid+%2362731)/us12415001-225-28-42
    Average 96 stars, based on 1 article reviews
    humanized codon optimized s pyogenes cas9 - by Bioz Stars, 2026-11
    96/100 stars
      Buy from Supplier

    94
    Addgene inc codon optimized streptococcus pyogenes cas9 spcas9 nuclease expression plasmid jds246
    Codon Optimized Streptococcus Pyogenes Cas9 Spcas9 Nuclease Expression Plasmid Jds246, supplied by Addgene inc, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/codon+optimized+cas9/JDS246+(Plasmid+%2343861)/us12404527-319-4-13
    Average 94 stars, based on 1 article reviews
    codon optimized streptococcus pyogenes cas9 spcas9 nuclease expression plasmid jds246 - by Bioz Stars, 2026-11
    94/100 stars
      Buy from Supplier

    96
    Addgene inc codon optimized s pyogenes cas9 protein
    (A) Schematic workflow of the pooled <t>CRISPR/Cas9</t> gene knockout screen. Cas9-expressing chromaffin cells were generated via lentiviral transduction and blasticidin selection. Cells were then transduced with a genome-wide sgRNA library, selected with puromycin, and cultured for 10 population doublings before genomic DNA extraction. sgRNA abundance was quantified at initial and final times by deep sequencing, and data were analyzed using the MAGeCK pipeline. (B) Ranked Robust Rank Aggregation (RRA) scores of the most significantly depleted genes from the screen. (C) Ranked RRA scores of the most significantly enriched genes from the screen. (D) Volcano plot of CRISPR screen results showing significantly depleted genes (blue) versus non-significant genes (gray). The x-axis represents log₂(fold change) (Log₂FC) in sgRNA abundance, and the y-axis shows –log₁₀ P values from MAGeCK analysis. (E) Volcano plot showing significantly enriched genes (red) versus non-significant genes (gray).
    Codon Optimized S Pyogenes Cas9 Protein, supplied by Addgene inc, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/codon+optimized+cas9/SP-Cas9+(Plasmid+%2362731)/bio_rxiv__2025__08__26__672429-132-17-30
    Average 96 stars, based on 1 article reviews
    codon optimized s pyogenes cas9 protein - by Bioz Stars, 2026-11
    96/100 stars
      Buy from Supplier

    Image Search Results


    (A) Schematic workflow of the pooled CRISPR/Cas9 gene knockout screen. Cas9-expressing chromaffin cells were generated via lentiviral transduction and blasticidin selection. Cells were then transduced with a genome-wide sgRNA library, selected with puromycin, and cultured for 10 population doublings before genomic DNA extraction. sgRNA abundance was quantified at initial and final times by deep sequencing, and data were analyzed using the MAGeCK pipeline. (B) Ranked Robust Rank Aggregation (RRA) scores of the most significantly depleted genes from the screen. (C) Ranked RRA scores of the most significantly enriched genes from the screen. (D) Volcano plot of CRISPR screen results showing significantly depleted genes (blue) versus non-significant genes (gray). The x-axis represents log₂(fold change) (Log₂FC) in sgRNA abundance, and the y-axis shows –log₁₀ P values from MAGeCK analysis. (E) Volcano plot showing significantly enriched genes (red) versus non-significant genes (gray).

    Journal: bioRxiv

    Article Title: Unbiased CRISPR Synthetic Lethal Screening for Genetic Vulnerabilities in Succinate Dehydrogenase (SDH)-loss Model of Paraganglioma

    doi: 10.1101/2025.08.26.672429

    Figure Lengend Snippet: (A) Schematic workflow of the pooled CRISPR/Cas9 gene knockout screen. Cas9-expressing chromaffin cells were generated via lentiviral transduction and blasticidin selection. Cells were then transduced with a genome-wide sgRNA library, selected with puromycin, and cultured for 10 population doublings before genomic DNA extraction. sgRNA abundance was quantified at initial and final times by deep sequencing, and data were analyzed using the MAGeCK pipeline. (B) Ranked Robust Rank Aggregation (RRA) scores of the most significantly depleted genes from the screen. (C) Ranked RRA scores of the most significantly enriched genes from the screen. (D) Volcano plot of CRISPR screen results showing significantly depleted genes (blue) versus non-significant genes (gray). The x-axis represents log₂(fold change) (Log₂FC) in sgRNA abundance, and the y-axis shows –log₁₀ P values from MAGeCK analysis. (E) Volcano plot showing significantly enriched genes (red) versus non-significant genes (gray).

    Article Snippet: Parental imCC lines were made to express Cas9 by transduction with 3 rd generation lentiviral particles carrying codon-optimized S. pyogenes Cas9 protein and blasticidin resistance driven from the EFS promoter (Addgene # 52962-LV).

    Techniques: CRISPR, Gene Knockout, Expressing, Generated, Transduction, Selection, Genome Wide, Cell Culture, DNA Extraction, Sequencing