![ICC/IF analysis of HeLa cells transiently transfected with flag-tagged Cas9 using Cas9 antibody [7A9] at a dilution of 0.5 microg/ml (green) and DAPI (blue). ICC/IF analysis of HeLa cells transiently transfected with flag-tagged Cas9 using Cas9 antibody [7A9] at a dilution of 0.5 microg/ml (green) and DAPI (blue).](https://www.genetex.com/upload/website/prouct_img/normal/GTX53807/GTX53807_ICCIF_w_23060900_242.webp)
ICC/IF analysis of HeLa cells transiently transfected with flag-tagged Cas9 using Cas9 antibody [7A9] at a dilution of 0.5 microg/ml (green) and DAPI (blue).
Cas9 antibody [7A9]
GTX53807
ApplicationsImmunoFluorescence, ImmunoPrecipitation, Western Blot, ImmunoCytoChemistry
Product group Antibodies
Targetcas9
Overview
- SupplierGeneTex
- Product NameCas9 antibody [7A9]
- Delivery Days Customer9
- Application Supplier NoteWestern Blotting Analysis: 0.5 microg/mL from a representative lot detected Cas9 in 1 microg of Myc-Cas9 expressing HEK293 cell lysate. Immunoprecipitation Analysis: A representative lot immunoprecipitated Cas9 in Flag-Cas9 and Myc-Cas9 expressing cell lysate (performed by an independent laboratory).
- ApplicationsImmunoFluorescence, ImmunoPrecipitation, Western Blot, ImmunoCytoChemistry
- CertificationResearch Use Only
- ClonalityMonoclonal
- Clone ID7A9
- ConjugateUnconjugated
- Gene ID901176
- Target namecas9
- Target descriptiontype II CRISPR RNA-guided endonuclease Cas9
- Target synonymsSPY_RS04360, SPy1046, SPy_1046, type II CRISPR RNA-guided endonuclease Cas9
- HostMouse
- IsotypeIgG1
- Storage Instruction2°C to 8°C
- UNSPSC12352203
References
- Zhao C, Liu H, Xiao T, et al. CRISPR screening of porcine sgRNA library identifies host factors associated with Japanese encephalitis virus replication. Nat Commun. 2020,11(1):5178. doi: 10.1038/s41467-020-18936-1Read this paper
- Shen CC, Hsu MN, Chang CW, et al. Synthetic switch to minimize CRISPR off-target effects by self-restricting Cas9 transcription and translation. Nucleic Acids Res. 2019,47(3):e13. doi: 10.1093/nar/gky1165Read this paper
- Germano G, Lamba S, Rospo G, et al. Inactivation of DNA repair triggers neoantigen generation and impairs tumour growth. Nature. 2017,552(7683):116-120. doi: 10.1038/nature24673Read this paper
- Guo J, Ma D, Huang R, et al. An inducible CRISPR-ON system for controllable gene activation in human pluripotent stem cells. Protein Cell. 2017,8(5):379-393. doi: 10.1007/s13238-016-0360-8Read this paper
![IP analysis was performed with lysate from HEK293T cells expressing Flag-tagged S. pyogenes Cas9 and either Cas9 antibody [7A9] followed by incubation with a 1:1 mixture of protein A/G sepharose beads (Cas9 Sup) or Cas9 antibody [7A9] crosslinked with a 1:1 mixture of protein A/G sepharose beads (Cas9 X-link). The precipitates were detected by the same antibody. Asterisk indicates IgG heavy chain. IP analysis was performed with lysate from HEK293T cells expressing Flag-tagged S. pyogenes Cas9 and either Cas9 antibody [7A9] followed by incubation with a 1:1 mixture of protein A/G sepharose beads (Cas9 Sup) or Cas9 antibody [7A9] crosslinked with a 1:1 mixture of protein A/G sepharose beads (Cas9 X-link). The precipitates were detected by the same antibody. Asterisk indicates IgG heavy chain.](https://www.genetex.com/upload/website/prouct_img/normal/GTX53807/GTX53807_IP_w_23060900_531.webp)



