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Anti-CRISPR-Cas9 Rabbit Monoclonal Antibody

     
  • 1 - Anti-CRISPR-Cas9 Rabbit Monoclonal Antibody ABO14108
    Western blot analysis of CRISPR-Cas9 SA expression in (1) 293T cell lysate transfected with CRISPR-Cas9 SA; (2) 293T cell lysate; (3) 3T3 cell lysate; (4) PC12 cell lysate.
  • 3 - Anti-CRISPR-Cas9 Rabbit Monoclonal Antibody ABO14108
    Immunofluorescent analysis of 293T cells transfected with CRISPR-Cas9 SA, using CRISPR-Cas9 SA Antibody.
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Product Information
Application
  • Applications Legend:
  • E=ELISA
  • WB=Western Blotting
  • IHC=Immunohistochemistry
  • IHC-P=Immunohistochemistry (Paraffin)
  • IP=Immunoprecipitation
  • IF=Immunofluorescence
  • IC=Immunochemistry
  • ICC=Immunocytochemistry
  • FC=Flow Cytometry
  • DB=Dot Blot
WB, IHC, IF, ICC, IP, FC
Primary Accession J7RUA5
Host Rabbit
Isotype Rabbit IgG
Clonality Monoclonal
Format Liquid
Description Anti-CRISPR-Cas9 Rabbit Monoclonal Antibody . Tested in WB, IHC, ICC/IF, IP, Flow Cytometry applications. This antibody reacts with Recombinant fragment, Staphylococcus aureus.
Additional Information
Other Names CRISPR-associated endonuclease Cas9 {ECO:0000255|HAMAP-Rule:MF_01480}, 3.1.-.- {ECO:0000255|HAMAP-Rule:MF_01480}, SaCas9, cas9 {ECO:0000255|HAMAP-Rule:MF_01480}
Calculated MW 123949 Da
Application Details WB 1:1000-1:5000
IHC 1:50-1:200
ICC/IF 1:50-1:200
IP 1:30
FC 1:50
Source Bacteria
Contents Rabbit IgG in phosphate buffered saline, pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol, 0.4-0.5mg/ml BSA.
Clone Names Clone: ABCH-3
Immunogen Recombinant fragment derived from Staphylococcus aureus.
Purification Affinity-chromatography
Storage Store at -20°C for one year. For short term storage and frequent use, store at 4°C for up to one month. Avoid repeated freeze-thaw cycles.

For Research Use Only. Not For Use In Diagnostic Procedures.

Protein Information
Name cas9 {ECO:0000255|HAMAP-Rule:MF_01480}
Function CRISPR (clustered regularly interspaced short palindromic repeat) is an adaptive immune system that provides protection against mobile genetic elements (viruses, transposable elements and conjugative plasmids). CRISPR clusters contain spacers, sequences complementary to antecedent mobile elements, and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). In type II CRISPR systems correct processing of pre-crRNA requires a trans- encoded small RNA (tracrRNA), endogenous ribonuclease 3 (rnc) and this protein. The tracrRNA serves as a guide for ribonuclease 3-aided processing of pre-crRNA. Subsequently Cas9/crRNA/tracrRNA endonucleolytically cleaves linear or circular dsDNA target complementary to the spacer; Cas9 is inactive in the absence of the 2 guide RNAs (gRNA). Cas9 recognizes the protospacer adjacent motif (PAM) in the CRISPR repeat sequences to help distinguish self versus nonself, as targets within the bacterial CRISPR locus do not have PAMs. PAM recognition is also required for catalytic activity.
Research Areas
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