CRISPR-Cas9 SP (6C1) Monoclonal Antibody

$Lane 1: 293 cells lysates transfected with CRISPR-Cas9; Lane 2: 293T cells lysates transfected with CRISPR-Cas9; Probed with CRISPR-Cas9 SP (6C1) Monoclonal Antibody (bsm-52960R) at 1:500 overnight at 4\u00b0C followed by a conjugated secondary antibody for 60 minutes at 37\u00b0C.\r\n$

Lane 1: 293 cells lysates transfected with CRISPR-Cas9; Lane 2: 293T cells lysates transfected with CRISPR-Cas9; Probed with CRISPR-Cas9 SP (6C1) Monoclonal Antibody (bsm-52960R) at 1:500 overnight at 4\u00b0C followed by a conjugated secondary antibody for 60 minutes at 37\u00b0C.\r\n

$Lane 1: Recombinant CRISPR-Cas9 protein, C-His (bs-41498P) probed with CRISPR-Cas9 Monoclonal Antibody, Unconjugated (bsm-52960R) at 1:1000 dilution and 4\u00b0C overnight incubation. Followed by conjugated secondary antibody incubation at 1:20000 for 60 min at 37˚C.$

Lane 1: Recombinant CRISPR-Cas9 protein, C-His (bs-41498P) probed with CRISPR-Cas9 Monoclonal Antibody, Unconjugated (bsm-52960R) at 1:1000 dilution and 4\u00b0C overnight incubation. Followed by conjugated secondary antibody incubation at 1:20000 for 60 min at 37˚C.

Applications

Reactivity

Human
Others

Overview
Catalog #	bsm-52960R
Product Name	CRISPR-Cas9 SP (6C1) Monoclonal Antibody
Applications	WB
Reactivity	Human, Others
Specifications
Conjugation	Unconjugated
Host	Rabbit
Source	CRISPR-Cas9 between 700-1100 amino acids
Clonality	Monoclonal
Clone #	6C1
Isotype	IgG
Concentration	1ug/ul
Purification	Purified by Protein A.
Storage Buffer	0.01M TBS(pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
Storage Condition	Store at -20°C for 12 months.
Target
Gene ID	901176
Swiss Prot	Q99ZW2
Synonyms	CRISPR-associated endonuclease Cas9/Csn1, SpCas9, SpyCas9, cas9
Background	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) (PubMed:21455174). 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; Cas9 only stabilizes the pre-crRNA:tracrRNA interaction and has no catalytic function in RNA processing (PubMed:24270795). 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). The target strand not complementary to crRNA is first cut endonucleolytically, then trimmed 3'-5' exonucleolytically. DNA-binding requires protein and both gRNAs, as does nuclease activity. 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. DNA strand separation and heteroduplex formation starts at PAM sites; PAM recognition is required for catalytic activity (PubMed:24476820). Confers immunity against a plasmid with homology to the appropriate CRISPR spacer sequences (CRISPR interference) (PubMed:21455174).
Application Dilution
WB	1:300-5000

Applications

Reactivity

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