Anti-ERCC8 Antibody,

Also for ERCC8 (NM_001007233)

Gene Name	Homo sapiens excision repair cross-complementing rodent repair deficiency, complementation group 8 (ERCC8), transcript variant 2
Synonyms:	CSA, CKN1;CKN1; CSA; Cockayne syndrome WD-repeat protein CSA; DNA excision repair protein ERCC-8; excision repair cross-complementing rodent repair deficiency, complementation group 8
Immunogen	Recombinant protein fragment contain a sequence corresponding to a region within amino acids 1 and 164 of ERCC8(CSA)
Buffer	0.1M Tris, 0.1M Glycine, 10% Glycerol (pH7). 0.01% Thimerosal was added as a preservative.
Clone Name		Isotype	IgG
Species Reactivity	Human, Mouse	Concentration	5.39mg/ml
Purification	Affinity purified by Protein A. (Protein A or G Sepharose)
Guaranteed Application *	WB, IF	Suggested Dilutions	WB:1:500-1:3000; IF:1:100-1:500;
Background	This gene encodes a WD repeat protein, which interacts with Cockayne syndrome type B (CSB) protein and with p44 protein, a subunit of the RNA polymerase II transcription factor IIH. Mutations in this gene have been identified in patients with hereditary disease Cockayne syndrome (CS). CS cells are abnormally sensitive to ultraviolet radiation and are defective in the repair of transcriptionally active genes. [provided by RefSeq]
Related Pathway

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WB Image

Sample (30ug whole cell lysate) A:MOLT4 (anti-ERCC8 antibody diluted at 1:1000)

IF Image

Immunofluorescence analysis of paraformaldehyde-fixed HeLa, using ERCC8(anti-ERCC8 antibody) antibody at 1:200 dilution.

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Anti-ERCC8 Antibody

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