CSB/ERCC6 Antibody

ERCC6, also known as Cockayne syndrome B protein, is involved in DNA repair in response to UV exposure. ERCC6 has been reported to display ATPase and helicase activity and functions as a transcriptional regulator. Mutations in ERCC6 are the cause of Cockayne syndrome type B (CSB), cerebro-oculo-facio-skeletal syndrome type 1 (COFS1), De Sanctis-Cacchione syndrome (DCS), age-related macular degeneration type 5 (ARMD5), and UV-sensitive syndrome (UVS).
ERCC6
ERCC excision repair 6, chromatin remodeling factor
DNA excision repair protein ERCC-6
:  ARMD5 ATP-dependent helicase ERCC6 CKN2 Cockayne syndrome B protein Cockayne syndrome group B protein cockayne syndrome protein CSB COFS COFS1 CSB ERCC6-PGBD3 fusion protein (isoform 1) excision repair cross-complementation group 6 excision repair cross-complementing rodent repair deficiency, complementation group 6 POF11 RAD26 UVSS1 More... Less...
Product
Specifications
Ordering Information
Human
WB, IP
Between 1 and 50
$339
$229
$99
Human
IP
Between 1161 and 1211
$339
$99
Human
Includes: 1 each of A301-345A and A301-347A
$472
Includes: 1 each of A301-345A and A301-347A