ERCC6 Recombinant antibody

ERCC6 Uni-rAbTM Recombinant Antibody for WB, ELISA

Cat No. 86144-1-RR
Clone No.250645D4

Host / Isotype

Rabbit / IgG

Reactivity

human

Applications

WB, ELISA

ARMD5, ATP dependent helicase ERCC6, Chimeric CSB-PGBD3 protein, Chimeric ERCC6-PGBD3 protein, CKN2

Formulation:  PBS and Azide
PBS and Azide
PBS Only
Conjugate:  Unconjugated
Unconjugated
Size/Concentration: 

-/ -

Freight/Packing: -

Quantity

Please visit your regions distributor:


Tested Applications

Positive WB detected inHeLa cells

Recommended dilution

ApplicationDilution
Western Blot (WB)WB : 1:500-1:2000
It is recommended that this reagent should be titrated in each testing system to obtain optimal results.
Sample-dependent, Check data in validation data gallery.

Product Information

86144-1-RR targets ERCC6 in WB, ELISA applications and shows reactivity with human samples.

Tested Reactivity human
Host / Isotype Rabbit / IgG
Class Recombinant
Type Antibody
Immunogen ERCC6 fusion protein Ag18009 Predict reactive species
Full Name excision repair cross-complementing rodent repair deficiency, complementation group 6
Calculated Molecular Weight 1493 aa, 168 kDa
Observed Molecular Weight180 kDa
GenBank Accession NumberBC127104
Gene Symbol ERCC6/CSB
Gene ID (NCBI) 2074
Conjugate Unconjugated
Form Liquid
Purification MethodProtein A purification
UNIPROT IDP0DP91
Storage Buffer PBS with 0.02% sodium azide and 50% glycerol, pH 7.3.
Storage ConditionsStore at -20°C. Stable for one year after shipment. Aliquoting is unnecessary for -20oC storage. 20ul sizes contain 0.1% BSA.

Background Information

ERCC6, also named as CSB, belongs to the SNF2/RAD54 helicase family. It is involved in the preferential repair of active genes. It is presumed DNA or RNA unwinding function. ERCC6 corrects the UV survival and RNA synthesis after UV exposure of Cockayne syndrome complementation group B. Defects in ERCC6 are the cause of Cockayne syndrome type B (CSB) , cerebro-oculo-facio-skeletal syndrome type 1 (COFS1), De Sanctis-Cacchione syndrome (DSC), and UV-sensitive syndrome (UVS). Genetic variation in ERCC6 is associated with susceptibility to age-related macular degeneration type 5 (ARMD5). The antibody is specific to ERCC6.

Protocols

Product Specific Protocols
WB protocol for ERCC6 antibody 86144-1-RRDownload protocol
Standard Protocols
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