Use Able AI chat for product recommendations

ERCC8 Polyclonal antibody, PBS Only

ERCC8 Polyclonal Antibody for WB, Indirect ELISA

Cat No. 15921-1-PBS

Host / Isotype

Rabbit / IgG

Reactivity

human, mouse

Applications

WB, Indirect ELISA

CKN1, CSA, DNA excision repair protein ERCC-8, ERCC Excision Repair 8, CSA Ubiquitin Ligase Complex Subunit

Formulation:  PBS Only
Conjugate:  Unconjugated
Size/Concentration: 

-/ -

Freight/Packing: -

Quantity

Please visit your regions distributor:


Product Information

15921-1-PBS targets ERCC8 in WB, Indirect ELISA applications and shows reactivity with human, mouse samples.

Tested Reactivity human, mouse
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen

CatNo: Ag8734

Product name: Recombinant human ERCC8 protein

Source: e coli.-derived, PGEX-4T

Tag: GST

Domain: 1-205 aa of BC009793

Sequence: MLGFLSARQTGLEDPLRLRRAESTRRVLGLELNKDRDVERIHGGGINTLDIEPVEGRYMLSGGSDGVIVLYDLENSSRQSYYTCKAVCSIGRDHPDVHRYSVETVQWYPHDTGMFTSSSFDKTLKVWDTNTLQTADVFNFEETVYSHHMSPVSTKHCLVAVGTRGPKVQLCDLKSGSCSHILQGIFILFQTATTLSKRFNKKKRY

Predict reactive species
Full Name excision repair cross-complementing rodent repair deficiency, complementation group 8
Calculated Molecular Weight 396 aa, 44 kDa
Observed Molecular Weight42 kDa
GenBank Accession NumberBC009793
Gene Symbol ERCC8
Gene ID (NCBI) 1161
RRIDAB_3741872
Conjugate Unconjugated
FormLiquid
Purification MethodAntigen affinity purification
UNIPROT IDQ13216
Storage Buffer PBS only, pH 7.3.
Storage ConditionsStore at -80°C.

Background Information

ERCC8 (also known as Cockayne Syndrome A protein, CSA) is a critical nuclear protein that serves as a specific adapter component of the CRL4ᴱᴿᶜᶜ⁸ ubiquitin ligase complex. Its primary function is to play a central role in the transcription-coupled nucleotide excision repair pathway, specifically recognizing and repairing the template strands of actively transcribed genes damaged by factors such as ultraviolet radiation. Mutations in the ERCC8 gene cause Cockayne syndrome, an autosomal recessive disorder characterized by severe photosensitivity, premature aging, neurodevelopmental abnormalities, and sensorineural hearing loss. This demonstrates that ERCC8 is essential for maintaining transcriptional fidelity, neuronal survival, and combating oxidative stress. Therefore, ERCC8 is not only a key factor in DNA repair but also an important molecule for studying mechanisms of premature aging and neurobiology.

Loading...
||
New chat

Able

正在加载,请稍候...