Anti-ERCC8 antibody [EPR9237]
- 20ul selling size
- RabMAb
- Recombinant
- KO Validated
- What is this?
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(16 Publications)
Rabbit Recombinant Monoclonal ERCC8 antibody. Suitable for IP, WB and reacts with Human samples. Cited in 16 publications.
View Alternative Names
CKN1, CSA, ERCC8, DNA excision repair protein ERCC-8, Cockayne syndrome WD repeat protein CSA
- IP
Lab
Immunoprecipitation - Anti-ERCC8 antibody [EPR9237] (AB137033)
Purified ab137033 at 1/80 dilution (2μg) immunoprecipitating ERCC8 in HeLa whole cell lysate.
Lane 1 (input) : HeLa (Human cervix adenocarcinoma epithelial cell) whole cell lysate 10μg
Lane 2 (+) : ab137033 + HeLa whole cell lysate.
Lane 3 (-) : Rabbit monoclonal IgG (ab172730) instead of ab137033 in HeLa whole cell lysate.
VeriBlot for IP Detection Reagent (HRP) (ab131366) (1/5000 dilution) was used for Western blotting.
Blocking Buffer and concentration : 5% NFDM/TBST.
Diluting buffer and concentration : 5% NFDM/TBST.
Observed band size : 44 kDa
All lanes:
Immunoprecipitation - Anti-ERCC8 antibody [EPR9237] (ab137033)
Predicted band size: 44 kDa
false
- WB
Unknown
Western blot - Anti-ERCC8 antibody [EPR9237] (AB137033)
Lane 1 : Wild-type HAP1 cell lysate (20 μg)
Lane 2 : ERCC8 knockout HAP1 cell lysate (20 μg)
Lane 3 : HeLa cell lysate (20 μg)
Lane 4 : Molt-4 cell lysate (20 μg)
Lanes 1 - 4 : Merged signal (red and green). Green - ab137033 observed at 44 kDa. Red - loading control, ab8245, observed at 37 kDa.
ab137033 was shown to recognize ERCC8 when ERCC8 knockout samples were used, along with additional cross-reactive bands. Wild-type and ERCC8 knockout samples were subjected to SDS-PAGE. ab137033 and ab8245 (loading control to GAPDH) were diluted 1/1000 and 1/2000 respectively, and incubated overnight at 4°C. Blots were developed with Goat anti-Rabbit IgG H&L (IRDye® 800CW) preadsorbed (ab216773) and Goat anti-Mouse IgG H&L (IRDye® 680RD) preadsorbed (ab216776) secondary antibodies at 1/10 000 dilution for 1 h at room temperature before imaging.
All lanes:
Western blot - Anti-ERCC8 antibody [EPR9237] (ab137033)
Predicted band size: 44 kDa
false
- WB
Unknown
Western blot - Anti-ERCC8 antibody [EPR9237] (AB137033)
All lanes:
Western blot - Anti-ERCC8 antibody [EPR9237] (ab137033) at 1/1000 dilution
Lane 1:
MOLT-4 (Human lymphoblastic leukemia T lymphoblast) whole cell lysate at 15 µg
Lane 2:
293T (Human embryonic kidney epithelial cell) whole cell lysate at 15 µg
Lane 3:
HepG2 (Human hepatocellular carcinoma epithelial cell) whole cell lysate at 15 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/5000 dilution
Predicted band size: 44 kDa
false
Related conjugates and formulations (1)
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Anti-ERCC8 antibody [EPR9237] - BSA and Azide free
Reactivity data
Product details
Species reactivity
Mouse, Rat: We have preliminary internal testing data to indicate this antibody may not react with these species.
Please contact us for more information.
Patented technology
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
What are the advantages of a recombinant monoclonal antibody?
This product is a recombinant monoclonal antibody, which offers several advantages including:
- - High batch-to-batch consistency and reproducibility
- - Improved sensitivity and specificity
- - Long-term security of supply
- - Animal-free batch production
For more information, read more on recombinant antibodies.
Properties and storage information
Form
Purification technique
Storage buffer
Shipped at conditions
Appropriate short-term storage duration
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Aliquoting information
Storage information
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
ERCC8 forms a part of the CSA complex which includes other proteins involved in the TC-NER pathway. The CSA complex targets the repair machinery to the site of transcription-blocking lesions. Identifying these lesions is critical to resuming normal transcription processes. The CSA protein therefore actively contributes to maintaining genomic stability by facilitating the correction of transcription-coupled DNA damage.
Pathways
ERCC8 participates directly in the nucleotide excision repair (NER) pathway specifically in its transcription-coupled repair subprocess. This pathway is integral to correcting helix-distorting DNA lesions that impede transcription. ERCC8 interacts closely with the Cockayne syndrome B (CSB) protein and RNA polymerase II during the repair process. This collaboration is important in modulating the restart of transcription post-repair.
Product protocols
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Target data
Publications (16)
Recent publications for all applications. Explore the full list and refine your search
Cell death and differentiation : PubMed40374849
2025
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Nucleic acids research 53: PubMed40219966
2025
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Frontiers in oncology 14:1476100 PubMed39582530
2024
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Nature communications 15:7089 PubMed39154022
2024
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Cell reports methods 4:100674 PubMed38176411
2024
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Nucleic acids research 51:6238-6245 PubMed37144462
2023
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Cells 11: PubMed36231052
2022
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Nature communications 13:974 PubMed35190564
2022
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Cell 180:1228-1244.e24 PubMed32142649
2020
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Nucleic acids research 48:2473-2485 PubMed31970402
2020
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Product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
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