X-Ray Repair Cross-Complementing Protein 4 (XRCC4) Antibody

195€ (20 µl)
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935106861
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name
X-Ray Repair Cross-Complementing Protein 4 (XRCC4) Antibody
category
Primary Antibodies
provider
Abbexa
reference
abx001409
tested applications
ELISA, WB, IHC, IF/ICC
Description
XRCC4 Antibody is a Rabbit Polyclonal antibody against XRCC4. The protein encoded by this gene functions together with DNA ligase IV and the DNA-dependent protein kinase in the repair of DNA double-strand break by non-homologous end joining and the completion of V(D)J recombination events. The non-homologous end-joining pathway is required both for normal development and for suppression of tumors. This gene functionally complements XR-1 Chinese hamster ovary cell mutant, which is impaired in DNA double-strand breaks produced by ionizing radiation and restriction enzymes. Alternative transcription initiation and alternative splicing generates several transcript variants. [provided by RefSeq, Sep 2008].
Documents del producto
Instrucciones
Data sheet
Product specifications
Category | Primary Antibodies |
Immunogen Target | X-Ray Repair Cross-Complementing Protein 4 (XRCC4) |
Host | Rabbit |
Reactivity | Human, Rat |
Recommended Dilution | ELISA: 1 µg/ml, WB: 1/500 - 1/1000, IHC-P: 1/50 - 1/200, IF/ICC: 1/50 - 1/100. Not tested in IHC-F. Optimal dilutions/concentrations should be determined by the end user. |
Clonality | Polyclonal |
Conjugation | Unconjugated |
Isotype | IgG |
Purification | Purified by affinity chromatography. |
Size 1 | 20 µl |
Size 2 | 100 µl |
Size 3 | 2 × 100 µl |
Form | Liquid |
Tested Applications | ELISA, WB, IHC, IF/ICC |
Buffer | PBS, pH 7.3, containing 0.05% Proclin-300, 50% glycerol. |
Availability | Shipped within 5-10 working days. |
Storage | Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles. |
Dry Ice | No |
UniProt ID | Q13426 |
Gene ID | 7518 |
NCBI Accession | NP_001304941.1 |
Background | Antibody anti-XRCC4 |
Status | RUO |
Note | Concentration: > 0.2 mg/ml - |
Descripción
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The protein encoded by this gene functions together with DNA ligase IV and the DNA-dependent protein kinase in the repair of DNA double-strand breaks. This protein plays a role in both non-homologous end joining and the completion of V(D)J recombination. Mutations in this gene can cause short stature, microcephaly, and endocrine dysfunction (SSMED). Alternative splicing generates several transcript variants.
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