Background:

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.

Classification:

Primary antibody

Alternative names:

XRCC4; DNA repair protein XRCC4; X-ray repair cross-complementing protein 4

Species reactivity:

Human

Host:

Mouse

Isotype:

IgG

Immunogen:

Synthetic Peptide of XRCC4

Concentration:

1 mg/ml

Molecular weight:

38287

Applications:

WB, IHC-p, IF, ICC, IP

Storage:

-20°C for one year

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