XLF (NHEJ1) Mouse Monoclonal Antibody [Clone ID: OTI3E5]

CAT#: TA502005S

NHEJ1 (XLF) mouse monoclonal antibody, clone OTI3E5 (formerly 3E5)

Product Images

HEK293T cells were transfected with the pCMV6-ENTRY control (Left lane) or pCMV6-ENTRY NHEJ1 (RC203393, Right lane) cDNA for 48 hrs and lysed. Equivalent amounts of cell lysates (5 ug per lane) were separated by SDS-PAGE and immunoblotted with anti-NHEJ1. Positive lysates LY403031 (100ug) and LC403031 (20ug) can be purchased separately from OriGene.

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  Western blot analysis of extracts (35ug) from 9 different cell lines by using anti-NHEJ1 monoclonal antibody (HepG2: human; HeLa: human; SVT2: mouse; A549: human; COS7: monkey; Jurkat: human; MDCK: canine; PC12: rat; MCF7: human) (1:200).

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  HEK293T cells transfected with either RC203393 overexpress plasmid (Red) or empty vector control plasmid (Blue) were immunostained by anti-NHEJ1 antibody (TA502005), and then analyzed by flow cytometry.

Specifications

Product Data

• Clone Name: OTI3E5
• Applications: FC, WB
• Recommended Dilution: WB 1:2000, Flow: 1:100
• Reactivities: Human
• Host: Mouse
• Isotype: IgG1
• Clonality: Monoclonal
• Immunogen: Full length human recombinant protein of human NHEJ1 (NP_079058) produced in HEK293T cell.
• Formulation: PBS (PH 7.3) containing 1% BSA, 50% glycerol and 0.02% sodium azide.
• Concentration: 0.59 mg/ml
• Purification: Purified from mouse ascites fluids or tissue culture supernatant by affinity chromatography (protein A/G)
• Conjugation: Unconjugated
• Storage: Store at -20°C as received.
• Stability: Stable for 12 months from date of receipt.
• Predicted Protein Size: 33.2 kDa
• Gene Name: non-homologous end joining factor 1
• Database Link:
  NP_079058
  Entrez Gene 79840 Human
  UniProt ID Q9H9Q4
• Background: Double-strand breaks in DNA result from genotoxic stresses and are among the most damaging of DNA lesions. This gene encodes a DNA repair factor essential for the nonhomologous end-joining pathway, which preferentially mediates repair of double-stranded breaks. Mutations in this gene cause different kinds of severe combined immunodeficiency disorders. [provided by RefSeq]
• Synonyms: XLF

Reference Data

• Protein Pathways: Non-homologous end-joining