XRCC4 Protein (Transcript Variant 1) (Myc-DYKDDDDK Tag)

Produktnummer ABIN2735697

Produktdetails

Target: XRCC4 (X-Ray Repair Complementing Defective Repair in Chinese Hamster Cells 4 (XRCC4))

Protein-Typ: Recombinant

Proteineigenschaft: Transcript Variant 1

Spezies: Human

Quelle: HEK-293 Cells

Aufreinigungstag / Konjugat: Dieses XRCC4 Protein ist gelabelt mit Myc-DYKDDDDK Tag.

Applikation: Antibody Production (AbP), Standard (STD)

Produktmerkmale:

• Recombinant human XRCC4 (transcript variant 1) protein expressed in HEK293 cells.
• Produced with end-sequenced ORF clone

Reinheit: > 80 % as determined by SDS-PAGE and Coomassie blue staining

Anwendungsinformationen

Applikationshinweise: Recombinant human proteins can be used for:
Native antigens for optimized antibody production
Positive controls in ELISA and other antibody assays

Kommentare:

The tag is located at the C-terminal.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Konzentration: 50 μg/mL

Buffer: 25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.

Lagerung: -80 °C

Informationen zur Lagerung: Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.

Antigendetails

Target: XRCC4 (X-Ray Repair Complementing Defective Repair in Chinese Hamster Cells 4 (XRCC4))

Andere Bezeichnung: Xrcc4 (XRCC4 Produkte)

Synonyme: zgc:73312 Protein, MGC81443 Protein, homolog of human DNA ligase iv-binding protein XRCC4 Protein, 2310057B22Rik Protein, AW413319 Protein, AW545101 Protein, X-ray repair cross complementing 4 Protein, X-ray repair complementing defective repair in Chinese hamster cells 4 Protein, X-ray repair complementing defective repair in Chinese hamster cells 4 L homeolog Protein, DNA ligase IV-binding protein Protein, XRCC4 Protein, xrcc4 Protein, xrcc4.L Protein, Xrcc4 Protein

Hintergrund: 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.

Molekulargewicht: 37.9 kDa

NCBI Accession: NP_003392

Pathways: DNA Reparatur, Production of Molecular Mediator of Immune Response