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Excision Repair Cross-Complementing Rodent Repair Deficiency, Complementation Group 3 (Xeroderma Pigmentosum Group B Complementing) (ERCC3) (N-Term) Peptid

ERCC3 Reaktivität: Human Wirt: Synthetic BP, WB
Produktnummer ABIN976409

Kurzübersicht für Excision Repair Cross-Complementing Rodent Repair Deficiency, Complementation Group 3 (Xeroderma Pigmentosum Group B Complementing) (ERCC3) (N-Term) Peptid (ABIN976409)

Target

ERCC3 (Excision Repair Cross-Complementing Rodent Repair Deficiency, Complementation Group 3 (Xeroderma Pigmentosum Group B Complementing) (ERCC3))

Spezies

Human

Quelle

Synthetic

Applikation

Blocking Peptide (BP), Western Blotting (WB)
  • Protein Region

    N-Term

    Sequenz

    MGKRDRADRD KKKSRKRHYE DEEDDEEDAP GNDPQEAVPS AAGKQVDESG

    Produktmerkmale

    This is a synthetic peptide designed for use in combination with anti-ERCC3 Antibody(ARP37963_P050),. It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.

    Aufreinigung

    Purified
  • Applikationshinweise

    Each Investigator should determine their own optimal working dilution for specific applications.

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Lyophilized

    Rekonstitution

    Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.

    Konzentration

    1 mg/mL

    Buffer

    Final peptide concentration is 1 mg/mL in PBS.

    Handhabung

    Avoid repeated freeze-thaw cycles.

    Lagerung

    -20 °C

    Informationen zur Lagerung

    For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
  • Target

    ERCC3 (Excision Repair Cross-Complementing Rodent Repair Deficiency, Complementation Group 3 (Xeroderma Pigmentosum Group B Complementing) (ERCC3))

    Hintergrund

    ERCC3 is an ATP-dependent DNA helicase that functions in nucleotide excision repair and complements xeroderma pigmentosum group B mutations. It also is the 89 kDa subunit of basal transcription factor 2 (TFIIH) and thus functions in class II transcription.

    Alias Symbols: BTF2, GTF2H, RAD25, TFIIH, XPB

    Protein Interaction Partner: CCND1,IRF1,TAF7,TP53,BCR,CCNH,CDK7,ERCC2,GTF2E1,GTF2E2,GTF2H1,GTF2H2,GTF2H3,GTF2H4,GTF2H5,MNAT1,PSMC5,RAD52,TP53,XPC,ATF7IP,BCR,CCNH,CDK7,ERCC2,ERCC5,GCN1L1,GTF2E1,GTF2E2,GTF2H1,GTF2H2,GTF2H3,GTF2H4,GTF2H5,MNAT1,PSMC5,TP53,XPC,ZSCAN1

    Protein Size: 782

    Molekulargewicht

    89 kDa

    Gen-ID

    2071

    NCBI Accession

    NM_000122, NP_000113

    UniProt

    P19447
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