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ERCC2 antibody (N-Term)

ERCC2 Reactivity: Human, Mouse, Rat, Guinea Pig, Cow, Zebrafish (Danio rerio) WB Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN504641
  • Target See all ERCC2 Antibodies
    ERCC2 (Excision Repair Cross-Complementing Rodent Repair Deficiency, Complementation Group 2 (ERCC2))
    Binding Specificity
    • 5
    • 4
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    N-Term
    Reactivity
    • 40
    • 18
    • 14
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Human, Mouse, Rat, Guinea Pig, Cow, Zebrafish (Danio rerio)
    Host
    • 34
    • 6
    Rabbit
    Clonality
    • 34
    • 6
    Polyclonal
    Conjugate
    • 33
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This ERCC2 antibody is un-conjugated
    Application
    • 29
    • 10
    • 10
    • 7
    • 3
    • 2
    • 2
    • 1
    • 1
    Western Blotting (WB)
    Sequence
    KLNVDGLLVY FPYDYIYPEQ FSYMRELKRT LDAKGHGVLE MPSGTGKTVS
    Cross-Reactivity
    Cow (Bovine), Fruit Fly (Drosophila melanogaster), Human, Mouse (Murine), Pig (Porcine), Rat (Rattus)
    Predicted Reactivity
    Cow: 100%, Guinea Pig: 100%, Human: 100%, Mouse: 100%, Rat: 100%, Zebrafish: 100%
    Characteristics
    This is a rabbit polyclonal antibody against ERCC2. It was validated on Western Blot using a cell lysate as a positive control.
    Purification
    Affinity Purified
    Immunogen
    The immunogen is a synthetic peptide directed towards the N terminal region of human ERCC2
    Top Product
    Discover our top product ERCC2 Primary Antibody
  • Application Notes
    WB Suggested Anti-ERCC2 Antibody Titration: 0.2-1 µg/mL
    ELISA Titer: 1:312500
    Positive Control: Human Muscle.
    Optimal working dilutions should be determined experimentally by the investigator.
    Comment

    Antigen size: 760 AA

    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    Lot specific
    Buffer
    Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.
    Preservative
    Sodium azide
    Precaution of Use
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Handling Advice
    Avoid repeated freeze-thaw cycles.
    Storage
    -20 °C
    Storage Comment
    For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
  • Target
    ERCC2 (Excision Repair Cross-Complementing Rodent Repair Deficiency, Complementation Group 2 (ERCC2))
    Alternative Name
    ERCC2 (ERCC2 Products)
    Synonyms
    COFS2 antibody, EM9 antibody, TTD antibody, XPD antibody, AA407812 antibody, AU020867 antibody, AW240756 antibody, CXPD antibody, Ercc-2 antibody, MGC89573 antibody, CG9433 antibody, DhR3 antibody, DhXPD antibody, DmXPD antibody, Dmel\\CG9433 antibody, ERCC2 antibody, XPD/ERCC2 antibody, l(2)SH2 2137 antibody, l(2)SH2137 antibody, xpd antibody, zgc:56365 antibody, ERCC excision repair 2, TFIIH core complex helicase subunit antibody, excision repair cross-complementing rodent repair deficiency, complementation group 2 antibody, excision repair cross-complementation group 2 antibody, Xeroderma pigmentosum D antibody, ERCC2 antibody, Ercc2 antibody, ercc2 antibody, Xpd antibody
    Background
    The nucleotide excision repair pathway is a mechanism to repair damage to DNA. ERCC2 is involved in transcription-coupled nucleotide excision repair and is an integral member of the basal transcription factor BTF2/TFIIH complex. This protein has ATP-dependent DNA helicase activity and belongs to the RAD3/XPD subfamily of helicases. Defects in this gene can result in three different disorders, the cancer-prone syndrome xeroderma pigmentosum complementation group D, trichothiodystrophy, and Cockayne syndrome. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. The nucleotide excision repair pathway is a mechanism to repair damage to DNA. The protein encoded by this gene is involved in transcription-coupled nucleotide excision repair and is an integral member of the basal transcription factor BTF2/TFIIH complex. The gene product has ATP-dependent DNA helicase activity and belongs to the RAD3/XPD subfamily of helicases. Defects in this gene can result in three different disorders, the cancer-prone syndrome xeroderma pigmentosum complementation group D, trichothiodystrophy, and Cockayne syndrome. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.
    Alias Symbols: COFS2, EM9, MGC102762, MGC126218, MGC126219, TTD, XPD
    Protein Interaction Partner: GTF2H2C_2, UBC, FAM96B, CIAO1, rev, CDK7, TP53, MMS19, ERCC3, UVSSA, RAD52, GTF2H1, MNAT1, CCNH, GTF2F1, PIDD1, GTF2H3, GTF2H2, AR, ERCC6, tat, ATF7IP, HERC5, ISG15, TRIM25, RAD51, ERCC5, ERCC2, CDK1,
    Protein Size: 760
    Molecular Weight
    87 kDa
    Gene ID
    2068
    NCBI Accession
    NM_000400, NP_000391
    UniProt
    P18074
    Pathways
    DNA Damage Repair
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