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ERCC3 antibody (AA 513-782)

The Rabbit Polyclonal anti-ERCC3 antibody has been validated for WB. It is suitable to detect ERCC3 in samples from Human.
Catalog No. ABIN3022427

Quick Overview for ERCC3 antibody (AA 513-782) (ABIN3022427)

Target

See all ERCC3 Antibodies
ERCC3 (DNA Repair Protein Complementing XP-B Cells (ERCC3))

Reactivity

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Human

Host

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Rabbit

Clonality

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Polyclonal

Conjugate

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This ERCC3 antibody is un-conjugated

Application

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Western Blotting (WB)
  • Binding Specificity

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    AA 513-782

    Sequence

    PMSPEFYREY VAIKTKKRIL LYTMNPNKFR ACQFLIKFHE RRNDKIIVFA DNVFALKEYA IRLNKPYIYG PTSQGERMQI LQNFKHNPKI NTIFISKVGD TSFDLPEANV LIQISSHGGS RRQEAQRLGR VLRAKKGMVA EEYNAFFYSL VSQDTQEMAY STKRQRFLVD QGYSFKVITK LAGMEEEDLA FSTKEEQQQL LQKVLAATDL DAEEEVVAGE FGSRSSQASR RFGTMSSMSG ADDTVYMEYH SSRSKAPSKH VHPLFKRFRK

    Cross-Reactivity

    Human, Mouse

    Characteristics

    Polyclonal Antibodies

    Purification

    Affinity purification

    Immunogen

    Recombinant fusion protein containing a sequence corresponding to amino acids 513-782 of human ERCC3 (NP_000113.1).

    Isotype

    IgG
  • Application Notes

    WB,1:500 - 1:2000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

    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 freeze / thaw cycles

    Storage

    -20 °C

    Storage Comment

    Store at -20°C. Avoid freeze / thaw cycles.
  • Target

    ERCC3 (DNA Repair Protein Complementing XP-B Cells (ERCC3))

    Alternative Name

    ERCC3

    Background

    This gene encodes an ATP-dependent DNA helicase that functions in nucleotide excision repair. The encoded protein is a subunit of basal transcription factor 2 (TFIIH) and, therefore, also functions in class II transcription. Mutations in this gene are associated with Xeroderma pigmentosum B, Cockayne's syndrome, and trichothiodystrophy. Alternative splicing results in multiple transcript variants.,ERCC3,BTF2,GTF2H,RAD25,TFIIH,TTD2,XPB,Epigenetics & Nuclear Signaling,Transcription Factors,DNA Damage & Repair,Cancer,Cell Biology & Developmental Biology,Apoptosis,Endocrine & Metabolism,Nucleotide metabolism,Purine and pyrimidine synthesis,ERCC3

    Molecular Weight

    89 kDa

    Gene ID

    2071

    UniProt

    P19447

    Pathways

    DNA Damage Repair
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