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ERCC3 antibody
ERCC3
Reactivity: Human, Mouse
WB, ELISA, IHC
Host: Rabbit
Polyclonal
unconjugated
Product Details anti-ERCC3 Antibody
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Target
See all ERCC3 Antibodies
ERCC3
(DNA Repair Protein Complementing XP-B Cells (ERCC3))
Reactivity
All reactivities for ERCC3 antibodies
Human, Mouse
Host
All hosts for ERCC3 antibodies
Rabbit
Clonality
All clonalities for ERCC3 antibodies
Polyclonal
Conjugate
All conjugates for ERCC3 antibodies
This ERCC3 antibody is un-conjugated
Application
All applications for ERCC3 antibodies
Western Blotting (WB), ELISA, Immunohistochemistry (IHC)
Purification
Immunogen affinity purified
Purity
≥95 % as determined by SDS-PAGE
Immunogen
excision repair cross-complementing rodent repair deficiency, complementation group 3 (xeroderma pigmentosum group B complementing)
Isotype
IgG
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Discover our top product ERCC3 Primary Antibody
Alternatives
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Application Details
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Application Notes
WB: 1:500 - 1:2000, IHC: 1:50 - 1:200
Restrictions
For Research Use only
Handling
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Format
Liquid
Buffer
PBS with 0.02 % sodium azide and 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.
Storage
-20 °C
Storage Comment
-20°C for 12 months (Avoid repeated freeze / thaw cycles.)
Expiry Date
12 months
Target Details for ERCC3
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Target
ERCC3
(DNA Repair Protein Complementing XP-B Cells (ERCC3))
Alternative Name
ERCC3 (ERCC3 Products )
Synonyms
BTF2 antibody, GTF2H antibody, RAD25 antibody, TFIIH antibody, XPB antibody, BTF2 p89 antibody, Ercc-3 antibody, wu:fc25f08 antibody, ERCC excision repair 3, TFIIH core complex helicase subunit antibody, excision repair cross-complementing rodent repair deficiency, complementation group 3 antibody, excision repair cross-complementation group 3 antibody, ERCC3 antibody, Ercc3 antibody, ercc3 antibody
Background
Synonyms:XPB, XPBC 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.
Molecular Weight
80 kDa
Gene ID
2071
UniProt
P19447
Pathways
DNA Damage Repair
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