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Rabbit anti-ERCC3 Antibody, Affinity Purified

Catalog No.
A301-337A-M
Pack Size
  • 20 µl (2 blots)
  • 100 µl (10 blots)
  • 100 µl (1000 µg/ml)
Quantity
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Brand:
Specifications
A301-337A-M
Brand
Bethyl Laboratories
Application
IP
WB
Storage Conditions
2 - 8° C
Host
Rabbit
Conjugation
Unconjugated
Immunogen
between 732 and 782
Buffer
Tris-citrate/phosphate buffer, pH 7 to 8 containing 0.09% Sodium Azide
Reactivity
Human, Mouse
Target
ERCC3
Shelf Life
1 year from date of receipt
Antibody Type
Polyclonal
Alternate Names
basic transcription factor 2 89 kDa subunit, BTF2, BTF2 p89, DNA excision repair protein ERCC-3, DNA repair helicase, DNA repair protein complementing XP-B cells, excision repair cross-complementation group 3, excision repair cross-complementing rodent repair deficiency, complementation group 3, general transcription and DNA repair factor IIH helicase subunit XPB, GTF2H, RAD25, TFIIH, TFIIH 89 kDa subunit, TFIIH basal transcription factor complex 89 kDa subunit, TFIIH basal transcription factor complex helicase XPB subunit, TFIIH p89, TFIIH subunit XPB, TTD2, xeroderma pigmentosum group B-complementing protein, xeroderma pigmentosum, complementation group B, XPB
Format
Whole IgG
Presumed Reactivity
Based on 100% sequence identity, this antibody is predicted to react with Rat, Bovine and Orangutan
Product Type
Primary Antibodies
Product Sub Types
Primary Antibodies
UNSPSC
12352203
Western Blot (WB)
1:2,000 - 1:10,000
Immunoprecipitation (IP)
2 - 5 µg/mg lysate
Target Sentence
ERCC3 is a component of the core TFIIH basal transcription factor and functions as an ATP-dependent 3’-5’ DNA helicase. ERCC3 is involved in nucleotide excision repair and is the cause of xeroderma pigmentosum complementation group B (XPB), also known as xeroderma pigmentosum II (XP2). Additionally, it has been found to be the cuase of Cockayne syndrome, and trichothiodystrophy (TTD). XPB is an autosomal recessive disease characterized by skin photosensitivity and a predisposition to skin cancer, and neurological abnormalities. Cockayne syndrome and TTD are similarly characterized by photosensitivity and neural abnormalities.
Product Link
http://www.bethyl.com/product/A301-337A
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