General Transcription And DNA Repair Factor IIH Helicase Subunit XPB (ERCC3) Antibody

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312€ (60 µl)

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935106861
info@markelab.com
name
General Transcription And DNA Repair Factor IIH Helicase Subunit XPB (ERCC3) Antibody
category
Primary Antibodies
provider
Abbexa
reference
abx001433
tested applications
WB

Description

ERCC3 Antibody is a Rabbit Polyclonal antibody against ERCC3. 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.

Documents del producto

Instrucciones
Data sheet
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Product specifications

Category
Primary Antibodies
Immunogen Target
General Transcription And DNA Repair Factor IIH Helicase Subunit XPB (ERCC3)
Host
Rabbit
Reactivity
Human, Mouse, Rat
Recommended Dilution
WB: 1/500 - 1/2000. Optimal dilutions/concentrations should be determined by the end user.
Clonality
Polyclonal
Conjugation
Unconjugated
Isotype
IgG
Purification
Purified by affinity chromatography.
Size 1
60 µl
Size 2
120 µl
Size 3
200 µl
Form
Liquid
Tested Applications
WB
Buffer
PBS, pH 7.3, containing 0.01% thiomersal, 50% glycerol.
Availability
Shipped within 5-10 working days.
Storage
Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles.
Dry Ice
No
UniProt ID
P19447
Gene ID
2071
NCBI Accession
NP_000113.1
Background
Antibody anti-ERCC3
Status
RUO
Note
Concentration: 1 mg/ml - 

Descripción

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General Transcription And DNA Repair Factor IIH Helicase Subunit XPB (ERCC3) Antibody

ERCC3 Antibody is a Rabbit Polyclonal antibody against ERCC3. 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.

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