Xeroderma Pigmentosum, Complementation Group C (XPC) Antibody

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312€ (60 µl)

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935106861
info@markelab.com
name
Xeroderma Pigmentosum, Complementation Group C (XPC) Antibody
category
Primary Antibodies
provider
Abbexa
reference
abx005805
tested applications
IHC

Description

XPC Antibody is a Rabbit Polyclonal Antibody against XPC.

Documents del producto

Instrucciones
Data sheet
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Product specifications

Category
Primary Antibodies
Immunogen Target
Xeroderma Pigmentosum, Complementation Group C (XPC)
Host
Rabbit
Reactivity
Human
Recommended Dilution
IHC-P: 1/50 - 1/100. Not tested in IHC-F. 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
IHC
Buffer
PBS, pH 7.3, containing 0.02% sodium azide, 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
Q01831
Gene ID
7508
NCBI Accession
NP_004619.3
Background
Antibody anti-XPC
Status
RUO
Note
Concentration: 1 mg/ml -

Descripción

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This gene encodes a component of the nucleotide excision repair (NER) pathway. There are multiple components involved in the NER pathway, including Xeroderma pigmentosum (XP) A-G and V, Cockayne syndrome (CS) A and B, and trichothiodystrophy (TTD) group A, etc. This component, XPC, plays an important role in the early steps of global genome NER, especially in damage recognition, open complex formation, and repair protein complex formation. Mutations in this gene or some other NER components result in Xeroderma pigmentosum, a rare autosomal recessive disorder characterized by increased sensitivity to sunlight with the development of carcinomas at an early age. Alternatively spliced transcript variants have been found for this gene.

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