Xeroderma Pigmentosum, Complementation Group G (XPG) Polyclonal Antibody

The Xeroderma Pigmentosum, Complementation Group G (XPG) Polyclonal Antibody is applicable for the following applications: WB, ICC, IHC-P, IHC-F, ELISA. Host: Rabbit. Species Reactivity: Human (Homo sapiens), Mouse (Mus musculus), Rat (Rattus norvegicus), Pig (Sus scrofa; Porcine) . Immunogen: Leu778~Ala986. Accession Number: P28715. Gene ID: 2073. Target Synonyms: ERCM2; ERCC5; UVDR; XPGC; Excision Repair Cross-Complementing Rodent Repair Deficiency 5; Cockayne Syndrome; DNA repair protein complementing XP-G cells. Restrictions: For Research Use Only. Not for use in diagnostic procedures.

Product Specifications

CAS Number

9007-83-4

Short Description

The Xeroderma Pigmentosum, Complementation Group G (XPG) Polyclonal Antibody is applicable for the following applications: WB, ICC, IHC-P, IHC-F, ELISA.

Gene ID

2073

Accession Number

P28715

Host

Rabbit

Reactivity

Human (Homo sapiens), Mouse (Mus musculus), Rat (Rattus norvegicus), Pig (Sus scrofa; Porcine)

Immunogen

Leu778~Ala986

Target

Xeroderma Pigmentosum, Complementation Group G (XPG)

Clonality

Polyclonal

Conjugation

Unconjugated. Conjugated antibodies are available (Alexa Fluor 405, Alexa Fluor 488, Alexa Fluor 555, Alexa Fluor 597, Alexa Fluor 647, Alexa Fluor 750, APC, APC-Cy5, APC-Cy7, Biotin, Biotin-APC, Cy3, Cy5, Cy5.5, Cy7, FITC, FITC-Biotin, HRP, PE, PE-Cy3, PE-Cy5, PE-Cy5.5, PE-Cy7, PerCP, PerCP-Cy5.5 and TRITC), please inquire.

Applications

WB, ICC, IHC-P, IHC-F, ELISA

Field of Research

Developmental Science

Purification

Antigen-specific affinity chromatography followed by Protein A affinity chromatography

Concentration

0.5mg/ml

Buffer

0.01M PBS, pH7.4, containing 0.05% Proclin-300, 50% glycerol

Shipping Conditions

Ice packs

Storage Conditions

2°C to 8°C for frequent use, -20°C for 12 months. Avoid repeated freeze/thaw cycles.

Appearance

Liquid

Target Alternative Name

ERCM2; ERCC5; UVDR; XPGC; Excision Repair Cross-Complementing Rodent Repair Deficiency 5; Cockayne Syndrome; DNA repair protein complementing XP-G cells