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Xeroderma Pigmentosum, Complementation Group G (XPG) Polyclonal Antibody

CAT: 0617-CAU25157-01Size: 100 µLDry Ice: NoHazardous: No
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CAT#:0617-CAU25157-01Size:100 µL
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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Description
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.
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
Species
Human (Homo sapiens)

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