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Spécifications
- Antibody type:Primary
- Antigen name:Fanconi Anemia Complementation Group G
- Clonality:Polyclonal
- Gene ID:2189
- Host:Rabbit
- Isotype:IgG
- Reactivity:Human,Rat,Mouse
- Antigen symbol:FANCG
- Conjugation:Cy3®
- ImmunoChemistry:Yes
- Size:100 µL
- Cross adsorption:No
- Form:liquid
- Antigen synonyms:complementing defective|Protein FACG|FANCG_HUMAN.|in Chinese hamster cells 9|DNA repair protein XRCC9|FAG|XRCC9|Fanconi anaemia complementation group G|X ray repair|DNA-repair protein XRCC9
- Storage buffer:Aqueous buffered solution containing 100ug/ml BSA, 50% glycerol and 0.09% sodium azide. Store at 4°C for 12 months.
- Storage temperature:Store at 4°C for 12 months
- Concentration:1 μg/μl
- Shipping temperature:4°C
- Purification:Purified by Protein A
- Cat. no.:10393-070
- Supplier No.:BS-4106R-CY3
Spécifications
A propos de cet article
FANCG, involved in Fanconi anemia, confers resistance to both hygromycin and mitomycin C. FANCG contains a 5-prime GC-rich untranslated region characteristic of housekeeping genes. The putative 622-amino acid protein has a leucine-zipper motif at its N-terminus. Fanconi anemia is an autosomal recessive disorder with diverse clinical symptoms, including developmental anomalies, bone marrow failure, and early occurrence of malignancies. A minimum of 8 FA genes have been identified.
Recommended Dilutions: IF(IHC-P): 1:50-200
Type: Primary
Antigen: FANCG
Clonality: Polyclonal
Clone:
Conjugation: Cy3®
Epitope:
Host: Rabbit
Isotype: IgG
Reactivity: Human, Mouse, Rat