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You are here:Home » Antibodies » Antibodies-Fanconi Proteins » Anti -Fanconi anemia G (Fanconi anemia Group G-Protein, Protein FACG, DNA-repair protein XRCC9)

Anti -Fanconi anemia G (Fanconi anemia Group G-Protein, Protein FACG, DNA-repair protein


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Clone Host Grade Applications
Polyclonal Rabbit B
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.
Catalog #F0019-58W8
Cellular Localization The major form is nuclear. The minor form is cytoplasmic.
ApplicationsSuitable for use in Western Blot. Other applications not tested.
Recommended DilutionOptimal dilutions to be determined by the researcher.
Storage and StabilityMay be stored at 4°C for short-term only. For long-term storage and to avoid repeated freezing and thawing, aliquot Store at -20°C. Aliquots are stable for at least 12 months at -20°C. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Further dilutions can be made in assay buffer.
Clone TypePolyclonal
ConcentrationNot determined
FormAs reported
PurityWhole antisera
ImmunogenA C-Terminal peptide within residues 550- 622 of 622. Homology: 100% homology with human protein.
88% homology with mouse protein.
SpecificitySpecies Crossreactivity: This antibody reacts with the human protein.
Important NoteThis product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications without the expressed written authorization of United States Biological.
Alternate namesFanconi anemia Group G Protein, Protein FACG, DNA-repair protein XRCC9

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