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FANCG (Fanconi Anemia Group G Protein, XRCC9, Protein FACG, DNA-repair Protein XRCC9)

FANCG (Fanconi Anemia Group G Protein, XRCC9, Protein FACG, DNA-repair Protein XRCC9)

Cat no: F0019-58W8A

Supplier: United States Biological
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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 622aa 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. Applications: Suitable for use in ELISA, Immunoprecipitation, Immunofluorescence, and Western Blot. Other applications not tested. Recommended Dilution: Optimal dilutions to be determined by the researcher. Storage and Stability: May be stored at 4 degrees C for short-term only. Aliquot to avoid repeated freezing and thawing. Store at -20 degrees C. Aliquots are stable for at least 12 months. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap.
Catalogue number: F0019-58W8A
Reactivities: Human
Hosts: Mouse
Applications: ELISA, Immunofluorescence, Immunoprecipitation, Western Blot
Size: 100ug
Form: Supplied as a liquid in PBS, pH 7.2.
P type: Mab
Isotype: IgG2a,k
Purity: Purified.
References: 1.Four human FANCG polymorphic variants show normal biological function in hamster CHO cells. Hinz JM, Nham PB, Yamada NA, Tebbs RS, Salazar EP, Hinz AK, Mohrenweiser HW, Jones IM, Thompson LH.Mutat Res. 2006 Dec 1;602(1-2):34-42. Epub 2006 Sep 28.
Additional info: Recognizes human FANCG.

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