FAM107A Polyclonal Antibody (E-AB-11213)
For research use only.
Verified Samples |
Verified Samples in IHC: Human liver cancer, Human colon cancer |
Dilution | IHC 1:50-1:200 |
Isotype | IgG |
Host | Rabbit |
Reactivity | Human |
Applications | IHC |
Clonality | Polyclonal |
Immunogen | Recombinant protein of human FAM107A |
Abbre | FAM107A |
Synonyms | DRR1, Down regulated in renal cell carcinoma 1, Down-regulated in renal cell carcinoma 1, Downregulated in renal cell carcinoma, F107A, FAM107A, FLJ30158, FLJ45473, Family with sequence similarity 107, Protein FAM107A, Protein TU3A, TU3A, member A |
Swissprot | |
Cellular Localization | Nucleus. |
Concentration | 0.7 mg/mL |
Buffer | Phosphate buffered solution, pH 7.4, containing 0.05% stabilizer and 50% glycerol. |
Purification Method | Affinity purification |
Research Areas | Cancer, Cell Biology |
Conjugation | Unconjugated |
Storage | Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles. |
Shipping | The product is shipped with ice pack,upon receipt,store it immediately at the temperature recommended. |
background | FAM107B is a 131 amino acid protein that is encoded by a gene that maps to human chromosome 10, which contains over 800 genes and 135 million nucleotides, making up nearly 4.5% of the human genome. PTEN is an important tumor suppressor gene located on chromosome 10 and, when defective, causes a genetic predisposition to cancer development known as Cowden syndrome. The chromosome 10 encoded gene ERCC6 is important for DNA repair and is linked to Cockayne syndrome which is characterized by extreme photosensitivity and premature aging. Tetrahydrobiopterin deficiency and a number of syndromes involving defective skull and facial bone fusion are also linked to chromosome 10. As with most trisomies, trisomy 10 is rare and is deleterious. |
Other Clones
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Other Formats
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Unconjugated
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