FAM107A Antikörper
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- Target Alle FAM107A Antikörper anzeigen
- FAM107A (Family with Sequence Similarity 107, Member A (FAM107A))
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Reaktivität
- Human
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Wirt
- Kaninchen
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Klonalität
- Polyklonal
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Konjugat
- Dieser FAM107A Antikörper ist unkonjugiert
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Applikation
- ELISA, Immunohistochemistry (IHC)
- Produktmerkmale
- Polyclonal Antibody
- Aufreinigung
- Affinity purification
- Immunogen
- Recombinant protein of human FAM107A
- Isotyp
- IgG
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- Applikationshinweise
- IHC 1:50-1:200
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Format
- Liquid
- Konzentration
- 0.7 mg/mL
- Buffer
- PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
- Konservierungsmittel
- Sodium azide
- Vorsichtsmaßnahmen
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Lagerung
- -20 °C
- Informationen zur Lagerung
- Store at -20°C. Avoid freeze / thaw cycles.
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- Target
- FAM107A (Family with Sequence Similarity 107, Member A (FAM107A))
- Andere Bezeichnung
- FAM107A (FAM107A Produkte)
- Synonyme
- drr1 antikoerper, tu3a antikoerper, xdrr1 antikoerper, DRR1 antikoerper, TU3A antikoerper, Drr1 antikoerper, RGD1306327 antikoerper, Tu3a antikoerper, family with sequence similarity 107 member A S homeolog antikoerper, family with sequence similarity 107 member A antikoerper, family with sequence similarity 107, member A antikoerper, fam107a.S antikoerper, FAM107A antikoerper, Fam107a antikoerper
- Hintergrund
- 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.
- UniProt
- O95990
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