FAM63A Antikörper (AbBy Fluor® 680)
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- Target Alle FAM63A Antikörper anzeigen
- FAM63A (Family with Sequence Similarity 63, Member A (FAM63A))
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Reaktivität
- Human, Maus, Ratte
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Wirt
- Kaninchen
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Klonalität
- Polyklonal
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Konjugat
- Dieser FAM63A Antikörper ist konjugiert mit AbBy Fluor® 680
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Applikation
- Western Blotting (WB)
- Kreuzreaktivität
- Human, Maus
- Homologie
- Rat,Cow,Sheep,Pig,Horse,Rabbit
- Aufreinigung
- Purified by Protein A.
- Immunogen
- KLH conjugated synthetic peptide derived from human FAM63A
- Isotyp
- IgG
- Top Product
- Discover our top product FAM63A Primärantikörper
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- Applikationshinweise
- IF(IHC-P) 1:50-200
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Format
- Liquid
- Konzentration
- 1 μg/μL
- Buffer
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
- Lagerung
- -20 °C
- Informationen zur Lagerung
- Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
- Haltbarkeit
- 12 months
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- Target
- FAM63A (Family with Sequence Similarity 63, Member A (FAM63A))
- Andere Bezeichnung
- FAM63A (FAM63A Produkte)
- Synonyme
- RP11-316M1.5 antikoerper, 1810005H09Rik antikoerper, 4930504E06Rik antikoerper, AA562754 antikoerper, AA960384 antikoerper, AW561904 antikoerper, cI-40 antikoerper, mKIAA1390 antikoerper, ni antikoerper, si:ch211-210h11.5 antikoerper, MINDY lysine 48 deubiquitinase 1 antikoerper, MINDY1 antikoerper, Mindy1 antikoerper, mindy1 antikoerper
- Hintergrund
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Synonyms: FA63A_HUMAN, FAM 63A, FAM63A, Family with sequence similarity 63 member A, FLJ11280, FLJ43504, Hypothetical protein LOC55793, KIAA1390, Protein FAM63A.
Background: Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8 % of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma. The FAM63A gene product has been provisionally designated FAM63A pending further characterization.
- Gen-ID
- 55793
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