FAM102B Antikörper (AA 53-150) (Cy5)

Produktnummer ABIN896112

Produktdetails anti-FAM102B Antikörper (Cy5)

Target: FAM102B (Family with Sequence Similarity 102, Member B (FAM102B))

Bindungsspezifität: AA 53-150

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser FAM102B Antikörper ist konjugiert mit Cy5

Applikation: Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))

Kreuzreaktivität: Human

Homologie: Mouse,Rat,Dog,Cow,Sheep,Pig,Horse,Rabbit

Aufreinigung: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human FAM102B

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

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.

Konservierungsmittel: ProClin

Vorsichtsmaßnahmen: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

Lagerung: -20 °C

Informationen zur Lagerung: Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Haltbarkeit: 12 months

Details zu FAM102B

Target: FAM102B (Family with Sequence Similarity 102, Member B (FAM102B))

Andere Bezeichnung: FAM102B (FAM102B Produkte)

Synonyme: SYM-3B antikoerper, 1600010D10Rik antikoerper, B430201A12Rik antikoerper, RGD1310037 antikoerper, si:ch211-199m3.7 antikoerper, fam102b antikoerper, zgc:136846 antikoerper, family with sequence similarity 102 member B antikoerper, family with sequence similarity 102, member B antikoerper, family with sequence similarity 102, member B, b antikoerper, family with sequence similarity 102, member B, a antikoerper, FAM102B antikoerper, Fam102b antikoerper, fam102bb antikoerper, fam102ba antikoerper

Hintergrund:

Synonyms: F102B_HUMAN, Fam102b, Protein FAM102B.

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 FAM102B gene product has been provisionally designated FAM102B pending further characterization.

Gen-ID: 284611