FAM36A Antikörper (AA 51-118) (Alexa Fluor 594)

Produktnummer ABIN2813081

Produktdetails anti-FAM36A Antikörper

Target: FAM36A (Family with Sequence Similarity 36, Member A (FAM36A))

Bindungsspezifität: AA 51-118

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser FAM36A Antikörper ist konjugiert mit Alexa Fluor 594

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

Homologie: Human

Aufreinigung: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human FAM36A

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.

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

Lagerung: -20 °C/-80 °C

Informationen zur Lagerung: Store at -20°C, for long storage, store at -80°C. Avoid multiple freeze-thaw cycles

Haltbarkeit: 12 months

Details zu FAM36A

Target: FAM36A (Family with Sequence Similarity 36, Member A (FAM36A))

Andere Bezeichnung: FAM36A (FAM36A Produkte)

Synonyme: FAM36A antikoerper, 2310005N03Rik antikoerper, Fam36a antikoerper, RGD1309105 antikoerper, cox20 antikoerper, fam36a antikoerper, COX20, cytochrome c oxidase assembly factor antikoerper, COX20 Cox2 chaperone antikoerper, COX20 cytochrome C oxidase assembly factor antikoerper, COX20 cytochrome c oxidase assembly factor L homeolog antikoerper, COX20 antikoerper, Cox20 antikoerper, cox20.L antikoerper

Hintergrund:

FAM36A is a multi-pass membrane protein. It belongs to the FAM36 family. The exact function of FAM36A remains unknown.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 FAM36A gene product has been provisionally designated FAM36A pending further characterization.

Subcellular location: Cytoplasm

Synonyms: FAM 36A, Family with sequence similarity 36 member A, FLJ43269, Hypothetical protein LOC116228, OTTHUMP00000038200, Protein FAM36A.

Gen-ID: 116228