VAT1L Antikörper (AA 321-419) (Biotin)

Produktnummer ABIN1389451

Produktdetails anti-VAT1L Antikörper (Biotin)

Target: VAT1L (Vesicle Amine Transport 1-Like (VAT1L))

Bindungsspezifität: AA 321-419

Reaktivität: Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser VAT1L Antikörper ist konjugiert mit Biotin

Applikation: Western Blotting (WB), ELISA, Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Kreuzreaktivität: Ratte

Homologie: Human,Mouse,Dog,Cow,Pig

Aufreinigung: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human VAT1L/KIAA1576

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB 1:300-5000
IHC-P 1:200-400
IHC-F 1:100-500

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 for 12 months.

Haltbarkeit: 12 months

Details zu VAT1L

Target: VAT1L (Vesicle Amine Transport 1-Like (VAT1L))

Andere Bezeichnung: VAT1L/KIAA1576 (VAT1L Produkte)

Synonyme: VAT1L antikoerper, 9430073I07 antikoerper, AI427515 antikoerper, mKIAA1576 antikoerper, zgc:171879 antikoerper, vesicle amine transport 1 like antikoerper, vesicle amine transport protein 1 like antikoerper, vesicle amine transport 1-like antikoerper, VAT1L antikoerper, Vat1l antikoerper, vat1l antikoerper

Hintergrund:

Synonyms: Probable oxidoreductase KIAA1576, Synaptic vesicle membrane protein VAT 1 homolog like, Synaptic vesicle membrane protein VAT-1 homolog-like, VAT 1L, VAT1L, VAT1L_HUMAN, Vesicle amine transport protein 1 homolog T. calornica like.

Background: Chromosome 16 encodes over 900 genes in approximately 90 million base pairs, makes up nearly 3 % of human cellular DNA and is associated with a variety of genetic disorders. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16, though through the CREBBP gene which encodes a critical CREB binding protein. Signs of Rubinstein-Taybi include mental retardation and predisposition to tumor growth and white blood cell neoplasias. Crohn's disease is a gastrointestinal inflammatory condition associated with chromosome 16 through the NOD2 gene. An association with systemic lupus erythematosis and a number of other autoimmune disorders with the pericentromeric region of chromosome 16 has led to the identification of SLC5A11 as a potential autoimmune modifier. The KIAA1576 gene product has been provisionally designated KIAA1576 pending further characterization.

Gen-ID: 3384