SYT14 Antikörper

Produktnummer ABIN7231622

Der Kaninchen Polyklonal anti-SYT14 Antikörper wird verwendet zum Nachweis von SYT14 in Proben von Human und Maus. Er wurde validiert für WB und ELISA.

Kurzübersicht für SYT14 Antikörper (ABIN7231622)

Target: SYT14 (Synaptotagmin XIV (SYT14))

Reaktivität: Human, Maus

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser SYT14 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), ELISA

Produktdetails anti-SYT14 Antikörper

Verwendungszweck: Rabbit Anti-SYT14 Polyclonal Antibody

Spezifität: The antibody detects endogenous levels of SYT14 protein

Aufreinigung: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Immunogen: Synthesized peptide derived from part region of human SYT14 protein

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB 1:500-2000,ELISA 1:5000-20000

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 1 mg/mL

Buffer: PBS, 50 % glycerol, 0.05 % Proclin 300, 0.05 %BSA

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: Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.

Haltbarkeit: 12 months

Details zu SYT14

Target: SYT14 (Synaptotagmin XIV (SYT14))

Andere Bezeichnung: SYT14

Hintergrund: Synaptotagmin-14, Synaptotagmin XIV, SytXIVSYT14 (Synaptotagmin 14) is a member of the synaptotagmin gene family and encodes a protein similar to other family members that mediate membrane trafficking in synaptic transmission. The encoded protein is a calcium-independent synaptotagmin. Mutations in SYT14 are a cause of autosomal recessive spinocerebellar ataxia-11 (SCAR11), and a t(1,3) translocation of this gene has been associated with neurodevelopmental abnormalities. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene, and a pseudogene of SYT14 is located on the long arm of chromosome 4.

Molekulargewicht: 61kD

Gen-ID: 255928

UniProt: Q8NB59