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: SYT14 Polyclonal Antibody

Spezifität: The antibody detects endogenous levels of SYT14 protein

Aufreinigung: The antibody was affinity-purified from rabbit serum by affinity-chromatography using 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 (1:500-1:2000), ELISA (1:5000-1:20000).

Kommentare:

Primary Antibody

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 1 mg/mL

Buffer: PBS, pH 7.4, containing 0.02 % Sodium Azide as preservative and 50 % Glycerol.

Konservierungsmittel: Sodium azide

Vorsichtsmaßnahmen: This product contains Sodium azide: 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.

Details zu SYT14

Target: SYT14 (Synaptotagmin XIV (SYT14))

Andere Bezeichnung: SYT14

Hintergrund: Rabbit Anti-SYT14 Polyclonal Antibody,Synaptotagmin-14, Synaptotagmin XIV, SytXIV,SYT14 (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.,SYT14

Molekulargewicht: observerd band 61kDa

Gen-ID: 255928

UniProt: Q8NB59