SYT14 anticorps

N° du produit ABIN7231622

L’anticorps anti-SYT14 Polyclonal Lapin est utilisé pour la détection de SYT14 dans des échantillons de Humain et Souris. Il a été validé pour WB et ELISA.

Aperçu rapide pour SYT14 anticorps (ABIN7231622)

Antigène: SYT14 (Synaptotagmin XIV (SYT14))

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp SYT14 est non-conjugé

Application: Western Blotting (WB), ELISA

Détail du produit anti-SYT14 anticorps

Fonction: Rabbit Anti-SYT14 Polyclonal Antibody

Specificité: The antibody detects endogenous levels of SYT14 protein

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

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

Isotype: IgG

Information d'application

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

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

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

Agent conservateur: ProClin

Précaution d'utilisation: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: -20 °C

Stockage commentaire: 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.

Date de péremption: 12 months

Détails sur SYT14

Antigène: SYT14 (Synaptotagmin XIV (SYT14))

Autre désignation: SYT14

Sujet: 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.

Poids moléculaire: 61kD

ID gène: 255928

UniProt: Q8NB59