SYT14 anticorps

N° du produit ABIN7231622

L’anticorps Lapin Polyclonal anti-SYT14 a été validé pour WB et ELISA. Il convient pour détecter SYT14 dans des échantillons de Humain et Souris.

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: SYT14 Polyclonal Antibody

Specificité: The antibody detects endogenous levels of SYT14 protein

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

Commentaires:

Primary Antibody

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

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

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains Sodium azide: 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.

Détails sur SYT14

Antigène: SYT14 (Synaptotagmin XIV (SYT14))

Autre désignation: SYT14

Sujet: 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

Poids moléculaire: observerd band 61kDa

ID gène: 255928

UniProt: Q8NB59