SYT14 antibody

Catalog No. ABIN7231622

The Rabbit Polyclonal anti-SYT14 antibody is suitable to detect SYT14 in samples from Human and Mouse. It has been validated for WB and ELISA.

Quick Overview for SYT14 antibody (ABIN7231622)

Target: SYT14 (Synaptotagmin XIV (SYT14))

Reactivity: Human, Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This SYT14 antibody is un-conjugated

Application: Western Blotting (WB), ELISA

Product Details anti-SYT14 Antibody

Purpose: SYT14 Polyclonal Antibody

Specificity: The antibody detects endogenous levels of SYT14 protein

Purification: 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

Isotype: IgG

Application Details

Application Notes: 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).

Comment:

Primary Antibody

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 mg/mL

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

Preservative: Sodium azide

Precaution of Use: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: -20 °C

Storage Comment: 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.

Target Details for SYT14

Target: SYT14 (Synaptotagmin XIV (SYT14))

Alternative Name: SYT14

Background: 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

Molecular Weight: observerd band 61kDa

Gene ID: 255928

UniProt: Q8NB59