SYT14 antibody
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.
Catalog No. ABIN7231622
$379.10
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Quick Overview for SYT14 antibody (ABIN7231622)
Target
See all SYT14 Antibodies
SYT14
(Synaptotagmin XIV (SYT14))
Reactivity
Human, Mouse
Host
Rabbit
Clonality
Polyclonal
Conjugate
This SYT14 antibody is un-conjugated
Application
Western Blotting (WB), ELISA
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Purpose
- Rabbit Anti-SYT14 Polyclonal Antibody
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Specificity
- The antibody detects endogenous levels of SYT14 protein
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Purification
- The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
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Immunogen
- Synthesized peptide derived from part region of human SYT14 protein
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Isotype
- IgG
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Application Notes
- Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB 1:500-2000,ELISA 1:5000-20000
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Restrictions
- For Research Use only
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Format
- Liquid
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Concentration
- 1 mg/mL
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Buffer
- PBS, 50 % glycerol, 0.05 % Proclin 300, 0.05 %BSA
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Preservative
- ProClin
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Precaution of Use
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Storage
- -20 °C
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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.
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Expiry Date
- 12 months
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- SYT14 (Synaptotagmin XIV (SYT14))
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Alternative Name
- SYT14
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Background
- 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.
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Molecular Weight
- 61kD
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Gene ID
- 255928
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UniProt
- Q8NB59
Target
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