SYT14 rabbit pAb
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SYT14 rabbit pAb
Background :
Synaptotagmin 14 (SYT14) Homo sapiens This gene 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 this gene 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 this gene is located on the long arm of chromosome 4. [provided by RefSeq, Dec 2011]Description :
Synaptotagmin 14 (SYT14) Homo sapiens This gene 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 this gene 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 this gene is located on the long arm of chromosome 4. [provided by RefSeq, Dec 2011],UniProt :
Q8NB59Swiss Prot :
Q8NB59Reactivity :
Human; MouseImmunogen :
Synthesized peptide derived from part region of human proteinTarget :
SYT14Clonality :
PolyclonalSource :
RabbitApplications :
WB; ELISAConcentration :
1 mg/mlDilution :
WB 1:500-2000 ELISA 1:5000-20000Buffer :
-20°C/1 yearMolecular Weight :
61kDStorage Conditions :
-20°C/1 yearObserved Molecular Weight :
61kDFragment :
IgGSubcellular Location :
Membrane ; Single-pass type III membrane protein . Localized in perinuclear and submembranous regions.Gene ID (Human) :
255928
