CACNG3 (Human) Recombinant Protein (Q01)
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More Files
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Specification
Product Description
Human CACNG3 partial ORF ( NP_006530, 199 a.a. - 297 a.a.) recombinant protein with GST-tag at N-terminal.
Sequence
IYIEKHQQLRAKSHSEFLKKSTFARLPPYRYRFRRRSSSRSTEPRSRDLSPISKGFHTIPSTDISMFTLSRDPSKITMGTLLNSDRDHAFLQFHNSTPK
Host
Wheat Germ (in vitro)
Theoretical MW (kDa)
36.63
Preparation Method
Purification
Glutathione Sepharose 4 Fast Flow
Quality Control Testing
12.5% SDS-PAGE Stained with Coomassie Blue.
Storage Buffer
50 mM Tris-HCI, 10 mM reduced Glutathione, pH=8.0 in the elution buffer.
Storage Instruction
Store at -80°C. Aliquot to avoid repeated freezing and thawing.
Note
Best use within three months from the date of receipt of this protein.
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Applications
Enzyme-linked Immunoabsorbent Assay
Western Blot (Recombinant protein)
Antibody Production
Protein Array
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Gene Info — CACNG3
Entrez GeneID
10368GeneBank Accession#
NM_006539Protein Accession#
NP_006530Gene Name
CACNG3
Gene Alias
Cacng2
Gene Description
calcium channel, voltage-dependent, gamma subunit 3
Omim ID
606403Gene Ontology
HyperlinkGene Summary
L-type calcium channels are composed of five subunits. The protein encoded by this gene represents one of these subunits, gamma, and is one of several gamma subunit proteins. It is an integral membrane protein that is thought to stabilize the calcium channel in an inactive (closed) state. This protein is similar to the mouse stargazin protein, mutations in which have been associated with absence seizures, also known as petit-mal or spike-wave seizures. This gene is a member of the neuronal calcium channel gamma subunit gene subfamily of the PMP-22/EMP/MP20 family. This gene is a candidate gene for a familial infantile convulsive disorder with paroxysomal choreoathetosis. [provided by RefSeq
Other Designations
neuronal voltage-gated calcium channel gamma-3 subunit|voltage-dependent calcium channel gamma-3 subunit|voltage-gated calcium channel gamma subunit
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Interactome
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Disease
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