CACNA1H polyclonal antibody
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Specification
Product Description
Rabbit polyclonal antibody raised against recombinant CACNA1H.
Immunogen
Recombinant protein corresponding to amino acids of human CACNA1H.
Sequence
EEVSHITSSACPWQPTAEPHGPEASPVAGGERDLRRLYSVDAQGFLDKPGRADEQWRPSAELGSGEPGEAKAWGPEAEPALGARRKKKMSP
Host
Rabbit
Reactivity
Human
Form
Liquid
Purification
Antigen affinity purification
Isotype
IgG
Recommend Usage
Immunohistochemistry (1:10-1:20)
The optimal working dilution should be determined by the end user.Storage Buffer
In PBS, pH 7.2 (40% glycerol, 0.02% sodium azide)
Storage Instruction
Store at 4°C. For long term storage store at -20°C.
Aliquot to avoid repeated freezing and thawing.Note
This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Applications
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
Immunohistochemical staining of human placenta with CACNA1H polyclonal antibody (Cat # PAB23513) shows strong cytoplasmic positivity in trophoblastic cells at 1:10-1:20 dilution. -
Gene Info — CACNA1H
Entrez GeneID
8912Protein Accession#
O95180Gene Name
CACNA1H
Gene Alias
CACNA1HB, Cav3.2, EIG6, FLJ90484
Gene Description
calcium channel, voltage-dependent, T type, alpha 1H subunit
Omim ID
607904Gene Ontology
HyperlinkGene Summary
This gene encodes a T-type member of the alpha-1 subunit family, a protein in the voltage-dependent calcium channel complex. Calcium channels mediate the influx of calcium ions into the cell upon membrane polarization and consist of a complex of alpha-1, alpha-2/delta, beta, and gamma subunits in a 1:1:1:1 ratio. The alpha-1 subunit has 24 transmembrane segments and forms the pore through which ions pass into the cell. There are multiple isoforms of each of the proteins in the complex, either encoded by different genes or the result of alternative splicing of transcripts. Alternate transcriptional splice variants, encoding different isoforms, have been characterized for the gene described here. Studies suggest certain mutations in this gene lead to childhood absence epilepsy (CAE). [provided by RefSeq
Other Designations
calcium channel, voltage-dependent, T type, alpha 1Hb subunit|calcium channel, voltage-dependent, alpha 1H subunit|low-voltage-activated calcium channel alpha1 3.2 subunit|low-voltage-activated calcium channel alpha13.2 subunit|voltage dependent t-type ca
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Interactome
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Disease
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