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CACNA1G Antibody

CAT: 0013-GTR17923944-01Size: 50 μLDry Ice: NoHazardous: No
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CAT#:0013-GTR17923944-01Size:50 μL
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Description
CACNA1G Antibody
Product Name Alternative
CACNA1G antibody; KIAA1123Voltage-dependent T-type calcium channel subunit alpha-1G antibody; Cav3.1c antibody; NBR13 antibody; Voltage-gated calcium channel subunit alpha Cav3.1 antibody
UniProt
O43497
Reactivity
Human, Rat
Immunogen
Synthetic peptide of Human CACNA1G
Target
CACNA1G
Clonality
Polyclonal
Conjugation
Unconjugated
Field of Research
Neuroscience
Purification
Antigen Affinity Purified
Dilution
ELISA:1:1000-1:2000, IHC-P:1:15-1:50
Form
Liquid
Storage Conditions
Maintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles.
Notes
For research use only.
Tested Applications
ELISA, IHC
Host or Source
Rabbit
Preservative
-20°C, pH7.4 PBS, 0.05% NaN3, 40% Glycerol
Isotype
IgG

UniProtKB · O43497

Voltage-dependent T-type calcium channel subunit alpha-1G

CAC1G_HUMAN · Homo sapiens

View on UniProt ↗
Primary accession
O43497
Review status
UniProtKB reviewed (Swiss-Prot)
Gene
CACNA1G
Protein existence
1: Evidence at protein level
Organism
Homo sapiens (Human)
Taxonomy ID
9606
Alternative names
—
EC number
—
Processing
—
Secondary accessions
D6RA64, E7EPR0, O43498, O94770, Q19QY8, Q19QY9, Q19QZ0, Q19QZ1, Q19QZ2, Q19QZ3, Q19QZ4, Q19QZ5, Q19QZ6, Q19QZ7, Q19QZ8, Q19QZ9, Q19R00, Q19R01, Q19R02, Q19R03, Q19R04, Q19R05, Q19R06, Q19R07, Q19R08, Q19R09, Q19R10, Q19R11, Q19R12, Q19R13, Q19R15, Q19R16, Q19R17, Q19R18, Q2TAC4, Q9NYU4, Q9NYU5, Q9NYU6, Q9NYU7, Q9NYU8, Q9NYU9, Q9NYV0, Q9NYV1, Q9UHN9, Q9UHP0, Q9ULU6, Q9UNG7, Q9Y5T2, Q9Y5T3
Protein keywords

Technical term

3D-structureProteomics identificationReference proteome

Coding sequence diversity

Alternative splicing

Ligand

Calcium

Molecular function

Calcium channelIon channelVoltage-gated channel

Biological process

Calcium transportIon transportTransport

Cellular component

Cell membraneCytoplasmMembrane

Disease

Disease variantNeurodegenerationSpinocerebellar ataxia

PTM

GlycoproteinPhosphoprotein

Domain

RepeatTransmembraneTransmembrane helix

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