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Kv10.2 rabbit pAb

CAT: 0855-ES20684-01Size: 50 µLDry Ice: NoHazardous: No
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CAT#:0855-ES20684-01Size:50 µL
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Background
This gene encodes a member of voltage-gated potassium channels. Members of this family have diverse functions, including regulating neurotransmitter and hormone release, cardiac function, and cell volume. This protein is an outward-rectifying, noninactivating channel. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]
Description
This gene encodes a member of voltage-gated potassium channels. Members of this family have diverse functions, including regulating neurotransmitter and hormone release, cardiac function, and cell volume. This protein is an outward-rectifying, noninactivating channel. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013],
UniProt
Q8NCM2
Swiss Prot
Q8NCM2
Reactivity
Human; Rat; Mouse
Immunogen
Synthetic Peptide of Kv10.2 AA range: 264-314
Clonality
Polyclonal
Source
Rabbit
Applications
WB; IHC; IF
Concentration
1 mg/ml
Dilution
WB 1:1000-2000, IHC 1:100-200
Molecular Weight
60kD
Storage Conditions
-20°C/1 year
Observed Molecular Weight
60kD
Fragment
IgG
Subcellular Location
Membrane; Multi-pass membrane protein.
Other Product Names
Potassium voltage-gated channel subfamily H member 5 (Ether-a-go-go potassium channel 2; hEAG2; Voltage-gated potassium channel subunit Kv10.2)
Gene ID (Human)
238271

UniProtKB · Q8NCM2

Voltage-gated delayed rectifier potassium channel KCNH5

KCNH5_HUMAN · Homo sapiens

View on UniProt ↗
Primary accession
Q8NCM2
Review status
UniProtKB reviewed (Swiss-Prot)
Gene
KCNH5
Protein existence
1: Evidence at protein level
Organism
Homo sapiens (Human)
Taxonomy ID
9606
Alternative names
—
EC number
—
Processing
—
Secondary accessions
C9JP98
Protein keywords

Technical term

3D-structureProteomics identificationReference proteome

Coding sequence diversity

Alternative splicing

Molecular function

Calmodulin-bindingIon channelPotassium channelVoltage-gated channel

Disease

Disease variantEpilepsyIntellectual disability

PTM

GlycoproteinIsopeptide bondPhosphoproteinUbl conjugation

Biological process

Ion transportPotassium transportTransport

Cellular component

Membrane

Ligand

Potassium

Domain

TransmembraneTransmembrane helix

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