KCNJ6 antibody
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- Target See all KCNJ6 Antibodies
- KCNJ6 (Potassium Inwardly-Rectifying Channel, Subfamily J, Member 6 (KCNJ6))
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Reactivity
- Human, Mouse
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Host
- Rabbit
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Clonality
- Polyclonal
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Conjugate
- This KCNJ6 antibody is un-conjugated
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Application
- Western Blotting (WB)
- Characteristics
- Polyclonal Antibody
- Purification
- Affinity purification
- Immunogen
- Recombinant fusion protein of human KCNJ6 (NP_002231.1).
- Isotype
- IgG
- Top Product
- Discover our top product KCNJ6 Primary Antibody
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- Application Notes
- WB 1:500-1:2000
- Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- 1 mg/mL
- Buffer
- PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
- Preservative
- Sodium azide
- Precaution of Use
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Storage
- -20 °C
- Storage Comment
- Store at -20°C. Avoid freeze / thaw cycles.
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- Target
- KCNJ6 (Potassium Inwardly-Rectifying Channel, Subfamily J, Member 6 (KCNJ6))
- Alternative Name
- KCNJ6 (KCNJ6 Products)
- Synonyms
- kcnj6 antibody, BIR1 antibody, GIRK-2 antibody, GIRK2 antibody, KATP-2 antibody, KATP2 antibody, KCNJ7 antibody, KIR3.2 antibody, hiGIRK2 antibody, Kir3.2 antibody, weaver antibody, wv antibody, potassium voltage-gated channel subfamily J member 6 antibody, potassium channel, inwardly rectifying subfamily J, member 5 antibody, potassium inwardly-rectifying channel, subfamily J, member 6 antibody, KCNJ6 antibody, kcnj5 antibody, Kcnj6 antibody
- Background
- This gene encodes a member of the G protein-coupled inwardly-rectifying potassium channel family of inward rectifier potassium channels. This type of potassium channel allows a greater flow of potassium into the cell than out of it. These proteins modulate many physiological processes, including heart rate in cardiac cells and circuit activity in neuronal cells, through G-protein coupled receptor stimulation. Mutations in this gene are associated with Keppen-Lubinsky Syndrome, a rare condition characterized by severe developmental delay, facial dysmorphism, and intellectual disability.
- Molecular Weight
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Observed_MW: 48 kDa
Calculated_MW: 48 kDa
- Gene ID
- 3763
- UniProt
- P48051
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