KCNJ11 antibody
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- Target See all KCNJ11 Antibodies
- KCNJ11 (Potassium Inwardly-Rectifying Channel, Subfamily J, Member 11 (KCNJ11))
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Reactivity
- Human, Mouse, Rat
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Host
- Rabbit
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Clonality
- Polyclonal
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Conjugate
- This KCNJ11 antibody is un-conjugated
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Application
- ELISA, Immunohistochemistry (IHC)
- Characteristics
- Polyclonal Antibody
- Purification
- Affinity purification
- Immunogen
- Recombinant protein of human KCNJ11
- Isotype
- IgG
- Top Product
- Discover our top product KCNJ11 Primary Antibody
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anti-Potassium Inwardly-Rectifying Channel, Subfamily J, Member 11 (KCNJ11) (AA 172-390) antibody
KCNJ11 Reactivity: Human WB, ELISA, IHC Host: Rabbit Polyclonal unconjugated
anti-Potassium Inwardly-Rectifying Channel, Subfamily J, Member 11 (KCNJ11) (pThr224) antibodyKCNJ11 Reactivity: Human WB, ELISA, IF Host: Rabbit Polyclonal unconjugated
anti-Potassium Inwardly-Rectifying Channel, Subfamily J, Member 11 (KCNJ11) (AA 1-30), (N-Term) antibodyKCNJ11 Reactivity: Human, Mouse WB, FACS Host: Rabbit Polyclonal RB21238 unconjugated
anti-Potassium Inwardly-Rectifying Channel, Subfamily J, Member 11 (KCNJ11) (Internal Region) antibodyVerified KCNJ11 Reactivity: Human WB, ELISA, IHC Host: Goat Polyclonal unconjugated
anti-Potassium Inwardly-Rectifying Channel, Subfamily J, Member 11 (KCNJ11) (AA 301-390) antibodyKCNJ11 Reactivity: Human WB, ELISA Host: Mouse Polyclonal unconjugated
anti-Potassium Inwardly-Rectifying Channel, Subfamily J, Member 11 (KCNJ11) (Center) antibodyKCNJ11 Reactivity: Human, Mouse, Rat, Rabbit, Cow, Pig WB, IHC, IF, IC Host: Rabbit Polyclonal unconjugated
anti-Potassium Inwardly-Rectifying Channel, Subfamily J, Member 11 (KCNJ11) (AA 190-239) antibodyKCNJ11 Reactivity: Human, Mouse WB, ELISA, IHC, IF Host: Rabbit Polyclonal unconjugated
anti-Potassium Inwardly-Rectifying Channel, Subfamily J, Member 11 (KCNJ11) (AA 372-385), (C-Term), (Intracellular) antibodyKCNJ11 Reactivity: Human, Mouse, Rat WB, IHC, IF Host: Guinea Pig Polyclonal unconjugated
anti-Potassium Inwardly-Rectifying Channel, Subfamily J, Member 11 (KCNJ11) (Ser688) antibodyKCNJ11 Reactivity: Human, Mouse, Rat WB, ELISA, IHC, IF Host: Rabbit Polyclonal unconjugated
anti-Potassium Inwardly-Rectifying Channel, Subfamily J, Member 11 (KCNJ11) (AA 171-390) antibodyKCNJ11 Reactivity: Human WB Host: Rabbit Polyclonal unconjugated
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- Application Notes
- IHC 1:50-1:200
- Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- 0.6 mg/mL
- Buffer
- PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
- 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
- KCNJ11 (Potassium Inwardly-Rectifying Channel, Subfamily J, Member 11 (KCNJ11))
- Alternative Name
- KCNJ11 (KCNJ11 Products)
- Synonyms
- kir6.2 antibody, Kir6.2 antibody, mBIR antibody, BIR antibody, HHF2 antibody, IKATP antibody, KIR6.2 antibody, PHHI antibody, TNDM3 antibody, potassium voltage-gated channel subfamily J member 11 antibody, potassium inwardly-rectifying channel, subfamily J, member 11 antibody, potassium inwardly rectifying channel, subfamily J, member 11 antibody, KCNJ11 antibody, kcnj11 antibody, Kcnj11 antibody
- Background
- Potassium channels are present in most mammalian cells, where they participate in a wide range of physiologic responses. The protein encoded by this gene is an integral membrane protein and inward-rectifier type potassium channel. The encoded protein, which has a greater tendency to allow potassium to flow into a cell rather than out of a cell, is controlled by G-proteins and is found associated with the sulfonylurea receptor SUR. Mutations in this gene are a cause of familial persistent hyperinsulinemic hypoglycemia of infancy (PHHI), an autosomal recessive disorder characterized by unregulated insulin secretion. Defects in this gene may also contribute to autosomal dominant non-insulin-dependent diabetes mellitus type II (NIDDM), transient neonatal diabetes mellitus type 3 (TNDM3), and permanent neonatal diabetes mellitus (PNDM). Multiple alternatively spliced transcript variants that encode different protein isoforms have been described for this gene.
- UniProt
- Q14654
- Pathways
- Negative Regulation of Hormone Secretion
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