KCNJ11 Polyclonal Antibody
Size: 200μL
Storage: Store at -20℃ Valid for 12 months. Avoid freeze / thaw cycles.
Shipping: The product is shipped with ice pack,upon receipt,store it immediately at the temperature recommended.
Exp date: 12 months
Category ID_II: Primary Antibodies
Category ID_III: Polyclonal Antibodies
Abbreviation: KCNJ11
Target Synonym: ATP sensitive inward rectifier potassium channel 11;Beta cell inward rectifier subunit;BIR;HHF 2;HHF2;IKATP;Inward rectifier K(+) channel Kir6.2;Inwardly rectifying potassium channel KIR6.2;IRK 11;IRK11;KCNJ11;Kir 6.2;Kir6.2;MGC133230;PHHI;Potassium channel inwardly rectifing subfamily J member 11;Potassium channel;inwardly rectifying subfamily J member 11;Potassium inwardly rectifying channel J11;TNDM 3;TNDM3
Research Areas: Cancer;Cardiovascular;Metabolism;Neuroscience;Signal Transduction
Conjugation: Unconjugated
Host: Rabbit
Species reactivity: Human;Mouse;Rat
Application: IHC
Isotype: IgG
Clonality: Polyclonal
Clone NO.:
UNIProt ID: Q14654
Accession:
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.
Concentration: 0.7 mg/mL
Immunogen: Recombinant protein of human KCNJ11
Buffer: PBS with 0.05% sodium azide and 50% glycerol, PH7.4
Purification method: Affinity purification
Dilution: IHC 1:50-1:200
Calculated MW:
ObservedMW:
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KCNJ11 Polyclonal Antibody
KCNJ11 Polyclonal Antibody
Size: 200μL
Storage: Store at -20℃ Valid for 12 months. Avoid freeze / thaw cycles.
Shipping: The product is shipped with ice pack,upon receipt,store it immediately at the temperature recommended.
Exp date: 12 months
Category ID_II: Primary Antibodies
Category ID_III: Polyclonal Antibodies
Abbreviation: KCNJ11
Target Synonym: ATP sensitive inward rectifier potassium channel 11;Beta cell inward rectifier subunit;BIR;HHF 2;HHF2;IKATP;Inward rectifier K(+) channel Kir6.2;Inwardly rectifying potassium channel KIR6.2;IRK 11;IRK11;KCNJ11;Kir 6.2;Kir6.2;MGC133230;PHHI;Potassium channel inwardly rectifing subfamily J member 11;Potassium channel;inwardly rectifying subfamily J member 11;Potassium inwardly rectifying channel J11;TNDM 3;TNDM3
Research Areas: Cancer;Cardiovascular;Metabolism;Neuroscience;Signal Transduction
Conjugation: Unconjugated
Host: Rabbit
Species reactivity: Human;Mouse;Rat
Application: IHC
Isotype: IgG
Clonality: Polyclonal
Clone NO.:
UNIProt ID: Q14654
Accession:
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.
Concentration: 0.7 mg/mL
Immunogen: Recombinant protein of human KCNJ11
Buffer: PBS with 0.05% sodium azide and 50% glycerol, PH7.4
Purification method: Affinity purification
Dilution: IHC 1:50-1:200
Calculated MW:
ObservedMW:
Product Information
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Shipping & Returns
Description
Size: 200μL
Storage: Store at -20℃ Valid for 12 months. Avoid freeze / thaw cycles.
Shipping: The product is shipped with ice pack,upon receipt,store it immediately at the temperature recommended.
Exp date: 12 months
Category ID_II: Primary Antibodies
Category ID_III: Polyclonal Antibodies
Abbreviation: KCNJ11
Target Synonym: ATP sensitive inward rectifier potassium channel 11;Beta cell inward rectifier subunit;BIR;HHF 2;HHF2;IKATP;Inward rectifier K(+) channel Kir6.2;Inwardly rectifying potassium channel KIR6.2;IRK 11;IRK11;KCNJ11;Kir 6.2;Kir6.2;MGC133230;PHHI;Potassium channel inwardly rectifing subfamily J member 11;Potassium channel;inwardly rectifying subfamily J member 11;Potassium inwardly rectifying channel J11;TNDM 3;TNDM3
Research Areas: Cancer;Cardiovascular;Metabolism;Neuroscience;Signal Transduction
Conjugation: Unconjugated
Host: Rabbit
Species reactivity: Human;Mouse;Rat
Application: IHC
Isotype: IgG
Clonality: Polyclonal
Clone NO.:
UNIProt ID: Q14654
Accession:
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.
Concentration: 0.7 mg/mL
Immunogen: Recombinant protein of human KCNJ11
Buffer: PBS with 0.05% sodium azide and 50% glycerol, PH7.4
Purification method: Affinity purification
Dilution: IHC 1:50-1:200
Calculated MW:
ObservedMW:
