Home > Product > Antibody > Rabbit Anti-KCNK9 antibody
KCNK 9; KCNK-9; TASK3; Potassium channel subfamily K member 9; Acid-sensitive potassium channel protein TASK-3; TWIK-related acid-sensitive K(+) channel 3; Two pore potassium channel KT3.2; Short=Two pore K(+) channel KT3.2; KCNK9_HUMAN
Cat:
SL5933R
Species Reactivity:
Mouse,Rat,(predicted: Human,Chicken,Pig,Cow,Horse,Rabbit,Sheep,)
Immunogen:
KLH conjugated synthetic peptide derived from human KCNK9:21-120/374<Extracellular>
Format:
Liquid
Storage instructions:
Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.
Concentration:
1mg/ml
Clonality:
Polyclonal
Isotype:
IgG
Applications:
WB=1:500-2000ELISA=1:5000-10000IHC-P=1:100-500IHC-F=1:100-500ICC=1:100-500IF=1:100-500(Paraffin sections need to do antigen repair)not yet tested in other applications.optimal dilutions/concentrations should be determined by the end user.
Host:
Rabbit
Product Overview:
Sample: Cerebrum (Mouse) Lysate at 40 ugCerebrum (Rat) Lysate at 40 ugPrimary: Anti- KCNK9 (SL5933R) at 1/1000 dilutionSecondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilutionPredicted band size: 40 kDObserved band size: 48 kDSample: Adrenal gland (Mouse) Lysate at 40 ugPrimary: Anti- KCNK9 (SL5933R) at 1/1000 dilutionSecondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilutionPredicted band size: 40 kDObserved band size: 48 kD
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Unit:
Price: $
Product PDFs
Datasheet:


KCNK9 or TASK-3 (TWIK-related Acid sensitive K+ channel) is a member of the potassium channel family of proteins that contain two-pore domain and four transmembrane domains. These channels are characterized as leak K+ channels that are sensitive to changes in the extracellular pH. The physiological functions of TASK channels are largely unknown; it has been proposed that they may be involved in the regulation of breathing, aldosterone secretion and anesthetic-mediated neuronal activity. They were found to act in neurons' membrane potential and in resting K+ currents.

Function:
pH-dependent, voltage-insensitive, background potassium channel protein.

Subcellular Location:
Membrane; Multi-pass membrane protein

Tissue Specificity:
Mainly found in the cerebellum. Also found in adrenal gland, kidney and lung.

DISEASE:
Defects in KCNK9 are the cause of Birk-Barel mental retardation dysmorphism syndrome (BIBAS) [MIM:612292]. A syndrome characterized by mental retardation, hypotonia, hyperactivity, and facial dysmorphism.

Similarity:
Belongs to the two pore domain potassium channel (TC 1.A.1.8)

SWISS:
Q9NPC2

Gene ID:
51305

Database links:

Entrez Gene: 428382 Chicken

Entrez Gene: 51305 Human

Omim: 605874 Human

SwissProt: Q9NPC2 Human

Unigene: 493037 Human



Picture

Sample:
Cerebrum (Mouse) Lysate at 40 ug
Cerebrum (Rat) Lysate at 40 ug
Primary: Anti- KCNK9 (SL5933R) at 1/1000 dilution
Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution
Predicted band size: 40 kD
Observed band size: 48 kD
Sample:
Adrenal gland (Mouse) Lysate at 40 ug
Primary: Anti- KCNK9 (SL5933R) at 1/1000 dilution
Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution
Predicted band size: 40 kD
Observed band size: 48 kD
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