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Anti-NKCC1/SLC12A2 Polyclonal Antibody

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Catalog No. TMAB-09494

Anti-NKCC1/SLC12A2 Polyclonal Antibody is a Rabbit antibody targeting NKCC1/SLC12A2. Anti-NKCC1/SLC12A2 Polyclonal Antibody can be used in FCM.

Anti-NKCC1/SLC12A2 Polyclonal Antibody

Anti-NKCC1/SLC12A2 Polyclonal Antibody

😃Good
Catalog No. TMAB-09494
Anti-NKCC1/SLC12A2 Polyclonal Antibody is a Rabbit antibody targeting NKCC1/SLC12A2. Anti-NKCC1/SLC12A2 Polyclonal Antibody can be used in FCM.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
50 μL$2227-10 days7-10 days
100 μL$3747-10 days7-10 days
200 μL$5297-10 days7-10 days
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Product Introduction

Bioactivity
Description
Anti-NKCC1/SLC12A2 Polyclonal Antibody is a Rabbit antibody targeting NKCC1/SLC12A2. Anti-NKCC1/SLC12A2 Polyclonal Antibody can be used in FCM.
Ig Type
IgG
Reactivity
Human (predicted:Mouse,Rat,Chicken,Dog,Pig,Cow,Chimpanzee)
Application
Recommended Dose
FCM: 3μg/Test
Antibody Type
Polyclonal
Host SpeciesRabbit
Subcellular LocalizationMembrane; Multi-pass membrane protein.
Tissue SpecificityExpressed in many tissues.
ConstructionPolyclonal Antibody
PurificationProtein A purified
AppearanceLiquid
Formulation0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
Concentration1mg/ml
Research BackgroundNa-K-Cl cotransporters (NKCC) are channel proteins that aid in the transcellular movement of chloride across both secretory and absorptive epithelia. NKCC1 is expressed in muscle cells, neurons, and red blood cells. In the basolateral membrane of secretory epithelia, NKCC1 mediates active chloride secretion. The gene encoding human NKCC1 maps to chromosome 5q23.3. In mice, disruption of the NKCC1 gene leads to deafness and impaired balance. NKCC2 is specifically expressed in the kidney where it mediates active reabsorption of sodium chloride in the thick ascending limb of the loop of Henle. NKCC2 is sensitive to the clinically important diuretics furosemide and bumetanide. The gene encoding human NKCC2 maps to chromosome 15q15-q21 and mutations in this gene lead to Bartter’s syndrome, an inherited hypokalaemic alkalosis. NCCT is a thiazide-sensitive Na-Cl cotransporter that is primarily expressed in the distal convoluted tubule of the kidney where it accounts for a significant fraction of net renal sodium reabsorption. The gene for human NCCT map to chromosome 16q13. Mutations in the gene encoding NCCT cause Gitelman’s syndrome, a subset of Bartter’s syndrome.
Antigen Details
Immunogen
KLH conjugated synthetic peptide: human NKCC1
Antigen Species
Human
Gene Name
SLC12A2
Gene ID
Protein Name
Solute carrier family 12 member 2
Uniprot ID
Function
Electrically silent transporter system. Mediates sodium and chloride reabsorption. Plays a vital role in the regulation of ionic balance and cell volume.
Chemical Properties
Molecular WeightTheoretical: 132 kDa.
Stability & Storage
Stability & StorageStore at 2°C-8°C for 1 month. Store at -20°C or -80°C for 12 months. Avoid repeated freeze-thaw cycles.
TransportShipping with blue ice.

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Tech Support

Please see Inhibitor Handling Instructions for more frequently ask questions. Topics include: how to prepare stock solutions, how to store products, and cautions on cell-based assays & animal experiments, etc
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