NPT2b rabbit pAb

NPT2b rabbit pAb

AO-06-ES3834-50

NPT2b rabbit pAb 50μL

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Antibody Product Overview

ELK.NoES3834
Product nameNPT2b rabbit pAb
ReactivityHuman;Rat
ApplicationsWB;ELISA
Other nameSLC34A2; Sodium-dependent phosphate transport protein 2B; Sodium-phosphate transport protein 2B; Na(+)-dependent phosphate cotransporter 2B; NaPi3b; Sodium/phosphate cotransporter 2B; Na(+)/Pi cotransporter 2B; NaPi-2b; Solute carrier family 34 member 2
Size50μL
Unit price ($)148
Human gene ID10568
Human Swiss-ProtO95436
SourceRabbit
IsotypeIgG
TargetNPT2b
Fields>>Parathyroid hormone synthesis, secretion and action;>>Mineral absorption
Gene nameSLC34A2
Protein nameSodium-dependent phosphate transport protein 2B
Human gene linkView Human Gene
Human Swiss linkView Human Swiss-Prot
Mouse gene ID
Mouse gene link
Mouse Swiss-ProtQ9DBP0
Mouse Swiss linkView Mouse Swiss-Prot
Rat gene ID
Rat gene link
Rat Swiss-ProtQ9JJ09
Rat Swiss linkView Rat Swiss-Prot
ImmunogenSynthesized peptide derived from NPT2b . at AA range: 630-710
SpecificityNPT2b Polyclonal Antibody detects endogenous levels of NPT2b protein.
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
ClonalityPolyclonal
DilutionWestern Blot: 1/500 - 1/2000. ELISA: 1/20000. Not yet tested in other applications.
PurificationThe antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Concentration1 mg/ml
Storage stability-20°C/1 year
Molecular Weight (Da)
Observed band (KD)75kD
BackgroundThe protein encoded by this gene is a pH-sensitive sodium-dependent phosphate transporter. Phosphate uptake is increased at lower pH. Defects in this gene are a cause of pulmonary alveolar microlithiasis. Three transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, May 2010],
Functiondisease:Defects in SLC34A2 are a cause of pulmonary alveolar microlithiasis [MIM:265100]. Pulmonary alveolar microlithiasis is a rare disease characterized by the deposition of calcium phosphate microliths throughout the lungs. Most patients are asymptomatic for several years or even for decades and generally, the diagnosis is incidental to clinical investigations unrelated to the disease. Cases with early onset or rapid progression are rare. A 'sandstorm-appearing' chest roentgenogram is a typical diagnostic finding. The onset of this potentially lethal disease varies from the neonatal period to old age and the disease follows a long-term, progressive course, resulting in a slow deterioration of lung functions. Pulmonary alveolar microlithiasis is a recessive monogenic disease with full penetrance.,function:May be involved in actively transporting phosphate into cells via Na(+) cotransp
Subcellular locationMembrane; Multi-pass membrane protein.
ExpressionHighly expressed in lung. Also detected in pancreas, kidney, small intestine, ovary, testis, prostate and mammary gland. In lung, it is found in alveolar type II cells but not in bronchiolar epithelium.

Additional Images

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Western Blot analysis of extracts from rat kidney, K562 cells, using NPT2b Polyclonal Antibody. Secondary antibody(catalog#:RS0002) was diluted at 1:20000
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: AO-06-ES3834-50
: 10 Items
Hurry! only 10 items left in stock.

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