TNAP rabbit pAb

TNAP rabbit pAb

AO-06-ES5398-50

TNAP rabbit pAb 50μL

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Antibody Product Overview

ELK.NoES5398
Product nameTNAP rabbit pAb
ReactivityHuman;Mouse;Rat
ApplicationsWB;ELISA
Other nameALPL; Alkaline phosphatase; tissue-nonspecific isozyme; AP-TNAP; TNSALP; Alkaline phosphatase liver/bone/kidney isozyme
Size50μL
Unit price ($)148
Human gene ID249
Human Swiss-ProtP05186
SourceRabbit
IsotypeIgG
TargetTNAP
Fields>>Thiamine metabolism;>>Folate biosynthesis;>>Metabolic pathways;>>Biosynthesis of cofactors
Gene nameALPL
Protein nameAlkaline phosphatase tissue-nonspecific isozyme
Human gene linkView Human Gene
Human Swiss linkView Human Swiss-Prot
Mouse gene ID11647
Mouse gene linkView Mouse Gene
Mouse Swiss-ProtP09242
Mouse Swiss linkView Mouse Swiss-Prot
Rat gene ID25586
Rat gene linkView Rat Gene
Rat Swiss-ProtP08289
Rat Swiss linkView Rat Swiss-Prot
ImmunogenThe antiserum was produced against synthesized peptide derived from human ALPL. AA range:201-250
SpecificityTNAP Polyclonal Antibody detects endogenous levels of TNAP protein.
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
ClonalityPolyclonal
DilutionWestern Blot: 1/500 - 1/2000. ELISA: 1/40000. 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)70kD
BackgroundThis gene encodes a member of the alkaline phosphatase family of proteins. There are at least four distinct but related alkaline phosphatases: intestinal, placental, placental-like, and liver/bone/kidney (tissue non-specific). The first three are located together on chromosome 2, while the tissue non-specific form is located on chromosome 1. The product of this gene is a membrane bound glycosylated enzyme that is not expressed in any particular tissue and is, therefore, referred to as the tissue-nonspecific form of the enzyme. Alternative splicing results in multiple transcript variants, at least one of which encodes a preproprotein that is proteolytically processed to generate the mature enzyme. This enzyme may play a role in bone mineralization. Mutations in this gene have been linked to hypophosphatasia, a disorder that is characterized by hypercalcemia and skeletal defects. [prov
Functioncatalytic activity:A phosphate monoester + H(2)O = an alcohol + phosphate.,cofactor:Binds 1 magnesium ion.,cofactor:Binds 2 zinc ions.,disease:Defects in ALPL are a cause of hypophosphatasia adult type (hypophosphatasia) [MIM:146300].,disease:Defects in ALPL are a cause of hypophosphatasia childhood (hypophosphatasia) [MIM:241510].,disease:Defects in ALPL are a cause of hypophosphatasia infantile (hypophosphatasia) [MIM:241500]; an inherited metabolic bone disease characterized by defective skeletal mineralization. Four hypophosphatasia forms are distinguished, depending on the age of onset: perinatal, infantile, childhood and adult type. The perinatal form is the most severe and is almost always fatal. Patients with only premature loss of deciduous teeth, but with no bone disease are regarded as having odontohypophosphatasia (odonto).,function:This isozyme may play a role in skeletal mi
Subcellular locationCell membrane ; Lipid-anchor, GPI-anchor . Extracellular vesicle membrane ; Lipid-anchor, GPI-anchor . Mitochondrion membrane ; Lipid-anchor, GPI-anchor . Mitochondrion intermembrane space . Localizes to special class of extracellular vesicles, named matrix vesicles (MVs), which are released by osteogenic cells. Localizes to the mitochondria of thermogenic fat cells: tethered to mitochondrial membranes via a GPI-anchor and probably resides in the mitochondrion intermembrane space. .
ExpressionBrain,Cerebellum,Liver,Lymphoma,Osteosarcoma,Peripheral nerve,Semin

Additional Images

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Western blot analysis of the lysates from Jurkat cells using ALPL antibody.
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: AO-06-ES5398-50
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