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Alkaline Phosphatase, Tissue Non-Specific Antibody (V17.1), Novus Biologicals™

Mouse Monoclonal Antibody
Supplier: Novus Biologicals NBP2449620.2MG
Description
Ensure accurate, reproducible results in Flow Cytometry, Immunohistochemistry (Frozen), Immunofluorescence
Alkaline Phosphatase, Tissue Non-Specific Monoclonal antibody specifically detects Alkaline Phosphatase, Tissue Non-Specific in Human, Primate samples. It is validated for Flow Cytometry, Immunohistochemistry-Frozen, SDS-Page, Immunofluorescence.Specifications
Alkaline Phosphatase, Tissue Non-Specific | |
Monoclonal | |
0.2 mg/mL | |
Flow Cytometry 0.5 - 1 ug/million cells in 0.1 ml, Immunohistochemistry-Frozen 0.5 - 1.0 ug/ml, SDS-Page, Immunofluorescence 0.5 - 1.0 ug/ml | |
P05186, P05187 | |
ALPL | |
Bovine intestinal alkaline phosphatase | |
Protein A or G purified | |
RUO | |
249 | |
Human, Primate | |
Purified |
Flow Cytometry, Immunohistochemistry (Frozen), SDS-Page, Immunofluorescence | |
V17.1 | |
Unconjugated | |
10mM PBS and 0.05% BSA with 0.05% Sodium Azide | |
Alkaline phosphatase liver/bone/kidney isozyme, alkaline phosphatase, liver/bone/kidney, alkaline phosphatase, tissue-nonspecific isozyme, alkaline phosphomonoesterase, APTNAP, AP-TNAP, EC 3.1.3.1, FLJ40094, FLJ93059, glycerophosphatase, HOPS, liver/bone/kidney-type alkaline phosphatase, MGC161443, tissue-nonspecific ALP, TNAP, TNSALPMGC167935 | |
Mouse | |
55 kDa | |
0.2 mg | |
Primary | |
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. The exact physiological function of the alkaline phosphatases is not known. A proposed function of this form of the enzyme is matrix mineralization; however, mice that lack a functional form of this enzyme show normal skeletal development. This enzyme has been linked directly to hypo-phosphatasia, a disorder that is characterized by hypercalcemia and includes skeletal defects. The character of this disorder can vary, however, depending on the specific mutation since this determines age of onset and severity of symptoms. Alternatively spliced transcript variants, which encode the same protein, have been identified for this gene. | |
Store at 4C. | |
IgG1 κ |
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