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E-AB-70384

ALPL Polyclonal Antibody

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£178.20

War £198.00

SKU:
E-AB-70384
Zusätzliche Namen:
AKP2,AP TNAP,AP-TNAP,APTNAP,Alkaline phosphatase,Alkaline phosphatase liver/bone/kidney,Alkaline phosphatase liver/bone/kidney isozyme,Alkaline phosphatase tissue nonspecific isozyme,Alkaline phosphomonoesterase,Alpl,BAP,FLJ4009,tissue-nonspecific isozyme
Anwendung:
WB
Konzentration:
200 ug/ml
Aufreinigung:
Affinity Purified
Lagerbedingungen:
-20[o]C Avoid freeze/thaw cycles.
Hersteller:
Elabscience
Host:
Rabbit
Reaktivitäten:
Human, Mouse, Rat
Buffer:
Phosphate buffered solution, pH 7.4, containing 0.05% stabilizer, 1% protein protectant and 50% glycerol.
Immunogen:
Recombinant protein corresponding to Mouse Alkaline Phosphatase
Uniprot:
P05186, P08289, P09242
Synonyme:
Ak;Akp;Akp-2;Akp2;Alkaline phosphatase 2;alkaline phosphatase 2, liver;alkaline phosphatase liver/bone/kidney isozyme;alkaline phosphatase, liver/bone/kidney;alkaline phosphatase, tissue-nonspecific isozyme;ALP;AP-TNAP;APTNAP;HOPS;HPPA;HPPC;HPPI;HPPO;liver/bone/kidney-type alkaline phosphatase;PHOA;T;tissue non-specific alkaline phosphatase;tissue-nonspecific alkaline phosphatase;tissue-nonspecific ALP;Tissue-nonspecific ALP alkaline phosphatase;TNALP;TNAP;TNSALP
Weitere Details:
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 hypophosphatasia, 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 have been described.
Versandbedingungen:
Blue Ice