ALPL monoclonal antibody, clone V17.1

Catalog # MAB21196

Size

Price

Stock

Quantity

Size:100 ug
Price: USD $ 428.00
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Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
  • Specification

    Product Description

    Mouse monoclonal antibody raised against human ALPL.

    Immunogen

    Bovine intestinal alkaline phosphatase.

    Host

    Mouse

    Theoretical MW (kDa)

    55

    Reactivity

    Human

    Form

    Liquid

    Purification

    Protein A/G purification

    Isotype

    IgG1, kappa

    Recommend Usage

    Flow Cytometry (0.5-1 ug/106 cells)
    Immunofluorescence (0.5-1 ug/mL)
    Immunohistochemistry (Frozen sections) (0.5-1 ug/mL)
    The optimal working dilution should be determined by the end user.

    Storage Buffer

    In 10 mM PBS.

    Storage Instruction

    Store at -20 to -80°C.
    Aliquot to avoid repeated freezing and thawing.

  • Applications

    Immunohistochemistry (Frozen sections)

    Immunofluorescence

    Flow Cytometry

  • Gene Info — ALPL

    Entrez GeneID

    249

    Protein Accession#

    P05186

    Gene Name

    ALPL

    Gene Alias

    AP-TNAP, FLJ40094, FLJ93059, HOPS, MGC161443, MGC167935, TNAP, TNSALP

    Gene Description

    alkaline phosphatase, liver/bone/kidney

    Omim ID

    146300 171760 241500 241510

    Gene Ontology

    Hyperlink

    Gene Summary

    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, which encode the same protein, have been identified for this gene. [provided by RefSeq

    Other Designations

    OTTHUMP00000002971|OTTHUMP00000002972|alkaline phosphatase, tissue-nonspecific isozyme|alkaline phosphomonoesterase|glycerophosphatase|liver/bone/kidney-type alkaline phosphatase|tissue non-specific alkaline phosphatase|tissue-nonspecific ALP

  • Interactome
  • Pathway
  • Disease
Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
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