ALPL 293T Cell Transient Overexpression Lysate(Denatured)

Catalog # H00000249-T01

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Size:100 uL
Price: USD $ 247.00
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Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
Images
SDS-PAGE Gel
QC Test

SDS-PAGE Gel

ALPL transfected lysate.

Western Blot
QC Test

Western Blot

Lane 1: ALPL transfected lysate ( 57.75 KDa)
Lane 2: Non-transfected lysate.

  • Specification

    Transfected Cell Line

    293T

    Plasmid

    pCMV-ALPL full-length

    Host

    Human

    Theoretical MW (kDa)

    57.75

    Interspecies Antigen Sequence

    Mouse (91)

    Quality Control Testing

    Transient overexpression cell lysate was tested with Anti-ALPL antibody (H00000249-B01) by Western Blots.

    SDS-PAGE Gel

    ALPL transfected lysate.

    Western Blot

    Lane 1: ALPL transfected lysate ( 57.75 KDa)
    Lane 2: Non-transfected lysate.

    Storage Buffer

    1X Sample Buffer (50 mM Tris-HCl, 2% SDS, 10% glycerol, 300 mM 2-mercaptoethanol, 0.01% Bromophenol blue)

    Storage Instruction

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

  • Applications

    Western Blot

  • Gene Info — ALPL

    Entrez GeneID

    249

    GeneBank Accession#

    ENST00000344573

    Protein Accession#

    -

    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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