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Alkaline Phosphatase (Tissue Non-Specific) antibody

GTX100817
GeneTex
ApplicationsWestern Blot, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
Product group Antibodies
TargetALPL
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Overview

  • Supplier
    GeneTex
  • Product Name
    Alkaline Phosphatase (Tissue Non-Specific) antibody
  • Delivery Days Customer
    9
  • Application Supplier Note
    WB: 1:500-1:3000. IHC-P: 1:100-1:1000. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    Western Blot, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Concentration
    1 mg/ml
  • Conjugate
    Unconjugated
  • Gene ID249
  • Target name
    ALPL
  • Target description
    alkaline phosphatase, biomineralization associated
  • Target synonyms
    AP-TNAP, APTNAP, HOPS, HPPA, HPPC, HPPI, HPPO, TNALP, TNAP, TNS-ALP, TNSALP, alkaline phosphatase, tissue-nonspecific isozyme, alkaline phosphatase liver/bone/kidney isozyme, alkaline phosphatase, liver/bone/kidney, liver/bone/kidney-type alkaline phosphatase, phosphoamidase, phosphocreatine phosphatase, tissue non-specific alkaline phosphatase, tissue-nonspecific ALP
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDP05186
  • Protein Name
    Alkaline phosphatase, tissue-nonspecific isozyme
  • Scientific Description
    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]
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203

References

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  • Kengelbach-Weigand A, Thielen C, Bäuerle T, et al. Personalized medicine for reconstruction of critical-size bone defects - a translational approach with customizable vascularized bone tissue. NPJ Regen Med. 2021,6(1):49. doi: 10.1038/s41536-021-00158-8
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  • Yen YT, Chien M, Wu PY, et al. PP2A in LepR+ mesenchymal stem cells contributes to embryonic and postnatal endochondral ossification through Runx2 dephosphorylation. Commun Biol. 2021,4(1):658. doi: 10.1038/s42003-021-02175-1
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  • Ou L, Wang H, Wu Z, et al. Effects of cadmium on osteoblast cell line: Exportin 1 accumulation, p-JNK activation, DNA damage and cell apoptosis. Ecotoxicol Environ Saf. 2021,208:111668. doi: 10.1016/j.ecoenv.2020.111668
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  • Matoug-Elwerfelli M, Nazzal H, Raif EM, et al. Ex-vivo recellularisation and stem cell differentiation of a decellularised rat dental pulp matrix. Sci Rep. 2020,10(1):21553. doi: 10.1038/s41598-020-78477-x
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  • Agustina H, Asyifa I, Aziz A, et al. The Role of Osteocalcin and Alkaline Phosphatase Immunohistochemistry in Osteosarcoma Diagnosis. Patholog Res Int. 2018,2018:6346409. doi: 10.1155/2018/6346409
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  • Wang JY, Chen WM, Wen CS, et al. Du-Huo-Ji-Sheng-Tang and its active component Ligusticum chuanxiong promote osteogenic differentiation and decrease the aging process of human mesenchymal stem cells. J Ethnopharmacol. 2017,198:64-72. doi: 10.1016/j.jep.2016.12.011
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  • Weigand A, Beier JP, Schmid R, et al. Bone Tissue Engineering Under Xenogeneic-Free Conditions in a Large Animal Model as a Basis for Early Clinical Applicability. Tissue Eng Part A. 2017,23(5-6):208-222. doi: 10.1089/ten.TEA.2016.0176
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  • Boos AM, Weigand A, Deschler G, et al. Autologous serum improves bone formation in a primary stable silica-embedded nanohydroxyapatite bone substitute in combination with mesenchymal stem cells and rhBMP-2 in the sheep model. Int J Nanomedicine. 2014,9:5317-39. doi: 10.2147/IJN.S66867
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  • Greenbaum AM, Revollo LD, Woloszynek JR, et al. N-cadherin in osteolineage cells is not required for maintenance of hematopoietic stem cells. Blood. 2012,120(2):295-302. doi: 10.1182/blood-2011-09-377457
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