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IHC-P analysis of human pancreas using GTX89324 Prealbumin antibody, Internal. Antigen retrieval : citrate buffer pH 6 Dilution : 10microg/ml
IHC-P analysis of human pancreas using GTX89324 Prealbumin antibody, Internal. Antigen retrieval : citrate buffer pH 6 Dilution : 10microg/ml
IHC-P analysis of human pancreas using GTX89324 Prealbumin antibody, Internal. Antigen retrieval : citrate buffer pH 6 Dilution : 10microg/ml

Prealbumin antibody, Internal

GTX89324
GeneTex
ApplicationsELISA, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
Product group Antibodies
ReactivityHuman
TargetTTR
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Overview

  • Supplier
    GeneTex
  • Product Name
    Prealbumin antibody, Internal
  • Delivery Days Customer
    9
  • Application Supplier Note
    IHC-P: 10microg/ml. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    ELISA, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Concentration
    0.50 mg/ml
  • Conjugate
    Unconjugated
  • Gene ID7276
  • Target name
    TTR
  • Target description
    transthyretin
  • Target synonyms
    ATTR; CTS; CTS1; epididymis luminal protein 111; HEL111; HsT2651; PALB; prealbumin, amyloidosis type I; TBPA; thyroxine-binding prealbumin; transthyretin; TTN
  • Host
    Goat
  • Isotype
    IgG
  • Protein IDP02766
  • Protein Name
    Transthyretin
  • Scientific Description
    This gene encodes one of the three prealbumins, which include alpha-1-antitrypsin, transthyretin and orosomucoid. The encoded protein, transthyretin, is a homo-tetrameric carrier protein, which transports thyroid hormones in the plasma and cerebrospinal fluid. It is also involved in the transport of retinol (vitamin A) in the plasma by associating with retinol-binding protein. The protein may also be involved in other intracellular processes including proteolysis, nerve regeneration, autophagy and glucose homeostasis. Mutations in this gene are associated with amyloid deposition, predominantly affecting peripheral nerves or the heart, while a small percentage of the gene mutations are non-amyloidogenic. The mutations are implicated in the etiology of several diseases, including amyloidotic polyneuropathy, euthyroid hyperthyroxinaemia, amyloidotic vitreous opacities, cardiomyopathy, oculoleptomeningeal amyloidosis, meningocerebrovascular amyloidosis and carpal tunnel syndrome. [provided by RefSeq, Aug 2017]
  • Reactivity
    Human
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203