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ELISA detection of Transthyretin using GTX100577 for capture at a concentration of 5 microg/mL and GTX89324 for detection at a concentration of 5 microg/mL. The HRP-conjugated anti-goat IgG antibody (GTX26741) was diluted at 1:20,000-1:200,000 and used to detect the primary antibody.
ELISA detection of Transthyretin using GTX100577 for capture at a concentration of 5 microg/mL and GTX89324 for detection at a concentration of 5 microg/mL. The HRP-conjugated anti-goat IgG antibody (GTX26741) was diluted at 1:20,000-1:200,000 and used to detect the primary antibody.
ELISA detection of Transthyretin using GTX100577 for capture at a concentration of 5 microg/mL and GTX89324 for detection at a concentration of 5 microg/mL. The HRP-conjugated anti-goat IgG antibody (GTX26741) was diluted at 1:20,000-1:200,000 and used to detect the primary antibody.

Prealbumin ELISA Pair - Prealbumin antibody Pair

Research Use Only
GTX500029
GeneTex
ApplicationsELISA
Product group Antibodies
ReactivityMouse
TargetTTR
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Overview

  • Supplier
    GeneTex
  • Product Name
    Prealbumin ELISA Pair - Prealbumin antibody Pair
  • Delivery Days Customer
    9
  • Applications
    ELISA
  • Certification
    Research Use Only
  • 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
  • Scientific Description
    This gene encodes transthyretin, one of the three prealbumins including alpha-1-antitrypsin, transthyretin and orosomucoid. Transthyretin is a carrier protein; it transports thyroid hormones in the plasma and cerebrospinal fluid, and also transports retinol (vitamin A) in the plasma. The protein consists of a tetramer of identical subunits. More than 80 different mutations in this gene have been reported; most mutations are related to amyloid deposition, affecting predominantly peripheral nerve and/or the heart, and a small portion of the gene mutations is non-amyloidogenic. The diseases caused by mutations include amyloidotic polyneuropathy, euthyroid hyperthyroxinaemia, amyloidotic vitreous opacities, cardiomyopathy, oculoleptomeningeal amyloidosis, meningocerebrovascular amyloidosis, carpal tunnel syndrome, etc. [provided by RefSeq]
  • Reactivity
    Mouse
  • Storage Instruction
    2°C to 8°C,-20°C or -80°C
  • UNSPSC
    12352203