本公司产品仅供体外研究使用,不用于临床诊断

TTR Monoclonal Antibody

规格: / 20μL / 60μL / 120μL
价格: / ¥580 / ¥1420 / ¥2310

货号:E-AB-22255

宿主: Mouse

反应性: H

应用: WB,IHC-p

  • 详情
  • Overview

    Synonyms Amyloid polyneuropathy,Amyloidosis I,ATTR,Carpal tunnel syndrome 1,CTS,CTS1,Dysprealbuminemic euthyroidal hyperthyroxinemia,Dystransthyretinemic hyperthyroxinemia,Epididymis luminal protein 111,HEL111,HsT2651,PALB,Prealbumin amyloidosis type I,Prealbumin,Prealbumin Thyroxine-binding,Senile systemic amyloidosis,TBPA,Thyroxine binding prealbumin,Transthyretin,TTHY,TTR,TTR protein,TTR Mouse (3F2)抗体
    Swissprot P02766
    Source Mouse
    Reactivity Human
    Immunogen Recombinant Protein of TTR
    Application WB(Detection kit: E-IR-R304),IHC-p(Detection kit: E-IR-R213)
    Recommended dilution WB 1:500-2000, IHC 1:50-300
    Concentration 1mg/mL
    Clonality Monoclonal

    Properties

    Cellular localization Secreted. Cytoplasm.
    Tissue specificity Detected in serum and cerebrospinal fluid (at protein level). Highly expressed in choroid plexus epithelial cells. Detected in retina pigment epithelium and liver.
    Clone No Clone:3F2
    Isotype IgG
    Purification Protein A purification
    Storage instructions Store at -20℃. Avoid freeze / thaw cycles.
    Storage buffer PBS with 0.02% sodium azide and 50% glycerol pH 7.4.
    Background 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.
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