Phone:
+1 877 302 8632
Fax:
+1 888 205 9894 (Toll-free)
E-Mail:
orders@antibodies-online.com

TTHY antibody (N-Term)

This anti-TTHY antibody is a Rabbit Polyclonal antibody detecting TTHY in WB. Suitable for Human.
Catalog No. ABIN5514452

Quick Overview for TTHY antibody (N-Term) (ABIN5514452)

Target

TTHY (Thymocyte Alloantigen (TTHY))

Reactivity

Human

Host

Rabbit

Clonality

Polyclonal

Application

Western Blotting (WB)
  • Binding Specificity

    N-Term

    Sequence

    CPLMVKVLDA VRGSPAINVA VHVFRKAADD TWEPFASGKT SESGELHGLT

    Characteristics

    This is a rabbit polyclonal antibody against TTHY. It was validated on Western Blot.

    Purification

    Affinity purified

    Immunogen

    The immunogen is a synthetic peptide directed towards the N-terminal region of Human TTHY
  • Application Notes

    Optimal working dilution should be determined by the investigator.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.

    Preservative

    Sodium azide

    Precaution of Use

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Storage

    -20 °C

    Storage Comment

    For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
  • Target

    TTHY (Thymocyte Alloantigen (TTHY))

    Alternative Name

    TTHY

    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.

    Alias Symbols: TTR, PALB,

    Protein Size: 147

    Gene ID

    7276

    NCBI Accession

    NP_000362

    UniProt

    P02766
You are here:
Chat with us!