89-132-888

TTR, Goat, Polyclonal Antibody, Abnova™

Manufacturer: Abnova Corporation

Select a Size

Pack Size SKU Availability Price
Each of 1 89-132-888-Each-of-1 In Stock ₹ 70,399.00

89-132-888 - Each of 1

₹ 70,399.00

In Stock

Quantity

1

Base Price: ₹ 70,399.00

GST (18%): ₹ 12,671.82

Total Price: ₹ 83,070.82

Antigen

TTR

Classification

Polyclonal

Conjugate

Unconjugated

Dilution

ELISA (1:1000) The optimal working dilution should be determined by the end user.

Gene

TTR

Gene Symbols

TTR

Immunogen

A synthetic peptide corresponding to human TTR.

Quantity

100 μg

Primary or Secondary

Primary

Target Species

Human

Form

Liquid

Applications

ELISA

Concentration

0.5 mg/mL

Description

Goat polyclonal antibody raised against synthetic peptide of TTR.

Formulation

In Tris saline, pH 7.3 (0.5% BSA, 0.02% sodium azide)

Gene Alias

HsT2651/PALB/TBPA

Host Species

Goat

Purification Method

Antigen affinity purification

Regulatory Status

RUO

Gene ID (Entrez)

7276

Content And Storage

Store at -20°C.Aliquot to avoid repeated freezing and thawing.

Related Products

Img

Abnova Corporation

89-133-403

--

Img

Abnova Corporation

89-133-106

--

Img

Abnova Corporation

89-132-849

--

Img

Abnova Corporation

89-132-516

--

Img

Abnova Corporation

89-133-092

--

Img

Abnova Corporation

89-133-226

--

Img

Abnova Corporation

89-118-897

--

Img

Abnova Corporation

89-132-828

--

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 nonamyloidogenic
  • 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 Sequence: C-YKVEIDTKSYWK