FEMA549884

Huntingtin Recombinant Rabbit Monoclonal Antibody (6F2), Invitrogen™

Manufacturer: Thermo Scientific

Select a Size

Pack Size SKU Availability Price
Each of 1 FEMA549884-Each-of-1 In Stock ₹ 37,202.00

FEMA549884 - Each of 1

₹ 37,202.00

In Stock

Quantity

1

Base Price: ₹ 37,202.00

GST (18%): ₹ 6,696.36

Total Price: ₹ 43,898.36

Antigen

Huntingtin

Classification

Recombinant Monoclonal

Concentration

0.63 mg/mL

Formulation

PBS with 50% glycerol and 0.02% sodium azide, pH 7.4

Gene Accession No.

P42858

Gene Symbols

Htt

Immunogen

A synthesized peptide derived from human Huntingtin

Quantity

100 μL

Primary or Secondary

Primary

Target Species

Human

Form

Liquid

Applications

ELISA, Immunohistochemistry (Paraffin)

Clone

6F2

Conjugate

Unconjugated

Gene

Htt

Gene Alias

AI256365, C430023I11Rik, Hd, HD protein, HD protein homolog, Hdh, HTT, Huntingtin, huntingtin (Huntington disease), Huntingtin, myristoylated N-terminal fragment, Huntington disease gene homolog, huntington disease protein, huntington disease protein homolog, IT15, solute carrier family 6 (neurotransmitter transporter, serotonin), member 4

Host Species

Rabbit

Purification Method

Affinity chromatography

Regulatory Status

RUO

Gene ID (Entrez)

3064

Content And Storage

-20°C or -80°C if preferred

Isotype

IgG

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Description

  • Huntingtin is a disease gene linked to Huntington's disease (HD), a neurodegenerative disorder characterized by loss of striatal neurons
  • This is thought to be caused by an expanded, unstable trinucleotide repeat in the huntingtin gene, which translates as a polyglutamine repeat in the protein product
  • HD is a mid-life onset autosomal dominant neurodegenerative disease that is characterized by psychiatric disorders, dementia, and involuntary movements (chorea), leading to death in 10-20 years.The huntingtin locus is large, spanning 180 kb and consisting of 67 exons
  • The huntingtin gene is widely expressed and is required for normal development
  • It is expressed as 2 alternatively polyadenylated forms displaying different relative abundance in various fetal and adult tissues
  • The larger transcript is approximately 13.7 kb and is expressed predominantly in adult and fetal brain whereas the smaller transcript of approximately 10.3 kb is more widely expressed
  • The genetic defect leading to Huntington's disease may not necessarily eliminate transcription, but may confer a new property on the mRNA or alter the function of the protein.