PA551205

THEM5 Polyclonal Antibody, Invitrogen™

Manufacturer: Thermo Scientific

Select a Size

Pack Size SKU Availability Price
Each of 1 PA551205-Each-of-1 In Stock ₹ 46,502.50

PA551205 - Each of 1

₹ 46,502.50

In Stock

Quantity

1

Base Price: ₹ 46,502.50

GST (18%): ₹ 8,370.45

Total Price: ₹ 54,872.95

Antigen

THEM5

Classification

Polyclonal

Conjugate

Unconjugated

Gene

THEM5

Gene Alias

ACOT15; Acyl-CoA thioesterase THEM5; acyl-coenzyme A thioesterase 15; Acyl-coenzyme A thioesterase THEM5; THEM5; Thioesterase superfamily member 5

Host Species

Rabbit

Purification Method

Antigen affinity chromatography

Regulatory Status

RUO

Gene ID (Entrez)

284486

Content And Storage

-20°C

Form

Liquid

Applications

Immunohistochemistry (Paraffin)

Concentration

0.4 mg/mL

Formulation

PBS with 40% glycerol and 0.05% sodium azide; pH 7.4

Gene Accession No.

Q8N1Q8

Gene Symbols

THEM5

Immunogen

Full length fusion protein of human THEM5

Quantity

100 μL

Primary or Secondary

Primary

Target Species

Human

Product Type

Antibody

Isotype

IgG

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Description

  • The antibody detects endogenous levels of total THEM5 protein
  • THEM5 (thioesterase superfamily member 5) is a 247 amino acid protein that belongs to the thioesterase superfamily
  • The gene that encodes THEM5 contains nearly 8,000 bases and maps to human chromosome 1q21.3
  • Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome
  • There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1
  • Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A
  • When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs
  • The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration
  • The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis
  • Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1
  • Has acyl-CoA thioesterase activity towards long-chain (C16 and C18) fatty acyl-CoA substrates, with a preference for linoleyl-CoA and other unsaturated long-chain fatty acid-CoA esters
  • Plays an important role in mitochondrial fatty acid metabolism, and in remodeling of the mitochondrial lipid cardiolipin
  • Required for normal mitochondrial function.