Acyl-CoA Thioesterase 7 (ACOT7) Antibody

Este producto es parte de ACOT - Acyl-CoA Thioesterase
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637€ (100 µl)

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935106861
info@markelab.com
name
Acyl-CoA Thioesterase 7 (ACOT7) Antibody
category
Primary Antibodies
provider
Abbexa
reference
abx110802
tested applications
ELISA, WB, IHC

Description

Acyl-Coa Thioesterase 7 Antibody is a Rabbit Polyclonal antibody against Acyl-Coa Thioesterase 7.

Documents del producto

Instrucciones
Data sheet
Descargar

Product specifications

Category
Primary Antibodies
Immunogen Target
Acyl-CoA Thioesterase 7 (ACOT7)
Host
Rabbit
Reactivity
Human, Mouse, Rat
Recommended Dilution
Optimal dilutions/concentrations should be determined by the end user.
Clonality
Polyclonal
Conjugation
Unconjugated
Isotype
IgG
Purification
Antigen Affinity Chromatography.
Size 1
100 µl
Form
Liquid
Tested Applications
ELISA, WB, IHC
Buffer
PBS, pH 7.3, containing 0.02% Sodium Azide and 50% Glycerol.
Availability
Shipped within 5-10 working days.
Storage
Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles.
Dry Ice
No
UniProt ID
O00154
Gene ID
11332
NCBI Accession
NP_009205.3, NM_007274.3, NP_863654.1, NM_181864.2
OMIM
602587
Alias
ACT,ACH1,BACH,LACH,LACH1,hBACH,CTE-II
Background
Antibody anti-ACOT7
Status
RUO

Descripción

ACOT7, also known as brain acyl-CoA hydrolase, is a cytosolic enzyme that hydrolyzes medium- and long-chain acyl-CoA esters, influencing lipid metabolism and cellular energy dynamics. It is highly expressed in the brain and testis, where it plays a role in modulating lipid signaling molecules, such as arachidonic acid and its derivatives, which are critical for neuronal function and inflammation. ACOT7 regulates the intracellular availability of free fatty acids and CoA, impacting processes like membrane synthesis, signaling, and energy production. In the nervous system, it is involved in neuroprotection and the regulation of synaptic function. Dysregulation of ACOT7 has been linked to neuroinflammatory disorders, such as multiple sclerosis, and metabolic diseases that involve disrupted fatty acid signaling. Its tissue-specific functions highlight its importance in maintaining both neuronal and systemic lipid homeostasis.

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