ATP-Binding Cassette Sub-Family D Member 3 (ABCD3) Antibody

Este producto es parte de ABCD - ATP Binding Cassette Transporter D
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416€ (200 µl)

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935106861
info@markelab.com
name
ATP-Binding Cassette Sub-Family D Member 3 (ABCD3) Antibody
category
Primary Antibodies
provider
Abbexa
reference
abx431541
tested applications
P-ELISA, IHC, FCM

Description

ABCD3 Antibody is a Goat Polyclonal antibody against ABCD3.

Documents del producto

Instrucciones
Data sheet
Descargar

Product specifications

Category
Primary Antibodies
Immunogen Target
ATP-Binding Cassette Sub-Family D Member 3 (ABCD3)
Host
Goat
Reactivity
Human
Recommended Dilution
P-ELISA: 1/16000. Optimal dilutions/concentrations should be determined by the end user.
Clonality
Polyclonal
Conjugation
Unconjugated
Isotype
IgG
Purification
Purified from goat serum by ammonium sulphate precipitation followed by antigen affinity chromatography using the immunizing peptide.
Size 1
200 µl
Form
Liquid
Tested Applications
P-ELISA, IHC, FCM
Buffer
Tris saline, pH 7.3, containing 0.02% sodium azide and 0.5% bovine serum albumin.
Availability
Shipped within 5-10 working days.
Storage
Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles.
Dry Ice
No
UniProt ID
P28288
Gene ID
5825
NCBI Accession
NP_002849.1, NM_002858
OMIM
170995
Alias
ABC43,CBAS5,PMP70
Background
Antibody anti-ABCD3
Status
RUO
Note
Concentration: 0.5 mg/ml - 

Descripción

ABCD3, also known as PMP70, is a critical peroxisomal transporter involved in the import of a broad range of substrates, including bile acid intermediates, branched-chain fatty acids, and very-long-chain fatty acids (VLCFAs). It facilitates the transport of these molecules into peroxisomes, where they undergo β-oxidation or other metabolic processes. ABCD3 is highly expressed in tissues such as the liver, kidneys, and adrenal glands, reflecting its role in maintaining lipid homeostasis and detoxification. Mutations or dysregulation of ABCD3 can result in impaired peroxisomal function, contributing to disorders such as Zellweger spectrum disorders, characterized by defects in peroxisomal metabolism. ABCD3’s role in lipid transport underscores its significance in metabolic and developmental processes.

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