ATP Binding Cassette Subfamily A Member 8 (ABCA8) Antibody

Este producto es parte de ABCA8 - ATP Binding Cassette Transporter A8
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292.5€ (200 µl)

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935106861
info@markelab.com
name
ATP Binding Cassette Subfamily A Member 8 (ABCA8) Antibody
category
Primary Antibodies
provider
Abbexa
reference
abx432260
tested applications
P-ELISA

Description

ABCA8 Antibody is a Goat Polyclonal antibody against ABCA8.

Documents del producto

Instrucciones
Data sheet
Descargar

Product specifications

Category
Primary Antibodies
Immunogen Target
Target: ATP Binding Cassette Subfamily A Member 8 (ABCA8)
Immunogen: abx615572 - C-Terminus: C-KEQELGDFEEDFD
Host
Goat
Assay Type
Concentration: 0.5 mg/ml
Recommended Dilution
P-ELISA: 1/4000. 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
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
Gene ID
10351
NCBI Accession
NP_009099.1
Alias
KIAA0822
Background
Antibody anti-ABCA8
Status
RUO
Note
THIS PRODUCT IS FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC, THERAPEUTIC OR COSMETIC PROCEDURES. NOT FOR HUMAN OR ANIMAL CONSUMPTION.

Descripción

ABCA8 is a member of the ATP-binding cassette transporter family, primarily involved in lipid transport and xenobiotic metabolism. It is highly expressed in the brain, liver, and kidneys, suggesting roles in lipid homeostasis and the clearance of toxins or drugs. ABCA8 is thought to facilitate the transport of cholesterol and sphingolipids across cellular membranes, contributing to cellular lipid regulation. In the brain, ABCA8 has been implicated in myelin formation and neuronal maintenance, where dysregulation may contribute to neurodegenerative diseases. Mutations or altered expression of ABCA8 have been associated with conditions such as multiple sclerosis and certain cancers. Its role in lipid metabolism and potential involvement in drug resistance highlight its importance in both physiological and pathological processes.

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