ATP Binding Cassette Subfamily G Member 4 (ABCG4) Antibody

Este producto es parte de ABCG - ATP Binding Cassette Subfamily G
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292.5€ (200 µl)

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935106861
info@markelab.com
name
ATP Binding Cassette Subfamily G Member 4 (ABCG4) Antibody
category
Primary Antibodies
provider
Abbexa
reference
abx431539
tested applications
P-ELISA

Description

ABCG4 Antibody is a Goat Polyclonal antibody against ABCG4.

Documents del producto

Instrucciones
Data sheet
Descargar

Product specifications

Category
Primary Antibodies
Immunogen Target
Target: ATP Binding Cassette Subfamily G Member 4 (ABCG4)
Immunogen: abx615620 - C-Terminus: C-YLVLRYRVKSER
Host
Goat
Assay Type
Concentration: 0.5 mg/ml
Recommended Dilution
P-ELISA: 1/8000. 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
64137, 192663, 300664
NCBI Accession
NP_071452.2
Alias
WHITE2
Background
Antibody anti-ABCG4
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

ABCG4 is a member of the ATP-binding cassette (ABC) transporter family, subfamily G, primarily expressed in the brain, macrophages, and hematopoietic stem cells. This protein plays a key role in cellular lipid homeostasis, particularly in cholesterol and phospholipid transport. It is involved in maintaining membrane lipid composition and may contribute to processes like neuroprotection and immune cell function. Dysfunction or aberrant regulation of ABCG4 is implicated in lipid-related disorders and neurological diseases. Understanding its precise role is critical for exploring its therapeutic potential in metabolic and neurodegenerative conditions.

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