ATP Binding Cassette Subfamily G Member 4 (ABCG4) Antibody

Este producto es parte de ABCG - ATP Binding Cassette Subfamily G
ATP Binding Cassette Subfamily G Member 4 (ABCG4) Antibody
637€ (100 µl)

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Name
ATP Binding Cassette Subfamily G Member 4 (ABCG4) Antibody
Category
Primary Antibodies
Provider
Abbexa
Reference
abx111171
Tested Applications
ELISA, WB, IHC

Description

Atp-Binding Cassette, Sub-Family G (White), Member 4 Antibody is a Rabbit Polyclonal antibody against Atp-Binding Cassette, Sub-Family G (White), Member 4.

Documentos del producto

Instrucciones
Data sheet
Descargar

Especificaciones del producto

Category
Primary Antibodies
Immunogen Target
Target: ATP Binding Cassette Subfamily G Member 4 (ABCG4)
Immunogen: Human ABCG4.
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
Q9H172
Gene ID
64137
NCBI Accession
NP_001135977.1, NM_001142505.1
OMIM
607784
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.

Background

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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