ATP Binding Cassette Subfamily G Member 4 (ABCG4) Antibody

292.5€ (200 µl)
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935106861
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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
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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