Polyclonal Antibodies
Anti-ABCD1 Rabbit Polyclonal Antibody for WB, IF/ICC, ELISA - P33897
Item Number : CM0013027
Price varies based on specs and customizations
- Application
- WB, IF/ICC, ELISA
- Cross Reactivity
- Human, Mouse
- Protein Weight
- 83kDa
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Core Product Specifications and Parameters
| Parameter | Value |
|---|---|
| Product Name | ABCD1 Rabbit pAb |
| Remarks/Alias | ALD; AMN; ALDP; ABC42; ABCD1 |
| Species | Human |
| Gene ID (Human) | 215 |
| Gene ID | 215 |
| Immunogen | Recombinant protein | Recombinant fusion protein containing a sequence corresponding to amino acids 340-500 of human ABCD1 (NP_000024.2). |
| Source | Rabbit |
| Category | Polyclonal Antibodies |
| Application | WB, IF/ICC, ELISA |
| Cross Reactivity | Human, Mouse |
| SWISS | P33897 |
| Protein Weight | 83kDa |
| Shipping | Ice bag |
Biological Background: ABCD1 Function and Localization
- ABCD1, also called adrenoleukodystrophy protein (ALDP), is a member of the ATP-binding cassette (ABC) transporter sub-family D, encoded by the ABCD1 (ALD) gene.
- It functions as an ATP-dependent transporter that imports very long chain fatty acyl-CoA (VLCFA-CoA) into peroxisomes, and also possesses fatty acyl-CoA thioesterase (ACOT) activity that hydrolyzes VLCFA-CoA prior to transport, an essential step in the import process. Related references: PMID:11248239, PMID:15682271, PMID:16946495, PMID:29397936, PMID:33500543
- Plays a central role in the degradation and biosynthesis of VLCFAs by regulating peroxisomal beta-oxidation, mitochondrial function, and microsomal fatty acid elongation. Related references: PMID:21145416, PMID:23671276
- Involved in myelination: negatively regulates microsomal fatty acid elongation during active myelination, and is required for axon and myelin maintenance.
- Controls the cellular response to oxidative stress by regulating mitochondrial oxidative phosphorylation and depolarization.
- Modulates the inflammatory response through positive regulation of peroxisomal VLCFA beta-oxidation.
- Subcellular localization includes peroxisomal, mitochondrial, lysosomal, and endoplasmic reticulum membranes, reflecting its multifaceted intracellular transport roles.
- Mutations in ABCD1 cause X-linked adrenoleukodystrophy (ALD), a severe neurodegenerative disorder marked by VLCFA accumulation.
Experimental Guidance and Technical Tips
- The immunogen corresponds to the C-terminal region (amino acids 340–500) of human ABCD1; validate detection of full-length protein and potential isoforms using appropriate positive controls.
- For Western blot, anticipate a specific band around 83 kDa; use human or mouse cell lines known to express ABCD1 (e.g., fibroblasts, brain tissue) to confirm reactivity.
- For immunofluorescence/ICC, optimize fixation/permeabilization conditions, and consider co-staining with peroxisomal markers to verify subcellular localization.
- ELISA-based detection should employ a recombinant ABCD1 protein standard matching the immunogen sequence for accurate quantification.
CamelBio: Your One-Stop Sourcing Bridge
CamelBio streamlines the procurement of IVD raw materials by offering a comprehensive portfolio of antibodies, antigens, and ancillary reagents. This ABCD1 polyclonal antibody supports research into peroxisomal disorders and VLCFA metabolism, and CamelBio can provide bulk-scale production, validated antibody pairs, and customized sourcing solutions to meet your diagnostic development needs. Partner with us to secure reliable raw materials and accelerate your assay pipeline.
Product Datasheet
Anti-ABCD1 Rabbit Polyclonal Antibody for WB, IF/ICC, ELISA - P33897
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