ABCD2 Antibodies

AND ABCD2 ELISA kits, ABCD2 Proteins

Many biological assays use antibodies to detect ABCD2, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with ABCD2 in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop ABCD2 antibodies...

We validate the specificity of these antibodies to ABCD2 by testing them on tissues known to express ABCD2 positively and negatively. Browse below to find the ABCD2 antibody that suites your experiment. We have 2 of these antibodies and many publications and validation images.

If you cannot find antibodies that fit your needs, contact us for making custom antibodies. We have a full suite of custom antibody services covering from research to diagnostic and therapeutic applications.

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ABCD2 Infographic by Boster Bio

All ABCD2 Products

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Product

Figures

Specificity

Applications

Price

Anti-ABCD2 Mouse Monoclonal Antibody [Clone ID: OTI3B7]

Human, Mouse, Rat

$523
Cat # M02566
100 µl

ABCD2 (NM_005164) Human Over-expression Lysate

Human

$628
Cat # LS000225
100 µg

ABCD2 Overview

Facts about ATP-binding cassette sub-family D member 2.

ABCD2 3D structure. Source: alphafold

ATP-binding cassette sub-family D member 2 (ABCD2)

Probable transporter. .

Gene Information

Human
Gene Name:	ABCD2
Uniprot:	Q9UBJ2
Entrez:	225

Family

Belongs to:

ABC transporter superfamily

Alternative Names

Adrenoleukodystrophy-like 1; Adrenoleukodystrophy-related protein; ALD1; ALDL1ATP-binding cassette sub-family D member 2; ALDRhALDR; ALDRPABC39; ATP-binding cassette, sub-family D (ALD), member 2

Molecular Weight

Mass (kDA):
83.233 kDA

Genomic Context


Human

Location:	12q12
Sequence:	12; NC_000012.12 (39530965..39651333, complement)

Tissue Specificity

Predominantly expressed in brain and heart.

Subcellular Localizations

Peroxisome membrane; Multi-pass membrane protein.

Diseases

Transient Ischemic Attack
Cerebrovascular Accident
Adrenoleukodystrophy
Stenosis
Atrial Fibrillation
Cardiac Fibrillation
Ischemic Stroke
Carotid Stenosis
Neurodegenerative Disorders
Peroxisomal Disorders
Diabetes Mellitus
Infarction

Demyelination
Hypertensive Disease
Nervousness
Weakness
Demyelinating Diseases
Brain Ischemia
Stricture Of Artery

Pathways

Transport
Pathogenesis
Fatty Acid Beta-oxidation
Localization
Brain Development
Inflammatory Response
Fatty Acid Transport
Cell Adhesion
Cell Proliferation
Sterol Transport
Fatty Acid Elongation
Aging
Spermatogenesis

Regulation Of Lipid Transport
Fatty Acid Homeostasis
Peroxisomal Transport
Histone Acetylation
Seed Germination
Cell Growth
Germination

PTMs

Oxidation
Farnesylation

Glycosylation
Acetylation

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/ABCD2

References

PMID: 8577752 by Lombard-Platet G., et al. A close relative of the adrenoleukodystrophy (ALD) gene codes for a peroxisomal protein with a specific expression pattern.

PMID: 9345306 by Holzinger A., et al. cDNA cloning and mRNA expression of the human adrenoleukodystrophy related protein (ALDRP), a peroxisomal ABC transporter.