SLC25A20 Antibodies

AND SLC25A20 ELISA kits, SLC25A20 Proteins

Many biological assays use antibodies to detect SLC25A20, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with SLC25A20 in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop SLC25A20 antibodies...

We validate the specificity of these antibodies to SLC25A20 by testing them on tissues known to express SLC25A20 positively and negatively. Browse below to find the SLC25A20 antibody that suites your experiment. We have 1 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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SLC25A20 Infographic by Boster Bio

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Anti-SLC25A20 Antibody

Human, Mouse, Rat

$405
Cat # A06410
100ul

SLC25A20 Overview

Facts about Mitochondrial carnitine/acylcarnitine carrier protein.

SLC25A20 3D structure. Source: alphafold

Mitochondrial carnitine/acylcarnitine carrier protein (SLC25A20)

Mediates the transport of acylcarnitines of different length across the mitochondrial inner membrane from the cytosol into the mitochondrial matrix for their oxidation by the mitochondrial fatty acid-oxidation pathway. .

Gene Information

Human
Gene Name:	SLC25A20
Uniprot:	O43772
Entrez:	788

Family

Belongs to:

mitochondrial carrier (TC 2.A.29) family

Alternative Names

CACCarnitine/acylcarnitine translocase; CACTSolute carrier family 25 member 20; mitochondrial carnitine/acylcarnitine carrier protein; solute carrier family 25 (carnitine/acylcarnitine translocase), member 20

Molecular Weight

Mass (kDA):
32.944 kDA

Genomic Context


Human

Location:	3p21.31
Sequence:	3; NC_000003.12 (48856926..48898882, complement)

Subcellular Localizations

Mitochondrion inner membrane; Multi-pass membrane protein.

Diseases

Cardiomyopathies
Hypoglycemia
Weakness
Muscle Weakness
Inborn Errors Of Metabolism
Hyperammonemia
Liver Dysfunction
Liver Failure
Encephalopathies
Cardiac Arrhythmia
Spinal Cord Injuries

Sudden Infant Death Syndrome
Inflammatory Response
Respiratory Distress
Cardiovascular Diseases
Cardiac Arrest
Pheochromocytoma

Pathways

Transport
Fatty Acid Oxidation
Neuroprotection
Fatty Acid Transport
Fatty Acid Beta-oxidation
Inflammatory Response

PTMs

Oxidation

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/SLC25A20

References

PMID: 9399886 by Huizing M., et al. Cloning of the human carnitine-acylcarnitine carrier cDNA and identification of the molecular defect in a patient.

PMID: 9837782 by Iacobazzi V., et al. The structure and organization of the human carnitine/acylcarnitine translocase (CACT) gene.