SLC25A29 Antibodies

AND SLC25A29 ELISA kits, SLC25A29 Proteins

Many biological assays use antibodies to detect SLC25A29, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with SLC25A29 in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop SLC25A29 antibodies...

We validate the specificity of these antibodies to SLC25A29 by testing them on tissues known to express SLC25A29 positively and negatively. Browse below to find the SLC25A29 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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SLC25A29 Infographic by Boster Bio

All SLC25A29 Products

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SLC25A29 (NM_001039355) Human Over-expression Lysate

Human

$628
Cat # LS123096
100 µg

Anti-SLC25A29 Antibody Picoband®

Human

ELISA, WB

$370
Cat # A11796-1
100 μg/vial

SLC25A29 Overview

Facts about Mitochondrial basic amino acids transporter.

SLC25A29 3D structure. Source: alphafold

Mitochondrial basic amino acids transporter (SLC25A29)

Transports arginine, lysine, homoarginine, methylarginine and, to a much lesser extent, ornithine and histidine (PubMed:24652292). Can restore ornithine transport in cells lacking the primary mitochondrial ornithine transporter SLC25A15 (PubMed:19287344).

Doesn't transport carnitine nor acylcarnitines (PubMed:24652292). Functions by both counter- exchange and uniport mechanisms (PubMed:24652292).

Gene Information

Human
Gene Name:	SLC25A29
Uniprot:	Q8N8R3
Entrez:	123096

Family

Belongs to:

mitochondrial carrier (TC 2.A.29) family

Alternative Names

C14orf69; CACL; CACT-like; carnitine-acylcarnitine translocase like; chromosome 14 open reading frame 69; FLJ38975; mitochondrial carnitine/acylcarnitine carrier protein CACL; Solute carrier family 25 member 29; solute carrier family 25, member 29

Molecular Weight

Mass (kDA):
32.062 kDA

Genomic Context


Human

Location:	14q32.2
Sequence:	14; NC_000014.9 (100277986..100306536, complement)

Subcellular Localizations

Mitochondrion inner membrane; Multi-pass membrane protein.

Diseases

Hyperornithinemia-hyperammonemia-homocitrullinuria Syndrome
Endometrial Polyp
Citrullinemia
Hyperammonemia

Pathways

Transport
Urea Cycle
Ornithine Transport
Aerobic Respiration
Proteolysis
Muscle Contraction
Oxidative Phosphorylation

Rna Processing

PTMs

Phosphorylation

Oxidation

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/SLC25A29

References

PMID: 19287344 by Camacho J.A., et al. The human and mouse SLC25A29 mitochondrial transporters rescue the deficient ornithine metabolism in fibroblasts of patients with the hyperornithinemia-hyperammonemia-homocitrullinuria (HHH) syndrome.

PMID: 24652292 by Porcelli V., et al. The human gene SLC25A29, of solute carrier family 25, encodes a mitochondrial transporter of basic amino acids.