SLC25A38 Antibodies

AND SLC25A38 ELISA kits, SLC25A38 Proteins

Many biological assays use antibodies to detect SLC25A38, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with SLC25A38 in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop SLC25A38 antibodies...

We validate the specificity of these antibodies to SLC25A38 by testing them on tissues known to express SLC25A38 positively and negatively. Browse below to find the SLC25A38 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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SLC25A38 Infographic by Boster Bio

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SLC25A38 (NM_017875) Human Over-expression Lysate

Human

$628
Cat # LS054977
100 µg

SLC25A38 Overview

Facts about Mitochondrial glycine transporter.

SLC25A38 3D structure. Source: alphafold

Mitochondrial glycine transporter (SLC25A38)

Mitochondrial glycine transporter that imports glycine to the mitochondrial matrix. Plays an essential role in supplying glycine for the first enzymatic step in heme biosynthesis, the condensation of glycine with succinyl-CoA to produce 5-aminolevulinate (ALA) from the mitochondrial matrix.

Required during erythropoiesis. .

Gene Information

Human
Gene Name:	SLC25A38
Uniprot:	Q96DW6
Entrez:	54977

Family

Belongs to:

mitochondrial carrier (TC 2.A.29) family

Alternative Names

FLJ20551; FLJ22703; solute carrier family 25 member 38; solute carrier family 25, member 38

Molecular Weight

Mass (kDA):
33.566 kDA

Genomic Context


Human

Location:	3p22.1
Sequence:	3; NC_000003.12 (39383353..39397351)

Tissue Specificity

Preferentially expressed in erythroid cells.

Subcellular Localizations

Mitochondrion inner membrane; Multi-pass membrane protein.

Diseases

Anemia
Hereditary Sideroblastic Anemia
Sideroblastic Anemia
Nervousness
Iron Deficiency Anemia
Secondary Acquired Sideroblastic Anemia
Pearson's Syndrome
Iron Overload

Hematological Disease
De Novo Mutation

Pathways

Transport
Translation
Cell Proliferation
Localization

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/SLC25A38

References

PMID: 16949250 by Haitina T., et al. Fourteen novel human members of mitochondrial solute carrier family 25 (SLC25) widely expressed in the central nervous system.

PMID: 19412178 by Guernsey D.L., et al. Mutations in mitochondrial carrier family gene SLC25A38 cause nonsyndromic autosomal recessive congenital sideroblastic anemia.