Tissue expression
Cell line expression
Protein structure

SLC25A38

Solute carrier family 25 member 38
FLJ20551 
This gene is a member of the mitochondrial carrier family. The encoded protein is required during erythropoiesis and is important for the biosynthesis of heme. Mutations in this gene are the cause of autosomal congenital sideroblastic anemia (anemia, sideroblastic, 2, pyridoxine-refractory). A related pseudogene is found on chromosome 1. [provided by RefSeq, Aug 2017]
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130 antibodies from 26 providers.

Antibody properties

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AntibodyRefsTypeWBELICCIPIHCFC
Invitrogen Antibodies
5 antibodies
Biorbyt
15 antibodies
St John's Laboratory
2 antibodies
antibodies-online
45 antibodies
Novus Biologicals
3 antibodies
OriGene
2 antibodies
Aviva Systems Biology
2 antibodies
GeneTex
1 antibody
Cusabio Biotech Co., Ltd
6 antibodies
ProSci
2 antibodies
NovoPro Bioscience Inc.
1 antibody
Bioss
3 antibodies
Abnova Corporation
2 antibodies
Atlas Antibodies
1 antibody
Creative Diagnostics
2 antibodies
RabMAbs
2 antibodies
Everest Biotech
1 antibody
Proteintech Group
1 antibody
Abbexa
6 antibodies
MyBioSource
3 antibodies
Abgent
2 antibodies
Leading Biology
2 antibodies
MilliporeSigma / Merck KGaA
1 antibody
GenWay
1 antibody
Creative Biolabs
2 antibodies