Tissue expression
Cell line expression
Protein structure
SLC25A38
Solute carrier family 25 member 38FLJ20551
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]
Top validated antibodies |
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LSBio | LS-C40437 | Polyclonal |
WB
IHC |
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Biorbyt | orb452070 | Polyclonal |
WB
EL
ICC
IHC |
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Invitrogen Antibodies | PA5-42472 | 1 references | Polyclonal |
WB
IHC |
|
St John's Laboratory | STJ115184 | Polyclonal |
WB
ICC
IHC
|
||
antibodies-online | ABIN2030259 | Polyclonal |
WB
IHC |
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Supportive data in Antibodypedia
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Supportive data in Antibodypedia
Data presented on provider website
Data in Antibodypedia (inconclusive)
Recommended by provider