Solute Carrier Family 25, Member 38 (SLC25A38) ELISA Kits

SLC25A38 is a member of the mitochondrial carrier family. Additionally we are shipping SLC25A38 Antibodies (21) and SLC25A38 Proteins (4) and many more products for this protein.

list all ELISA KIts Gene Name GeneID UniProt
Anti-Human SLC25A38 SLC25A38 54977 Q96DW6
Anti-Mouse SLC25A38 SLC25A38 208638 Q91XD8
Anti-Rat SLC25A38 SLC25A38 301067 Q499U1
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More ELISA Kits for SLC25A38 Interaction Partners

Human Solute Carrier Family 25, Member 38 (SLC25A38) interaction partners

  1. the biochemical and molecular characterization of yeast Hem25p and human SLC25A38, providing evidence that they are mitochondrial carriers for glycine. In particular, the hem25Delta mutant manifests a defect in the biosynthesis of delta-aminolevulinic acid and displays reduced levels of downstream heme and mitochondrial cytochromes.

  2. Given the tolerability of glycine and folate in humans, this study points to a potential novel treatment for SLC25A38 congenital sideroblastic anemia

  3. This study findings reveal a novel role for appoptosin in neurological disorders with tau neuropathology, linking caspase-3 (show CASP3 ELISA Kits)-mediated tau cleavage to synaptic dysfunction and behavioral/motor defects.

  4. Letter/Case Report: novel frameshift mutation in SLC25A38 causing congenital sideroblastic anaemia.

  5. Several missense mutations are found in SLC25A38 in a Chinese population with congenital sideroblastic anemia.

  6. Compares and contrasts all the known human SLC25A (show SLC25A25 ELISA Kits)* genes and includes functional information.

  7. Mutations in the SLC25A38 gene cause severe, non-syndromic, microcytic/hypochromic sideroblastic anemia in many populations.

  8. Twelve CSA (show ERCC8 ELISA Kits) probands had biallelic mutations in SLC25A38

SLC25A38 Antigen Profile

Antigen Summary

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.

Gene names and symbols associated with SLC25A38

  • solute carrier family 25, member 38 (SLC25A38) antibody
  • solute carrier family 25, member 38 (Slc25a38) antibody
  • solute carrier family 25, member 38 (slc25a38) antibody
  • AV019094 antibody
  • BC010801 antibody
  • RGD1311914 antibody

Protein level used designations for SLC25A38

solute carrier family 25, member 38 , solute carrier family 25 member 38

420717 Gallus gallus
54977 Homo sapiens
477028 Canis lupus familiaris
512325 Bos taurus
208638 Mus musculus
301067 Rattus norvegicus
100147784 Ovis aries
446494 Xenopus laevis
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