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Solute Carrier Family 25, Member 38 Proteins (SLC25A38)

SLC25A38 is a member of the mitochondrial carrier family. Additionally we are shipping SLC25A38 Antibodies (20) and many more products for this protein.

list all proteins Gene Name GeneID UniProt
SLC25A38 54977 Q96DW6
SLC25A38 208638 Q91XD8
Rat SLC25A38 SLC25A38 301067 Q499U1
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Top SLC25A38 Proteins at antibodies-online.com

Showing 4 out of 4 products:

Catalog No. Origin Source Conjugate Images Quantity Supplier Delivery Price Details
Insect Cells Human rho-1D4 tag „Crystallography Grade“ protein due to multi-step, protein-specific purification process 0.5 mg Log in to see 49 to 54 Days
$6,041.49
Details
Insect Cells Mouse rho-1D4 tag „Crystallography Grade“ protein due to multi-step, protein-specific purification process 0.25 mg Log in to see 49 to 54 Days
$4,244.78
Details
HOST_Wheat germ Human GST tag 10 μg Log in to see 9 Days
$405.71
Details
HOST_Escherichia coli (E. coli) Human Un-conjugated   50 μg Log in to see 9 to 11 Days
$229.85
Details

SLC25A38 Proteins by Origin and Source

Origin Expressed in Conjugate
Human , ,
,
Mouse (Murine)

More Proteins for Solute Carrier Family 25, Member 38 (SLC25A38) Interaction Partners

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

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

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

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

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

  5. Compares and contrasts all the known human SLC25A (show SLC25A25 Proteins)* genes and includes functional information.

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

  7. Twelve CSA (show ERCC8 Proteins) probands had biallelic mutations in SLC25A38

SLC25A38 Protein Profile

Protein 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)
  • solute carrier family 25, member 38 (Slc25a38)
  • solute carrier family 25, member 38 (slc25a38)
  • AV019094 protein
  • BC010801 protein
  • RGD1311914 protein

Protein level used designations for SLC25A38

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

GENE ID SPECIES
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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