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Solute Carrier Family 33 Member 1 Proteins (SLC33A1)

The protein encoded by SLC33A1 is required for the formation of O-acetylated (Ac) gangliosides. Additionally we are shipping SLC33A1 Antibodies (43) and SLC33A1 Kits (1) and many more products for this protein.

list all proteins Gene Name GeneID UniProt
SLC33A1 9197 O00400
SLC33A1 11416 Q99J27
Rat SLC33A1 SLC33A1 64018 Q6AYY8
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Top SLC33A1 Proteins at antibodies-online.com

Showing 3 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 2 μg Log in to see 9 Days
$333.33
Details

SLC33A1 Proteins by Origin and Source

Origin Expressed in Conjugate
Human ,
,
Mouse (Murine)

More Proteins for Solute Carrier Family 33 Member 1 (SLC33A1) Interaction Partners

Human Solute Carrier Family 33 Member 1 (SLC33A1) interaction partners

  1. SLC33A1 can negatively regulate BMP signaling.

  2. IRE1 (show ERN1 Proteins)/XBP1 (show XBP1 Proteins) controls the induction of autophagy/ERAD(II) during the unfolded protein response by activating the ER membrane transporter SLC33A1/AT-1

  3. Homozygosity mapping displayed a region of commonality among three families at chromosome 3q25. Deep sequencing and conventional sequencing disclosed homozygous or compound heterozygous mutations for all affected subjects in SLC33A1.

  4. translocates acetyl-CoA (show LPCAT2 Proteins) into the ER lumen and is essential for cell viability

  5. A missense mutation in SLC33A1 causes autosomal-dominant spastic paraplegia.

SLC33A1 Protein Profile

Protein Summary

The protein encoded by this gene is required for the formation of O-acetylated (Ac) gangliosides. The encoded protein is predicted to contain 6 to 10 transmembrane domains, and a leucine zipper motif in transmembrane domain III. Defects in this gene have been reported to cause spastic paraplegia autosomal dominant type 42 (SPG42) in one Chinese family, but not in similar patients of European descent. Two transcript variants encoding the same protein have been found for this gene.

Gene names and symbols associated with SLC33A1

  • solute carrier family 33 (acetyl-CoA transporter), member 1 (slc33a1)
  • solute carrier family 33 (acetyl-CoA transporter), member 1 (SLC33A1)
  • solute carrier family 33 (acetyl-CoA transporter), member 1 (Slc33a1)
  • Acatn protein
  • AI315656 protein
  • AI788741 protein
  • AT-1 protein
  • AT1 protein
  • CCHLND protein
  • D630022N01Rik protein
  • SPG42 protein
  • zgc:63693 protein

Protein level used designations for SLC33A1

acetyl-coenzyme A transporter 1 , acetyl-coenzyme A transporter , AT-1 , acetyl-CoA transporter 1 , solute carrier family 33 member 1

GENE ID SPECIES
394083 Danio rerio
425029 Gallus gallus
9197 Homo sapiens
485724 Canis lupus familiaris
517797 Bos taurus
11416 Mus musculus
64018 Rattus norvegicus
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