Use your antibodies-online credentials, if available.
No Products on your Comparison List.
Your basket is empty.
Find out more
The protein encoded by SLC33A1 is required for the formation of O-acetylated (Ac) gangliosides. Additionally we are shipping SLC33A1 Proteins (4) and many more products for this protein.
Showing 10 out of 44 products:
Human Monoclonal SLC33A1 Primary Antibody for RNAi, ELISA - ABIN563969
Jonas, Pehar, Puglielli: AT-1 is the ER membrane acetyl-CoA transporter and is essential for cell viability. in Journal of cell science 2010
Show all 2 references for ABIN563969
Human Polyclonal SLC33A1 Primary Antibody for WB - ABIN522651
Pehar, Jonas, Hare, Puglielli: SLC33A1/AT-1 protein regulates the induction of autophagy downstream of IRE1/XBP1 pathway. in The Journal of biological chemistry 2012
Show all 2 references for ABIN522651
Chicken Polyclonal SLC33A1 Primary Antibody for WB - ABIN2781611
Hirabayashi, Kanamori, Nomura, Nomura: The acetyl-CoA transporter family SLC33. in Pflügers Archiv : European journal of physiology 2004
SLC33A1 can negatively regulate BMP signaling.
IRE1 (show ERN1 Antibodies)/XBP1 (show XBP1 Antibodies) controls the induction of autophagy/ERAD(II) during the unfolded protein response by activating the ER membrane transporter SLC33A1/AT-1
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.
translocates acetyl-CoA (show LPCAT2 Antibodies) into the ER lumen and is essential for cell viability
A missense mutation in SLC33A1 causes autosomal-dominant spastic paraplegia.
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.
acetyl-coenzyme A transporter 1
, acetyl-coenzyme A transporter
, acetyl-CoA transporter 1
, solute carrier family 33 member 1