SLC33A1 antibody (clone 3A4), anti-human, rat
€435.00
In stock
SKU
AC-AT3921a
Catalog Number: AC-AT3921a
Size: 100 µg
Isotype: mouse IgG2a Kappa
Applications: WB, Ehttps://www.abcepta.com/products/pdf_download/AT3921a-SLC33A1-Antibody-monoclonal-M07">Request Information AC-AT3921a">Request Information
Size: 100 µg
Isotype: mouse IgG2a Kappa
Applications: WB, Ehttps://www.abcepta.com/products/pdf_download/AT3921a-SLC33A1-Antibody-monoclonal-M07">Request Information AC-AT3921a">Request Information
Background:
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.
Other Names:
Acetyl-coenzyme A transporter 1, AT-1, Acetyl-CoA transporter 1, Solute carrier family 33 member 1, SLC33A1, ACATN, AT1
Antigen Type:
Recombinant Protein
Gene Name: SLC33A1 (HGNC:95)
Gene ID: 9197
NCBI Accession: NP_001177921.1;NP_004724.1
Primary Accession: O00400
Other Accession: NM_004733
Format: Clear, colorless solution in phosphate buffered saline, pH 7.2 .
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.
Other Names:
Acetyl-coenzyme A transporter 1, AT-1, Acetyl-CoA transporter 1, Solute carrier family 33 member 1, SLC33A1, ACATN, AT1
Antigen Type:
Recombinant Protein
Gene Name: SLC33A1 (HGNC:95)
Gene ID: 9197
NCBI Accession: NP_001177921.1;NP_004724.1
Primary Accession: O00400
Other Accession: NM_004733
Format: Clear, colorless solution in phosphate buffered saline, pH 7.2 .
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