SLC33A1 (NM_004733) Human Tagged ORF Clone Lentiviral Particle

CAT#: RC204131L1V

  • LentiORF®

Lenti ORF particles, SLC33A1 (Myc-DDK tagged) - Human solute carrier family 33 (acetyl-CoA transporter), member 1 (SLC33A1), transcript variant 1, 200ul, >10^7 TU/mL

ORF Plasmid: DDK tGFP

Lentiviral Particles: DDK DDK w/ Puro mGFP mGFP w/ Puro

AAV Particle: DDK


Buy this product and get 50% off on the Lenti RapidTiter kit. Use Code: Rapid50

USD 1,061.00

2 Weeks*

Size
    • 200 ul

Product Images

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Specifications

Product Data
Type Human Tagged ORF Clone Lentiviral Particle
Tag Myc-DDK
Symbol SLC33A1
Synonyms ACATN; AT-1; AT1; CCHLND; SPG42
Mammalian Cell Selection None
Vector pLenti-C-Myc-DDK
ACCN NM_004733
ORF Size 1647 bp
Sequence Data
The ORF insert of this clone is exactly the same as(RC204131).
OTI Disclaimer The molecular sequence of this clone aligns with the gene accession number as a point of reference only. However, individual transcript sequences of the same gene can differ through naturally occurring variations (e.g. polymorphisms), each with its own valid existence. This clone is substantially in agreement with the reference, but a complete review of all prevailing variants is recommended prior to use. More info
OTI Annotation This clone was engineered to express the complete ORF with an expression tag. Expression varies depending on the nature of the gene.
Reference Data
RefSeq NM_004733.2
RefSeq Size 3811 bp
RefSeq ORF 1650 bp
Locus ID 9197
UniProt ID O00400
Cytogenetics 3q25.31
Protein Families Transmembrane
Protein Pathways Glycosphingolipid biosynthesis - ganglio series, Metabolic pathways
MW 60.9 kDa
Gene 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. [provided by RefSeq, Jul 2010]

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