IMPAD1 (NM_017813) Human Tagged ORF Clone Lentiviral Particle
CAT#: RC209799L4V
- LentiORF®
Lenti ORF particles, IMPAD1 (mGFP-tagged) - Human inositol monophosphatase domain containing 1 (IMPAD1), 200ul, >10^7 TU/mL
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Specifications
Product Data | |
Type | Human Tagged ORF Clone Lentiviral Particle |
Tag | mGFP |
Symbol | IMPAD1 |
Synonyms | GPAPP; IMP-3; IMP 3; IMPA3 |
Mammalian Cell Selection | Puromycin |
Vector | pLenti-C-mGFP-P2A-Puro |
ACCN | NM_017813 |
ORF Size | 1077 bp |
Sequence Data |
The ORF insert of this clone is exactly the same as(RC209799).
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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_017813.2, NP_060283.2 |
RefSeq Size | 2438 |
RefSeq ORF | 1080 |
Locus ID | 54928 |
Domains | inositol_P |
Protein Families | Transmembrane |
MW | 38.5 kDa |
Gene Summary | This gene encodes a member of the inositol monophosphatase family. The encoded protein is localized to the Golgi apparatus and catalyzes the hydrolysis of phosphoadenosine phosphate (PAP) to adenosine monophosphate (AMP). Mutations in this gene are a cause of GRAPP type chondrodysplasia with joint dislocations, and a pseudogene of this gene is located on the long arm of chromosome 1. [provided by RefSeq, Dec 2011] |
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