Alkaline Phosphatase (ALPL) (NM_001177520) Human Tagged ORF Clone Lentiviral Particle
CAT#: RC230101L3V
- LentiORF®
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Lenti ORF particles, ALPL (Myc-DDK tagged) - Human alkaline phosphatase, liver/bone/kidney (ALPL), transcript variant 3, 200ul, >10^7 TU/mL
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CNY 8,930.00
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规格
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Specifications
Product Data | |
Product Name | Alkaline Phosphatase (ALPL) (NM_001177520) Human Tagged ORF Clone Lentiviral Particle |
Synonyms | AP-TNAP; APTNAP; HOPS; HPPA; HPPC; HPPI; HPPO; TNALP; TNAP; TNSALP |
Vector | pLenti-C-Myc-DDK-P2A-Puro |
ACCN | NM_001177520 |
ORF Size | 1341 bp |
Sequence Data |
The ORF insert of this clone is exactly the same as(RC230101).
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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_001177520.1, NP_001170991.1 |
RefSeq ORF | 1344 bp |
Locus ID | 249 |
Protein Families | Druggable Genome |
Protein Pathways | Folate biosynthesis, Metabolic pathways |
MW | 49.4 kDa |
Gene Summary | This gene encodes a member of the alkaline phosphatase family of proteins. There are at least four distinct but related alkaline phosphatases: intestinal, placental, placental-like, and liver/bone/kidney (tissue non-specific). The first three are located together on chromosome 2, while the tissue non-specific form is located on chromosome 1. The product of this gene is a membrane bound glycosylated enzyme that is not expressed in any particular tissue and is, therefore, referred to as the tissue-nonspecific form of the enzyme. Alternative splicing results in multiple transcript variants, at least one of which encodes a preproprotein that is proteolytically processed to generate the mature enzyme. This enzyme may play a role in bone mineralization. Mutations in this gene have been linked to hypophosphatasia, a disorder that is characterized by hypercalcemia and skeletal defects. [provided by RefSeq, Oct 2015] |
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