LI Cadherin (CDH17) (NM_004063) Human Tagged ORF Clone Lentiviral Particle
CAT#: RC211298L1V
- LentiORF®
Lenti ORF particles, CDH17 (Myc-DDK tagged) - Human cadherin 17, LI cadherin (liver-intestine) (CDH17), transcript variant 1, 200ul, >10^7 TU/mL
Lentiviral Particles: DDK w/ Puro mGFP mGFP w/ Puro
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USD 365.00
Specifications
Product Data | |
Type | Human Tagged ORF Clone Lentiviral Particle |
Tag | Myc-DDK |
Symbol | LI Cadherin |
Synonyms | CDH16; HPT-1; HPT1 |
Mammalian Cell Selection | None |
Vector | pLenti-C-Myc-DDK |
ACCN | NM_004063 |
ORF Size | 2496 bp |
Sequence Data |
The ORF insert of this clone is exactly the same as(RC211298).
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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_004063.2 |
RefSeq Size | 3697 bp |
RefSeq ORF | 2499 bp |
Locus ID | 1015 |
UniProt ID | Q12864 |
Cytogenetics | 8q22.1 |
Protein Families | Transmembrane |
MW | 92.15 kDa |
Gene Summary | This gene is a member of the cadherin superfamily, genes encoding calcium-dependent, membrane-associated glycoproteins. The encoded protein is cadherin-like, consisting of an extracellular region, containing 7 cadherin domains, and a transmembrane region but lacking the conserved cytoplasmic domain. The protein is a component of the gastrointestinal tract and pancreatic ducts, acting as an intestinal proton-dependent peptide transporter in the first step in oral absorption of many medically important peptide-based drugs. The protein may also play a role in the morphological organization of liver and intestine. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2009] |
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