DCC (NM_005215) Human Tagged ORF Clone Lentiviral Particle
CAT#: RC218506L2V
- LentiORF®
Lenti ORF particles, DCC (mGFP-tagged) - Human deleted in colorectal carcinoma (DCC), 200ul, >10^7 TU/mL
Lentiviral Particles: DDK DDK w/ Puro mGFP w/ Puro
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USD 365.00
Specifications
Product Data | |
Type | Human Tagged ORF Clone Lentiviral Particle |
Tag | mGFP |
Symbol | DCC |
Synonyms | CRC18; CRCR1; HGPPS2; IGDCC1; MRMV1; NTN1R1 |
Mammalian Cell Selection | None |
Vector | pLenti-C-mGFP |
ACCN | NM_005215 |
ORF Size | 4341 bp |
Sequence Data |
The ORF insert of this clone is exactly the same as(RC218506).
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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_005215.1 |
RefSeq Size | 4608 bp |
RefSeq ORF | 4344 bp |
Locus ID | 1630 |
UniProt ID | P43146 |
Cytogenetics | 18q21.2 |
Domains | ig, IGc2, IG, FN3 |
Protein Families | Druggable Genome, Transmembrane |
Protein Pathways | Axon guidance, Colorectal cancer, Pathways in cancer |
MW | 158.3 kDa |
Gene Summary | This gene encodes a netrin 1 receptor. The transmembrane protein is a member of the immunoglobulin superfamily of cell adhesion molecules, and mediates axon guidance of neuronal growth cones towards sources of netrin 1 ligand. The cytoplasmic tail interacts with the tyrosine kinases Src and focal adhesion kinase (FAK, also known as PTK2) to mediate axon attraction. The protein partially localizes to lipid rafts, and induces apoptosis in the absence of ligand. The protein functions as a tumor suppressor, and is frequently mutated or downregulated in colorectal cancer and esophageal carcinoma. [provided by RefSeq, Oct 2009] |
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