GLI2 (NM_005270) Human Tagged ORF Clone Lentiviral Particle
CAT#: RC217291L3V
- LentiORF®
Lenti ORF particles, GLI2 (Myc-DDK tagged) - Human GLI family zinc finger 2 (GLI2), 200ul, >10^7 TU/mL
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Specifications
Product Data | |
Product Name | GLI2 (NM_005270) Human Tagged ORF Clone Lentiviral Particle |
Synonyms | CJS; HPE9; PHS2; THP1; THP2 |
Vector | pLenti-C-Myc-DDK-P2A-Puro |
ACCN | NM_005270 |
ORF Size | 4758 bp |
Sequence Data |
The ORF insert of this clone is exactly the same as(RC217291).
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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_005270.3 |
RefSeq Size | 6549 bp |
RefSeq ORF | 4761 bp |
Locus ID | 2736 |
Protein Families | Adult stem cells, Cancer stem cells, Druggable Genome, Embryonic stem cells, ES Cell Differentiation/IPS |
Protein Pathways | Basal cell carcinoma, Hedgehog signaling pathway, Pathways in cancer |
MW | 167.6 kDa |
Gene Summary | This gene encodes a protein which belongs to the C2H2-type zinc finger protein subclass of the Gli family. Members of this subclass are characterized as transcription factors which bind DNA through zinc finger motifs. These motifs contain conserved H-C links. Gli family zinc finger proteins are mediators of Sonic hedgehog (Shh) signaling and they are implicated as potent oncogenes in the embryonal carcinoma cell. The protein encoded by this gene localizes to the cytoplasm and activates patched Drosophila homolog (PTCH) gene expression. It is also thought to play a role during embryogenesis. The encoded protein is associated with several phenotypes- Greig cephalopolysyndactyly syndrome, Pallister-Hall syndrome, preaxial polydactyly type IV, postaxial polydactyly types A1 and B. [provided by RefSeq, Jul 2008] |
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