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Rp1 (NM_001195662) Mouse Tagged ORF Clone Lentiviral Particle
CAT＃: MR226963L3V
- LentiORF®
-
Lenti ORF particles, Rp1 (Myc-DDK-tagged) - Mouse retinitis pigmentosa 1 (human) (Rp1), transcript variant 2, 200ul, >10^7 TU/mL
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CNY 7,410.00
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Specifications
| Product Data | |
| Product Name | Rp1 (NM_001195662) Mouse Tagged ORF Clone Lentiviral Particle |
| Synonyms | Dcdc3; Gm38717; mG145; O; Orp1; Rp; Rp1h |
| Vector | pLenti-C-Myc-DDK-P2A-Puro |
| ACCN | NM_001195662 |
| ORF Size | 855 bp |
| Sequence Data |
The ORF insert of this clone is exactly the same as(MR226963).
|
| 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_001195662.1, NP_001182591.1 |
| RefSeq Size | 3047 bp |
| RefSeq ORF | 858 bp |
| Locus ID | 19888 |
| Gene Summary | This gene encodes a member of the doublecortin family. The protein encoded by this gene contains two doublecortin domains, which bind microtubules and regulate microtubule polymerization. The encoded protein is a photoreceptor microtubule-associated protein and is required for correct stacking of outer segment disc. This protein and the RP1L1 protein, another retinal-specific protein, play essential and synergistic roles in affecting photosensitivity and outer segment morphogenesis of rod photoreceptors. Because of its response to in vivo retinal oxygen levels, this protein was initially named ORP1 (oxygen-regulated protein-1). This protein was subsequently designated RP1 (retinitis pigmentosa 1) when it was found that mutations in this gene cause autosomal dominant retinitis pigmentosa. Mutations in this gene also cause autosomal recessive retinitis pigmentosa. [provided by RefSeq, Jun 2019] |
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