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SOX3 (NM_005634) Human Tagged ORF Clone Lentiviral Particle
CAT＃: RC210859L1V
- LentiORF®
-
Lenti ORF particles, SOX3 (Myc-DDK tagged) - Human SRY (sex determining region Y)-box 3 (SOX3), 200ul, >10^7 TU/mL
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CNY 8,930.00
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Specifications
| Product Data | |
| Product Name | SOX3 (NM_005634) Human Tagged ORF Clone Lentiviral Particle |
| Synonyms | GHDX; MRGH; PHP; PHPX; SOXB |
| Vector | pLenti-C-Myc-DDK |
| ACCN | NM_005634 |
| ORF Size | 1338 bp |
| Sequence Data |
The ORF insert of this clone is exactly the same as(RC210859).
|
| OTI Disclaimer | Due to the inherent nature of this plasmid, standard methods to replicate additional amounts of DNA in E. coli are highly likely to result in mutations and/or rearrangements. Therefore, OriGene does not guarantee the capability to replicate this plasmid DNA. Additional amounts of DNA can be purchased from OriGene with batch-specific, full-sequence verification at a reduced cost. Please contact our customer care team at custsupport@origene.com or by calling 301.340.3188 option 3 for pricing and delivery. 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_005634.2 |
| RefSeq Size | 2074 bp |
| RefSeq ORF | 1341 bp |
| Locus ID | 6658 |
| MW | 45 kDa |
| Gene Summary | This gene encodes a member of the SOX (SRY-related HMG-box) family of transcription factors involved in the regulation of embryonic development and in the determination of the cell fate. The encoded protein may act as a transcriptional regulator after forming a protein complex with other proteins. Mutations in this gene have been associated with X-linked cognitive disability with growth hormone deficiency. [provided by RefSeq, Jul 2008] |
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