RAI2 (NM_001172743) Human Untagged Clone
CAT＃: SC328874
RAI2 (untagged)-Human retinoic acid induced 2 (RAI2) transcript variant 1
CNY 7220.00
Product images
Specifications
| Product Data | |
| Type | Human Untagged Clone |
| Tag | Tag Free |
| Vector | pCMV6-XL5 |
| E. coli Selection | Ampicillin (100 ug/mL) |
| Mammalian Cell Selection | None |
| Sequence Data |
>NCBI ORF sequence for NM_001172743, the custom clone sequence may differ by one or more nucleotides
ATGGACGACCTGCAGTCCCAGAACCTCTCCATGGACATGACTGACTCCCCTCCTGCCTTG GCTAATAACAGACTGGAGAATGGCATGGCTCAGCTGATCACCACCGAGGCCTGGAACATC AACTCCACTGACCTGGTAAAGAAGGCCCTGGTGACCGTGCCAGCCCCATCCATTCTGAAC CCCCCTGCCGAGTCTCAGAGTGGCATGGCTCTGAAGGTGGCGGCCACTGTGTTGCAGCCC CTGTGCCTCGGGGAGAGCCCAGTGGTGATGCCCATTCACATGCAGGTGGAGGGAAGCTCC GCACCAGAGCTCAATCCGAATGGCAATGCCACCTACGTCATGACCACCCAGGGCCCCGTG CAACTGCCCGTGGTGCTGGAGCAGCACGTCTTTCAGCACCTCAACTCCCCTCTGGTCCTG CCGCAGGAGGCCCCATGCTCCTCCAGTACCATCCACAACAACCTCTTCCAGGGAGCGGAG GACCCCGAGGCCCAGCCCCAGCTCCTGGACCTGAGGATCCCCAGCCAGCCGCAGGAGCCC ACTTTGCCATTTGAAGCTGTGCTCCAGAATTTGTTTCCCTCCCAGGGCACTCTCGGGCCC CCACCCTGTCAGCCTCCTCCTGGCTATGCCCCTGTGCCCCCACAGCCTTTTAGCTCCCCC TTGTCCCCCCTGGTCCCACCAGCCACCCTCTTGGTGCCGTATCCTGTAATCGTCCCCTTG CCTGTGCCAGTCCCTATTCCCATCCCCATCCCGGTGCCTCAGAGTTCTGAATCCAAGTTC AGCTCCAGTTTCCCCAAGCCACCATCTTCCTTCGGCCTGCACCCCTTTAAAGGCACCCAG ACCCCTCTGGAAAAAGATGAACTGAAGCCCTTTGACATCCTCCAGCCTAAGGAGTACTTC CAGCTCAGCCGCCACACGGTCATTAAGATGGGAAGTGAGAACGAGGCCCTGGATCTCTCC ATGAAGTCAGTGCCCTGGCTCAAGGCTGGTGAAGTCAGTCCCCCAATCTTCCAGGAAGAT GCAGCCCTAGACCTGTCAGTGGCAGCCCACCGGAAATCCGAGCCTCCCCCTGAGACACTG TATGACAGTGGTGCATCAGTGGACAGCTCAGGTCACACAGTGATGGAGAAACTTCCCAGT GGCATGGAAATTTCTTTTGCCCCTGCCACGTCCCATGAGGCCCCAGCCATGATGGATAGT CACATCAGCAGCAGTGATGCTGCTACCGAGATGCTCAGCCAGCCCAACCACCCCAGCGGC GAAGTCAAGGCTGAAAATAACATTGAGATGGTGGGCGAGTCCCAGGCGGCCAAGGTCATT GTCTCTGTCGAAGATGCTGTGCCTACCATATTCTGTGGCAAGATCAAAGGCCTCTCAGGG GTGTCCACCAAAAACTTCTCCTTCAAAAGAGAAGACTCCGTGCTTCAGGGCTATGACATC AACAGCCAAGGGGAAGAGTCCATGGGAAATGCAGAGCCCCTTAGGAAACCCATCAAAAAC CGGAGCATAAAGTTAAAGAAAGTGAACTCCCAGGAAATACACATGCTCCCAATCAAAAAA CAACGGCTGGCCACCTTTTTTCCAAGAAAGTAA |
| Restriction Sites | Please inquire |
| ACCN | NM_001172743 |
| OTI Disclaimer | Our molecular clone sequence data has been matched to the reference identifier above as a point of reference. Note that the complete sequence of our molecular clones may differ from the sequence published for this corresponding reference, e.g., by representing an alternative RNA splicing form or single nucleotide polymorphism (SNP). |
| OTI Annotation | This TrueClone is provided through our Custom Cloning Process that includes sub-cloning into OriGene's pCMV6 vector and full sequencing to provide a non-variant match to the expected reference without frameshifts, and is delivered as lyophilized plasmid DNA. |
| Product Components | The ORF clone is ion-exchange column purified and shipped in a 2D barcoded Matrix tube containing 10ug of transfection-ready, dried plasmid DNA (reconstitute with 100 ul of water). |
| Reconstitution | 1. Centrifuge at 5,000xg for 5min. 2. Carefully open the tube and add 100ul of sterile water to dissolve the DNA. 3. Close the tube and incubate for 10 minutes at room temperature. 4. Briefly vortex the tube and then do a quick spin (less than 5000xg) to concentrate the liquid at the bottom. 5. Store the suspended plasmid at -20°C. The DNA is stable for at least one year from date of shipping when stored at -20°C. |
| Note | Plasmids are not sterile. For experiments where strict sterility is required, filtration with 0.22um filter is required. |
| Reference Data | |
| RefSeq | NM_001172743.1, NP_001166214.1 |
| RefSeq Size | 2426 bp |
| RefSeq ORF | 1593 bp |
| Locus ID | 10742 |
| UniProt ID | Q9Y5P3 |
| Gene Summary | Retinoic acid plays a critical role in development, cellular growth, and differentiation. The specific function of this retinoic acid-induced gene has not yet been determined but it may play a role in development. The chromosomal location of this gene designates it to be a candidate for diseases such as Nance-Horan syndrome, sensorineural deafness, non-specific X-linked cognitive disability, oral-facial-digital syndrome, and Fried syndrome. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Feb 2010] Transcript Variant: This variant (1) encodes the longer isoform. Variants 1, 2 and 3 encode the same isoform (1). |
Documents
| Product Manuals |
| FAQs |
| SDS |
Resources
Other Versions
| SKU | Description | Size | Price |
|---|---|---|---|
| RC230236 | RAI2 (Myc-DDK-tagged)-Human retinoic acid induced 2 (RAI2), transcript variant 1 |
CNY 3944.00 |
|
| RC230236L3 | Lenti-ORF clone of RAI2 (Myc-DDK-tagged)-Human retinoic acid induced 2 (RAI2), transcript variant 1 |
CNY 5890.00 |
|
| RC230236L4 | Lenti-ORF clone of RAI2 (mGFP-tagged)-Human retinoic acid induced 2 (RAI2), transcript variant 1 |
CNY 5890.00 |
|
| RG230236 | RAI2 (tGFP-tagged) - Human retinoic acid induced 2 (RAI2), transcript variant 1 |
CNY 4370.00 |
