SMCR7 (MIEF2) (NM_148886) Human Untagged Clone
CAT＃: SC306322
SMCR7 (untagged)-Human Smith-Magenis syndrome chromosome region, candidate 7 (SMCR7), transcript variant 2
CNY 7220.00
Product images
Specifications
| Product Data | |
| Type | Human Untagged Clone |
| Tag | Tag Free |
| Synonyms | COXPD49; MID49; SMCR7 |
| Vector | pCMV6 series |
| Sequence Data |
>NCBI ORF sequence for NM_148886, the custom clone sequence may differ by one or more nucleotides
ATGGGGCTGAGTCCCAATTTAGACAGGCAGACCATGGCAGAGTTCTCCCAGAAACGGGGG AAGCGGCGTAGCGACGAAGGGCTGGGCAGCATGGTGGACTTCCTCCTGGCCAATGCCCGC CTGGTGCTGGGCGTGGGCGGGGCTGCTGTGCTGGGCATTGCCACCCTGGCCGTGAAGCGG TTCATTGACAGGGCCACTAGCCCGCGGGATGAGGATGACACCAAGGCAGACAGCTGGAAG GAACTGAGCCTGCTCAAGGCCACACCACACCTGCAGCCCCGGCCTCCACCTGCTGCCCTT AGCCAGCCAGTGTTGCCCTTGGCCCCCTCGTCGTCTGCCCCAGAAGGGCCTGCAGAAACT GATCCTGAGGTGACACCACAGCTCAGCTCCCCAGCACCGCTGTGTCTGACACTGCAGGAG AGGCTGCTGGCCTTCGAGCGGGACCGTGTGACCATCCCAGCAGCCCAGGTGGCTTTGGCC AAACAGCTGGCTGGCGACATCGCCCTGGAGCTGCAGGCCTACTTTCGGAGCAAGTTCCCG GAACTGCCCTTTGGGGCATTCGTGCCTGGGGGGCCGCTCTACGACGGGCTGCAGGCGGGG GCTGCGGACCATGTGCGTCTCCTGGTGCCACTGGTGCTGGAGCCGGGCCTGTGGAGCCTG GTGCCGGGCGTGGACACTGTGGCGAGGGACCCTCGCTGCTGGGCCGTGCGCAGGACGCAG CTTGAGTTCTGCCCCCGTGGGAGCAGCCCCTGGGACCGCTTCCTGGTCGGGGGCTACCTC TCCTCCCGCGTCCTGCTGGAGCTACTCCGCAAGGCGCTGGCTGCTTCTGTCAACTGGCCG GCCATTGGCAGCCTTCTCGGGTGCCTGATCCGGCCCAGCATGGCCTCGGAGGAGCTGCTG CTCGAGGTGCAGCACGAACGCCTGGAGCTCACTGTGGCTGTGCTTGTGGCAGTCCCTGGG GTCGATGCTGACGACCGCCTCCTCTTGGCCTGGCCCCTGGAGGGGCTGGCGGGGAACCTC TGGCTGCAGGACCTGTATCCAGTGGAGGCTGCTAGGCTGCGAGCCCTGGACGACCATGAC GCTGGGACTCGCCGGCGGCTGCTGCTGCTGCTGTGTGCTGTCTGCCGTGGTTGCTCGGCT CTGGGGCAGCTAGGCCGGGGTCACCTGACCCAGGTGGTCCTGCGTCTGGGGGAGGACAAC GTGGATTGGACGGAGGAGGCCTTGGGTGAGCGCTTCCTGCAAGCCCTGGAGCTGCTCATC GGCAGCCTGGAGCAGGCCAGCCTGCCCTGCCACTTCAACCCCAGCGTGAACCTCTTCAGC AGCTTGCGTGAGGAGGAGATTGACGACATTGGCTATGCGCTATACAGTGGCCTACAGGAG CCCGAGGGGCTGCTCTAG |
| Restriction Sites | Please inquire |
| ACCN | NM_148886 |
| 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_148886.1, NP_683684.2 |
| RefSeq Size | 2458 bp |
| RefSeq ORF | 1398 bp |
| Locus ID | 125170 |
| UniProt ID | Q96C03 |
| Protein Families | Transmembrane |
| Gene Summary | This gene encodes an outer mitochondrial membrane protein that functions in the regulation of mitochondrial morphology. It can directly recruit the fission mediator dynamin-related protein 1 (Drp1) to the mitochondrial surface. The gene is located within the Smith-Magenis syndrome region on chromosome 17. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jun 2011] Transcript Variant: This variant (2) differs in the 5' UTR and uses a distinct translational start codon, compared to variant 1. The resulting isoform (2) is longer at the N-terminus, compared to isoform 1. |
Documents
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| FAQs |
| SDS |
Resources
Other Versions
| SKU | Description | Size | Price |
|---|---|---|---|
| RC204905 | SMCR7 (Myc-DDK-tagged)-Human Smith-Magenis syndrome chromosome region, candidate 7 (SMCR7), transcript variant 2 |
CNY 3990.00 |
|
| RC204905L3 | Lenti-ORF clone of SMCR7 (Myc-DDK-tagged)-Human Smith-Magenis syndrome chromosome region, candidate 7 (SMCR7), transcript variant 2 |
CNY 5890.00 |
|
| RC204905L4 | Lenti-ORF clone of SMCR7 (mGFP-tagged)-Human Smith-Magenis syndrome chromosome region, candidate 7 (SMCR7), transcript variant 2 |
CNY 5890.00 |
|
| RG204905 | SMCR7 (tGFP-tagged) - Human Smith-Magenis syndrome chromosome region, candidate 7 (SMCR7), transcript variant 2 |
CNY 7456.00 |
