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EVC2 (NM_001166136) Human Untagged Clone
CAT＃: SC327289
EVC2 (untagged)-Human Ellis van Creveld syndrome 2 (EVC2) transcript variant 2
CNY 23,660.00
Product images
Specifications
| Product Data | |
| Type | Human Untagged Clone |
| Tag | Tag Free |
| Synonyms | LBN; WAD |
| Vector | pCMV6-XL5 |
| E. coli Selection | Ampicillin (100 ug/mL) |
| Mammalian Cell Selection | None |
| Sequence Data |
>NCBI ORF sequence for NM_001166136, the custom clone sequence may differ by one or more nucleotides
ATGATTTGGCCCAAAGTGGAATGCTGTCACTTTAAGACTGCAGTGGAAGCACCACTTGGA ATGAAATTGGACAAGAAAATGGAAGTCTTCATCCCACTCTCAACTTCTGCAGCCTCTAGT GGGCCATGGGCTCATTCCTTATTTGCTTTTATACCCTCCTGGCCTAAGAAGAACTTATTT AAAAGAGAGTCTCCTATAACACACCGCCTGTATGGGGACATTTCAAGAGAAGTTCAAGGG ACTTCTGAAAATGGAGTAATTTTTCAGAAATGTGCACTGGTGTCTGGGTCGAGTGAAGCA CAGACAGCCCGCATATGGCTGCTTGTTAACAACACCAAGACAACCTCGTCAGCCAACCTC TCGGAGCTGCTCTTGCTGGACAGCATTGCTGGTCTCACCATTTGGGACTCTGTGGGAAAC AGGACCTCGGAAGGATTCCAGGCTTTTAGCAAGAAGTTTCTGCAAGTGGGAGATGCCTTT GCTGTCAGCTACGCAGCCACGCTCCAGGCTGGAGACCTCGGGAACGGGGAGAGCCTCAAG CTTCCTGCCCAACTCACCTTTCAGAGCTCGTCACGGAACAGAACACAGCTGAAAGTGCTT TTTTCCATAACAGCAGAAGAAAACGTAACGGTTCTGCCGCACCACGGCCTCCACGCAGCA GGGTTCTTCATTGCCTTCCTCCTCTCCCTTGTGCTGACCTGGGCTGCCCTCTTCCTCATG GTTCGCTATCAGTGTCTGAAGGGAAACATGCTCACCAGACATCGGGTTTGGCAGTATGAG AGCAAGCTGGAACCCTTGCCGTTCACCTCAGCTGATGGCGTGAATGAGGACCTTTCCCTT AACGACCAAATGATAGACATTCTGTCTTCCGAGGACCCTGGGAGCATGCTTCAAGCCTTA GAAGAGTTGGAGATTGCAACCCTGAATCGGGCAGATGCAGATCTGGAGGCTTGTCGAACA CAAATCAGCAAGGATATCATTGCCCTTCTGCTGAAAAATCTCACCAGCAGTGGCCACCTC TCACCCCAAGTAGAGAGAAAAATGAGTGCTGTTTTCAAAAAGCAGTTTCTATTGCTGGAA AATGAAATACAAGAGGAGTACGATCGGAAGATGGTGGCATTGACAGCTGAATGTGACCTG GAAACAAGAAAGAAGATGGAAAACCAGTACCAGAGAGAGATGATGGCAATGGAGGAAGCA GAAGAGTTGCTGAAACGTGCTGGTGAGAGGTCTGCTGTAGAGTGCAGCAACCTTCTGCGG ACCCTCCATGGCCTGGAACAGGAGCACTTGAGGAAGTCTCTCGCTTTGCAACAAGAAGAA GACTTTGCCAAAGCTCACAGACAGCTGGCTGTTTTCCAGAGAAATGAACTGCACAGTATC TTTTTTACCCAGATAAAAAGTGCTATTTTCAAAGGGGAATTGAAACCAGAGGCAGCTAAA ATGCTGCTGCAAAATTATTCTAAAATACAGGAGAATGTAGAAGAGTTAATGGACTTTTTC CAGGCTAGTAAGAGGTATCATCTAAGTAAAAGATTTGGCCACAGGGAATATCTGGTCCAG AACCTCCAGTCATCAGAGACCCGTGTGCAGGGCCTTCTGAGCACCGCTGCAGCCCAGCTG ACTCACCTCATTCAGAAGCACGAGAGAGCAGGGTACCTGGATGAAGACCAAATGGAAATG CTATTGGAGCGGGCTCAGACAGAAGTCTTTTCAATCAAGCAGAAGTTGGACAATGACTTA AAGCAGGAAAAGAAAAAGCTCCACCAAAAATTAATAACTAAGAGAAGACGAGAGTTGCTA CAAAAGCACAGGGAGCAGCGTAGGGAGCAGGCGTCCGTCGGCGAGGCCTTCCGAACGGTT GAGGATGCCGGCCAGTACCTGCACCAGAAGAGGAGCCTGATGGAGGAGCACGGTGCCACC CTGGAGGAGCTGCAGGAGCGTCTGGACCAGGCCGCCCTGGACGATCTCAGGACCCTGACC CTTTCGCTGTTTGAAAAGGCCACCGACGAGCTGCGGCGCCTGCAGAACTCAGCCATGACC CAGGAGCTGCTCAAGCGTGGGGTGCCCTGGCTCTTCCTGCAGCAGATCCTGGAGGAGCAC GGCAAGGAGATGGCTGCACGGGCCGAGCAGCTGGAGGGGGAGGAGAGGGACAGGGACCAG GAGGGTGTCCAGAGCGTGAGGCAGAGACTGAAGGATGACGCTCCTGAGGCCGTGACAGAG GAGCAGGCAGAGCTGCGACGCTGGGAGCACCTGATCTTCATGAAGCTCTGCTCCTCAGTC TTCTCCCTGTCTGAAGAGGAGCTGCTCAGGATGAGGCAGGAGGTCCATGGCTGCTTTGCT CAGATGGACAGGAGCTTGGCCCTCCCCAAGATCCGGGCCCGAGTTCTGCTGCAGCAATTT CAGACTGCGTGGCGAGAAGCAGAGTTCGTGAAGCTGGACCAGGCCGTGGCTGCCCCTGAG CTGCAGCAACAGTCCAAGGTGAGAAAGTCACGGTCCAAGAGTAAAAGCAAGGGAGAGCTT CTGAAGAAGTGCATCGAAGACAAAATTCACCTCTGTGAGGAACAGGCCTCTGAAGACCTG GTGGAAAAGGTTCGAGGTGAATTGCTGCGGGAGAGAGTGCAGCGGATGGAGGCACAGGAG GGAGGCTTTGCACAGTCGCTTGTTGCTCTGCAGTTCCAGAAGGCGTCCCGGGTGACCGAG ACTCTGTCGGCCTACACCGCCCTCCTCAGCATCCAGGACTTGCTCCTGGAAGAGCTGAGT GCATCTGAGATGCTGACCAAGTCGGCCTGCACACAGATCCTGGAGTCGCACAGCCGGGAG CTCCAGGAGTTGGAGAGGAAGCTGGAGGACCAGCTGGTGCAGCAGGAGGCAGCCCAGCAG CAGCAGGCCCTGGCGAGCTGGCAGCAGTGGGTGGCCGATGGGCCCGGGATTCTGAACGAA CCTGGGGAGGTGGATTCTGAAAGGCAGGTCTCTACTGTCCTGCACCAAGCCCTGAGCAAG AGCCAGACATTACTGGAGCAACATCAGCAGTGTTTGAGAGAGGAACAACAGAACAGTGTC GTGCTAGAAGACTTGTTGGAAAACATGGAGGCAGACACCTTTGCAACCCTGTGCAGCCAG GAGCTGAGACTGGCATCGTACCTGGCGAGGATGGCCATGGTGCCCGGGGCCACGCTTCGC CGGCTCCTGAGTGTGGTACTGCCCACAGCCTCACAGCCTCAGCTGCTGGCCCTGCTGGAT TCGGCCACCGAGAGACATGTGGACCACGCAGCTGAGAGCGATGGCGGAGCGGAGCAGGCC GACGTGGGCAGGCGGAGGAAACACCAGAGCTGGTGGCAAGCCTTAGATGGCAAACTGCGA GGAGATCTGATAAGCAGAGGATTAGAAAAGATGCTGTGGGCCCGCAAGAGAAAGCAGAGC ATATTAAAGAAGACATGTCTCCCTCTCAGAGAGAGGATGATATTCTCTGGAAAAGGAAGT TGGCCACACCTGTCACTGGAGCCCATTGGCGAACTGGCCCCTGTACCCATTGTAGGGGCA GAAACCATTGATCTATTAAACACAGGAGAGAAGCTCTTTATATTCAGAAATCCAAAGGAG CCAGAGATCTCACTGCACGTTCCTCCCAGGAAAAAGAAGAACTTTTTGAATGCCAAAAAG GCCATGAGGGCCTTGGGCATGGAC |
| Restriction Sites | Please inquire |
| ACCN | NM_001166136 |
| 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_001166136.1, NP_001159608.1 |
| RefSeq Size | 4864 bp |
| RefSeq ORF | 3687 bp |
| Locus ID | 132884 |
| UniProt ID | Q86UK5 |
| Protein Families | Transmembrane |
| Gene Summary | This gene encodes a protein that functions in bone formation and skeletal development. Mutations in this gene, as well as in a neighboring gene that lies in a head-to-head configuration, cause Ellis-van Creveld syndrome, an autosomal recessive skeletal dysplasia that is also known as chondroectodermal dysplasia. Mutations in this gene also cause acrofacial dysostosis Weyers type, also referred to as Curry-Hall syndrome, a disease that combines limb and facial abnormalities. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2009] Transcript Variant: This variant (2) differs in the 5' UTR, lacks a portion of the 5' coding region, and uses a downstream translational start codon, compared to variant 1. The resulting isoform (2) is shorter at the N-terminus, compared to isoform 1. |
Documents
| Product Manuals |
| FAQs |
| SDS |
Resources
Other Versions
| SKU | Description | Size | Price |
|---|---|---|---|
| RC228654 | EVC2 (Myc-DDK-tagged)-Human Ellis van Creveld syndrome 2 (EVC2), transcript variant 2 |
CNY 8,552.00 |
|
| RC228654L3 | Lenti-ORF clone of EVC2 (Myc-DDK-tagged)-Human Ellis van Creveld syndrome 2 (EVC2), transcript variant 2 |
CNY 14,160.00 |
|
| RC228654L4 | Lenti-ORF clone of EVC2 (mGFP-tagged)-Human Ellis van Creveld syndrome 2 (EVC2), transcript variant 2 |
CNY 14,160.00 |
|
| RG228654 | EVC2 (tGFP-tagged) - Human Ellis van Creveld syndrome 2 (EVC2), transcript variant 2 |
CNY 13,490.00 |
