MCCC2 (NM_022132) Human 3' UTR Clone
CAT#: SC216796
3`UTR clone of methylcrotonoyl-Coenzyme A carboxylase 2 (beta) (MCCC2) nuclear gene encoding mitochondrial protein for miRNA target validation
Product Images
![](https://cdn.origene.com/img/defaults-img.jpg)
Other products for "MCCC2"
Specifications
Product Data | |
Vector | pMirTarget |
Species | Human |
Transfection Reporter | RFP |
Assay Reporter | Luciferase |
E. coli Selection | Kanamycin (25 ug/mL) |
Mammalian Cell Selection | Neomycin |
Symbol | MCCC2 |
Synonyms | MCCB |
ACCN | NM_022132 |
Insert Size | 1858 |
Sequence Data |
>SC216796 3'UTR clone of NM_022132
The sequence shown below is from the reference sequence of NM_022132. The complete sequence of this clone may contain minor differences, such as SNPs. Red=Cloning site Blue=Stop Codon CAATTGGCAGAGCTCAGAATTCAAGCGATCGC CGCACCAATAGAGAAGACTGACTTCGGTATCTTCAGGATGTAACTGGAATAAAGGATGTTTTCTGTTGGA CATGTACTGAAAATTAACACATGTAGTAGCCTTAAAATTTTAGACTTCTCGAACATGAGGCTGTTACAGT AATTTTTTTAACACTGTGCATTGTACTTTTCTACCTTAAAAAAATCAGTGAGGATATTTATTTAATGAAC ATCAATTCCTTTTAAATTTTCTTAGAGAAATTTCTCTGTGGCTCAGTTTTACCACCCATAAAGCGGAGAC AGTAATTTACGGTTATCCTTTCTGACCCACAAAGTATGAAAAGTTCTGTAATCTGTAAACTCAGTTCTGT AATCTGTATTATTGAGATGATTAATATAAAGTTGTATTTTCACTGAAATGATTGTTTTGCTGGTTATGCT TGGTGATATTTTAGCGGGCTTATTTTTGAAAGGCATCTGTTACTTCAGTGGCATAAAGTGCCCTCACACT GCTGTGCAGCCATCACCACCATTCATCTCCAGAATTTGTTCTCAGTCCCAAACTGAAACTATACCATTCA AACAACAGCGCTCCCCATTTCCCCCTCCCCCGAGCCCATGACATCTCCTTATTATTATTTTTTTTTTGAG ACAGGGTGTTTCTCTGTTGCCCAGGCTGGAGTGCGGTGGTGTGATCTCGGCTCACTGCAGCTTCCACCTC CCGGGTTCAAGCGATTCTTGTGCCTCAGCCTCCCAAGCAGCTGGGACTATAGGCACGCACCACCACACCC AGCTAAGTTCTGTATTTTTAGCAGAGACGGGATTTCACTAGGTTGCCCAGGCTGGTCTCAAACTACTGAC CTCAAGTGATCCACCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCGCGCCTGACCA CATCTCCTTATTCTTAAATGTATGTGTTTCTCATGGTTTGATTTATTCTTGCTGGGCCATTTCAGCCCCT GTCATGGCTTCACTCGCCATCTAAATGCAGATGATTACTGCCTTGACGGTTCTTAACCCAGCTCTCCCCT GAGCTGCAGGCCTGCATATCCAGTAGGTCTACTGGACATCTGTACTGGTTGTTGTGGAGGAACCTCTGGC TTGCTCATTAAGTCCTACTGATTTTCACTATCCCCTGAATTTCCCCACTTATTTTTGTCTTTCACTATCG CAGGCCTTAGAAGAGGTCTACCTGCCTCCAGTCTTACCTAGTCCAGTCTACCCCCTGGAGTTAGAATGGC CATCCTGAAGTGAAAAGTAATGTCAGATTACTCCCTTCAGTGATTTCTTGTAGAAGTGCCAATCCCTGAA TGCCACCAAGATCTTAATCTTCACATCTTTAATCTTATCTCTTTGACTCCTCTTTACACCGGAGAACGGC TCCAGCTGTTCTAGCTCTCTTTCAGTTCTTTGAACCTTCCCACCTTAGGGTCTATAAGGTTCCCTCTGCC CAAATTGTTCTACTCTCCCTTCTTCTTCAACACATCCTTCAGTTTAAGCACTTGCTTCTCTCAGTTTAAA CTCCACTTCCTTAGGGATGTCTCTGTGACCTCCCTGTGCTGGATTAGCTTCCCTACTCTATGCTCTTGTA AAACACTATCTACTTCCTTTGTCATAAACTCATCATTTTCCTATAAACATTAATATTGTCCTCCTGCTAG AATGTAAGCTCCGTGAGAGCAAGGATCCTCCTGTTTACCCTGTACCTCCAATGTCTGGCACTTGTAGGTG CTCAAATATTCGTTGAATGAATGAAAAATCCATATTGTAATTGATGTCCTCTGGCCACATAGTTTTAAAA TTAGGTGATTGATTATATGACCGAATAGAACTATCAAA ACGCGTAAGCGGCCGCGGCATCTAGATTCGAAGAAAATGACCG |
Restriction Sites | SgfI-MluI |
OTI Disclaimer | Our molecular clone sequence data has been matched to the sequence identifier above as a point of reference. Note that the complete sequence of this clone is largely the same as the reference sequence but may contain minor differences , e.g., single nucleotide polymorphisms (SNPs). |
Reference Data | |
RefSeq | NM_022132.4 |
Summary | This gene encodes the small subunit of 3-methylcrotonyl-CoA carboxylase. This enzyme functions as a heterodimer and catalyzes the carboxylation of 3-methylcrotonyl-CoA to form 3-methylglutaconyl-CoA. Mutations in this gene are associated with 3-Methylcrotonylglycinuria, an autosomal recessive disorder of leucine catabolism. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, May 2018] |
Locus ID | 64087 |
Documents
Product Manuals |
FAQs |
SDS |
Resources
{0} Product Review(s)
0 Product Review(s)
Submit review
Be the first one to submit a review
Product Citations
*Delivery time may vary from web posted schedule. Occasional delays may occur due to unforeseen
complexities in the preparation of your product. International customers may expect an additional 1-2 weeks
in shipping.