PARL (NM_001037639) Human 3' UTR Clone
CAT#: SC202644
3' UTR clone of presenilin associated rhomboid-like (PARL) nuclear gene encoding mitochondrial protein transcript variant 2 for miRNA target validation
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CNY 4,845.00
货期*
3周
规格
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经常一起买 (2)
Specifications
Product Data | |
Product Name | PARL (NM_001037639) Human 3' UTR Clone |
Vector | pMirTarget |
Synonyms | PRO2207; PSARL; PSARL1; PSENIP2; RHBDS1 |
ACCN | NM_001037639 |
Insert Size | 357 bp |
Sequence Data |
>SC202644 3’UTR clone of NM_001037639
The sequence shown below is from the reference sequence of NM_001037639. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC GGCCCCAAAAAAGGAGGTGGCTCTAAGTAAAACTGGGATTGGACAGTAGTGGTGCATCTGGTCCTTGCC GCCTGAGAGCCCCAGGAGACATCGGCTAGAGTGACCATGGCTATGCTCCCGTCTGGAAGATGCCAGCAT CTGGCCTCCCACTGTTTTCAGCTGTGTCCCCCAGTCCGTGTCTTTTTAGAATGTGAATGATGATAAAGT TGTGAAATAAAGGTTTCTATCTAGTTTGTAAGCAGATGTGTGTGTTCTCTCTTTAAGGGGCCGACACGG CTCTGGCATTTTGCTTTGGTTGTTGCATTGACAGGACCTGGGGAGAGTGCACCCTGAAAGGCCTGATCA GAACATGAAGGC ACGCGTAAGCGGCCGCGGCATCTAGATTCGAAGAAAATGACCGACCAAGCGACGCCCAACCTGCCATCA CGAGATTTCGATTCCACCGCCGCCTTCTATGAAAGG |
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_001037639.3 |
Synonyms | PRO2207; PSARL; PSARL1; PSENIP2; RHBDS1 |
Summary | This gene encodes a member of the rhomboid family of intramembrane serine proteases that is localized to the inner mitochondrial membrane. The encoded protein regulates mitochondrial remodeling and apoptosis through regulated substrate proteolysis. Proteolytic processing of the encoded protein results in the release of a small peptide, P-beta, which may transit to the nucleus. Mutations in this gene may be associated with Parkinson's disease. [provided by RefSeq, May 2016] |
Locus ID | 55486 |
MW | 13 |
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