LONP1 (NM_004793) Human 3' UTR Clone
CAT#: SC202206
3' UTR clone of lon peptidase 1 mitochondrial (LONP1) nuclear gene encoding mitochondrial protein 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 | LONP1 (NM_004793) Human 3' UTR Clone |
Vector | pMirTarget |
Synonyms | CODASS; hLON; LON; LonHS; LONP; PIM1; PRSS15 |
ACCN | NM_004793 |
Insert Size | 228 bp |
Sequence Data |
>SC202206 3’UTR clone of NM_004793
The sequence shown below is from the reference sequence of NM_004793. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC CAGGCAGAGGCGCTGGCCGTGGAACGGTGACGGCCACCCCGGGACTGCAGGCGGCGGATGTCAGGCCCT GTCTGGGCCAGAACTGAGCGCTGTGGGGAGCGCGCCCGGACCTGGCAGTGGAGCCACCGAGCGAGCAGC TCGGTCCAGTGACCCAGATCCCAGGGACCTCAGTCGGCTTAATCAGAGTGTGGCATAGAAGCTATTTAA TGATTAAAGTCATTTGCAGTA 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_004793.4 |
Synonyms | CODASS; hLON; LON; LonHS; LONP; PIM1; PRSS15 |
Summary | This gene encodes a mitochondrial matrix protein that belongs to the Lon family of ATP-dependent proteases. This protein mediates the selective degradation of misfolded, unassembled or oxidatively damaged polypeptides in the mitochondrial matrix. It may also have a chaperone function in the assembly of inner membrane protein complexes, and participate in the regulation of mitochondrial gene expression and maintenance of the integrity of the mitochondrial genome. Decreased expression of this gene has been noted in a patient with hereditary spastic paraplegia (PMID:18378094). Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Feb 2013] |
Locus ID | 9361 |
MW | 8.6 |
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