Hydroxysteroid (17 beta) Dehydrogenase 4 (HSD17B4) (NM_000414) Human 3' UTR Clone
CAT#: SC204821
3' UTR clone of hydroxysteroid (17-beta) dehydrogenase 4 (HSD17B4) 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 | Hydroxysteroid (17 beta) Dehydrogenase 4 (HSD17B4) (NM_000414) Human 3' UTR Clone |
Vector | pMirTarget |
Synonyms | DBP; MFE-2; MFP-2; MPF-2; PRLTS1; SDR8C1 |
ACCN | NM_000414 |
Insert Size | 368 bp |
Sequence Data |
>SC204821 3’UTR clone of NM_000414
The sequence shown below is from the reference sequence of NM_000414. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC ATGATTCTTAAAGACTACGCCAAGCTCTGAAGGGCACACTACACTATTAATAAAAATGGAATCATTAAA TACTCTCTTCACCCAAATATGCTTGATTATTCTGCAAAAGTGATTAGAACTAAGATGCAGGGGAAATTG CTTAACATTTTCAGATATCAGATAACTGCAGATTTTCATTTTCTACTAATTTTTCATGTATCATTATTT TTACAAGGAACTATATATAAGCTAGCACATAATTATCCTTCTGTTCTTAGATCTGTATCTTCATAATAA AAAATTTTGCCCAAGTCCTGTTTCCTTAGAATTTGTGATAGCATTGATAAGTTGAAAGGAAAATTAAAT CAATAAAGGCCTTTGATACCTTT 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_000414.4 |
Synonyms | DBP; MFE-2; MFP-2; MPF-2; PRLTS1; SDR8C1 |
Summary | The protein encoded by this gene is a bifunctional enzyme that is involved in the peroxisomal beta-oxidation pathway for fatty acids. It also acts as a catalyst for the formation of 3-ketoacyl-CoA intermediates from both straight-chain and 2-methyl-branched-chain fatty acids. Defects in this gene that affect the peroxisomal fatty acid beta-oxidation activity are a cause of D-bifunctional protein deficiency (DBPD). An apparent pseudogene of this gene is present on chromosome 8. Multiple alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, May 2014] |
Locus ID | 3295 |
MW | 14.2 |
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