ALDH4A1 (NM_170726) Human 3' UTR Clone
CAT#: SC205619
3' UTR clone of aldehyde dehydrogenase 4 family member A1 (ALDH4A1) nuclear gene encoding mitochondrial protein transcript variant P5CDhS 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 | ALDH4A1 (NM_170726) Human 3' UTR Clone |
Vector | pMirTarget |
Synonyms | ALDH4; P5CD; P5CDh |
ACCN | NM_170726 |
Insert Size | 432 bp |
Sequence Data |
>SC205619 3’UTR clone of NM_170726
The sequence shown below is from the reference sequence of NM_170726. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC GGGGACTGGAGCTACGCGTACATGCAGTGAGCCCCTCTCGGGCTCCACCGTCCAGCTGTCTGTCCGTCC AGATGCCTCCTGCTTGGATTCTGAGTGGTCAGAGATCTGTAAAGCATGACTTTCAAGGATGGTTCTTAG GGGACTGTGAAAGTGTTGGGTCTTCCTCCAGGATGCCTGCATGGGACCCCACCCGGAGCTGGTGTGGCC ATTCCCCAAGTGCCACTGGCCCATGGATGGGGGTGGGTGCTGGTGCCAGCTGGGCTGGGTGTGGGTTCT GTGTCCTTCCAGGATATGTGTCATTTCCCATGAGGGGCCGGGGCAGGTGGCTGGGTGGGGGCACAGGCT GGAGTATTCTTAGTTCTACTGGTTCTACACTGTGAGGTGGCAATGGGATTTGCTCAGATGCCACCCAAT AAAATGCCTGTTACTTAA AGCGGACCGACTTACGCGTAAGCGGCCGCGGCATCTAGATTCGAAGAAAATGACCGACCAAGCGACGCC CAACCTGCCATCACGAGATTTCGATTCCACCGCCGC |
Restriction Sites | SgfI-RsrII |
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_170726.3 |
Synonyms | ALDH4; P5CD; P5CDh |
Summary | This protein belongs to the aldehyde dehydrogenase family of proteins. This enzyme is a mitochondrial matrix NAD-dependent dehydrogenase which catalyzes the second step of the proline degradation pathway, converting pyrroline-5-carboxylate to glutamate. Deficiency of this enzyme is associated with type II hyperprolinemia, an autosomal recessive disorder characterized by accumulation of delta-1-pyrroline-5-carboxylate (P5C) and proline. Alternatively spliced transcript variants encoding different isoforms have been identified for this gene. [provided by RefSeq, Jun 2009] |
Locus ID | 8659 |
MW | 14.8 |
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