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
    • 10 ug

Product images

经常一起买 (2)
Firefly luciferase assay kit, 150 assays
    • 1 kit

CNY 1,520.00


DH5α Chemically Competent Cells (≥10^8 cfu/μg of pUC19 DNA)
    • 5 x 200 ul

CNY 1,280.00

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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