ALDH3A1 (NM_001135168) Human 3' UTR Clone
CAT#: SC203110
3' UTR clone of aldehyde dehydrogenase 3 family memberA1 (ALDH3A1) transcript variant 1 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 | ALDH3A1 (NM_001135168) Human 3' UTR Clone |
Vector | pMirTarget |
Synonyms | ALDH3; ALDHIII |
ACCN | NM_001135168 |
Insert Size | 282 bp |
Sequence Data |
>SC203110 3’UTR clone of NM_001135168
The sequence shown below is from the reference sequence of NM_001135168. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC CCGAGCCCGGCCAAGATGACCCAGCACTGAGGAGGGGTTGCTCCGCCTGGCCTGGCCATACTGTGTCCC ATCGGAGTGCGGACCACCCTCACTGGCTCTCCTGGCCCTGGGAGAATCGCTCCTGCAGCCCCAGCCCAG CCCCACTCCTCTGCTGACCTGCTGACCTGTGCACACCCCACTCCCACATGGGCCCAGGCCTCACCATTC CAAGTCTCCACCCCTTTCTAGACCAATAAAGAGACGAATACAATTTTCTAACTCAGCAAAAAAAAAAAA AAAAAA 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_001135168.1 |
Synonyms | ALDH3; ALDHIII |
Summary | Aldehyde dehydrogenases oxidize various aldehydes to the corresponding acids. They are involved in the detoxification of alcohol-derived acetaldehyde and in the metabolism of corticosteroids, biogenic amines, neurotransmitters, and lipid peroxidation. The enzyme encoded by this gene forms a cytoplasmic homodimer that preferentially oxidizes aromatic and medium-chain (6 carbons or more) saturated and unsaturated aldehyde substrates. It is thought to promote resistance to UV and 4-hydroxy-2-nonenal-induced oxidative damage in the cornea. The gene is located within the Smith-Magenis syndrome region on chromosome 17. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Sep 2008] |
Locus ID | 218 |
MW | 9.8 |
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