Glutathione S Transferase theta 1 (GSTT1) (NM_000853) Human 3' UTR Clone
CAT#: SC203924
3' UTR clone of glutathione S-transferase theta 1 (GSTT1) for miRNA target validation
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CNY 4,845.00
货期*
3周
规格
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Specifications
Product Data | |
Product Name | Glutathione S Transferase theta 1 (GSTT1) (NM_000853) Human 3' UTR Clone |
Vector | pMirTarget |
ACCN | NM_000853 |
Insert Size | 336 bp |
Sequence Data |
>SC203924 3’UTR clone of NM_000853
The sequence shown below is from the reference sequence of NM_000853. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC ATGCCCTGGGTGCTGGCCATGATCCGGTGAGCTGGGAAACCTCACCCTTGCACCGTCCTCAGCAGTCCA CAAAGCATTTTCATTTCTAATGGCCCATGGGAGCCAGGCCCAGAAAGCAGGAATGGCTTGCCTAAGACT TGCCCAAGTCCCAGAGCACCTCACCTCCCGAAGCCACCATCCCCACCCTGTCTTCCACAGCCGCCTGAA AGCCACAATGAGAATGATGCACACTGAGGCCTTGTGTCCTTTAATCACTGCATTTCATTTTGATTTTGG ATAATAAACCTGGGCTCAGCCTGAGCCTCTGCTTCTAACTCTAAAAAAAAAAAAAAAAAA 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_000853.3 |
Summary | The protein encoded by this gene, glutathione S-transferase (GST) theta 1 (GSTT1), is a member of a superfamily of proteins that catalyze the conjugation of reduced glutathione to a variety of electrophilic and hydrophobic compounds. Human GSTs can be divided into five main classes: alpha, mu, pi, theta, and zeta. The theta class includes GSTT1, GSTT2, and GSTT2B. GSTT1 and GSTT2/GSTT2B share 55% amino acid sequence identity and may play a role in human carcinogenesis. The GSTT1 gene is haplotype-specific and is absent from 38% of the population. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Sep 2015] |
Locus ID | 2952 |
MW | 12.2 |
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