IFNGR1 (NM_000416) Human 3' UTR Clone
CAT#: SC207561
3' UTR clone of interferon gamma receptor 1 (IFNGR1) 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 | IFNGR1 (NM_000416) Human 3' UTR Clone |
Vector | pMirTarget |
Synonyms | CD119; IFNGR; IMD27A; IMD27B |
ACCN | NM_000416 |
Insert Size | 576 bp |
Sequence Data |
>SC207561 3’UTR clone of NM_000416
The sequence shown below is from the reference sequence of NM_000416. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC CCAACAGAAGATTCCAAAGAATTTTCATGAGATCAGCTAAGTTGCACCAACTTTGAAGTCTGATTTTCC TGGACAGTTTTCTGCTTTAATTTCATGAAAAGATTATGATCTCAGAAATTGTATCTTAGTTGGTATCAA CCAAATGGAGTGACTTAGTGTACATGAAAGCGTAAAGAGGATGTGTGGCATTTTCACTTTTGGCTTGTA AAGTACAGACTTTTTTTTTTTTTTAAACAAAAAAAGCATTGTAACTTATGAACCTTTACATCCAGATAG GTTACCAGTAACGGAACAGTATCCAGTACTCCTGGTTCCTAGGTGAGCAGGTGATGCCCCAGGGACCTT TGTAGCCACTTCACTTTTTTTCTTTTCTCTGCCTTGGTATAGCATATGTTTTTGTAAGTTTATGCATAC AGTAATTTTAAGTAATTTCAGAAGAAATTCTGCAAGCTTTTCAAAATTGGACTTAAAATCTAATTCAAA CTAATAGAATTAATGGAATATGTAAATAGAAACGTGTATATTTTTTATGAAACATTACAGTTAGAGATT TTTAAATAAAGAATTTTAAAACTC 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_000416.3 |
Synonyms | CD119; IFNGR; IMD27A; IMD27B |
Summary | This gene (IFNGR1) encodes the ligand-binding chain (alpha) of the gamma interferon receptor. Human interferon-gamma receptor is a heterodimer of IFNGR1 and IFNGR2. A genetic variation in IFNGR1 is associated with susceptibility to Helicobacter pylori infection. In addition, defects in IFNGR1 are a cause of mendelian susceptibility to mycobacterial disease, also known as familial disseminated atypical mycobacterial infection. [provided by RefSeq, Jul 2008] |
Locus ID | 3459 |
MW | 23.2 |
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