RFX5 (NM_001025603) Human 3' UTR Clone
CAT#: SC215218
3' UTR clone of regulatory factor X 5 (influences HLA class II expression) (RFX5) transcript variant 2 for miRNA target validation
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CNY 5,795.00
货期*
3周
规格
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经常一起买 (2)
Specifications
Product Data | |
Product Name | RFX5 (NM_001025603) Human 3' UTR Clone |
Vector | pMirTarget |
ACCN | NM_001025603 |
Insert Size | 1576 bp |
Sequence Data |
>SC215218 3’UTR clone of NM_001025603
The sequence shown below is from the reference sequence of NM_001025603. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC CATAAAGACCCAAAAGCAACACCCCCATGATACAGGTCTGTGGGGAAGAGTGTTTATATCCCTACGTTA ACTTTGCCTAGTAGAGGCCCTTCTTTGCACTTGCTTCTCATTTGGCTATTCTTTTCCTAAGGAAGTCCA TTCTCCTCTGTACAGACAGCTGAGTCACCCAGTCTACTTAGTACCTGGTTGCTGCCTCTGACCTTTTCA GCTTGATACCCTGGGCTTTAGTGTAACCAATAAATCTGTAGTGACCTTACCTGTATTCCCTGTGCTATC CTGTGGGAAGGTAGGAATGGGCTAAGTATGATGAATATATAGGTTAGGGATCTTTTGGTTTTAAATCAC AGAAAACCTAATTCAAACTGGCTTAAAATAAAAAGGATTTATTGGTTCATGTAACTAGAAAGTCCATAG GTAGTGCTGGCTCCAGGTGAAGACTTGACCCAGTAGTTCAGTATGTCTCTAAATACCGGACTGACTTTT TTCTCACTGTTGCATCTTCTGTAGGACCATTTAAGTCTGGGCCACTTAATGGCTGCCAGCATTCCTAAG ATTACACTTTTCCCCATTTATGTCCAATCAGAAAAAGAAGGCATCTTTGTACCAGAAATCTCAGCAAAA GCCCTAATATTCACACTGATTAGGCCTGGGTCACATGTCCACCCTGACCAATCACTGTGGCCAGGAGGA TGATACATGCTAATTTGCTTATTCTATATCATGGACAACACCTTTGGGGAAAAGGGTGGGGGTCAGCCT CCCCAAAATCACATGGATTCCCCAAGTGGAAACTAGGAGCAGGGAGTTGCTTGGGTGGCCGCTAACACC AGGCTACTCTTATTTTAGCTTGCTAAGTTGAGATCAGCTAGACCTGCTTTCTTTTCTCCTCAGTCTTGC ATTTCCCTCAATACAAGCTGTAGCCTCTTTCCTCGTTTCTAGTCTCAGAAGGAAGGAGAGGGAAGCCAT TCTCCTCTAGGGACTCTTCAGTCTCATTTAGATGATAGTCCCTTTTTTTCTACCTCCATATTAGAGATG GAGCTCCTTCCTTTTCCTGTTTCTTAATTTTTGTCTTCTCATTCCTGCTTCCCTCTCACCCTATTGCCA GTTCCACCAACTAGAGTGAAAGACTTCCTAGCCATTTCATTAAATCTATTCTGTATCCACCAGGTGGCA GCATCTTGTCATACGTGTCAGGACTTAGGACTGCGGGGTTTAGGTTAGATGTCACGGAAAAAGCTAGTT CTGTGGTCAGGCGGCACCAATGAGAAAGGAATGCAGACCCTCCAGATGTATCCTTGGGAAAAGCAGTAA ACCAACTAATATTTATTGAAGACCTACTTTGTCCTCTACATAGGGTAGCTTCTGTCAGGGAATCTTGGT TCTTCCCAAGAAACACTGATTTTCTTTCAGGGAGACTTCATGTGTTCATTTATTTCCACCACAGCAGAT TTTAAGAAATTATAATATGTAATATTTGATATCTATAAAGAGTATATCTAACGTGAATAAATTATGAAG CATACTAATGAGTACCTATGACCCATAACACATATACATTAAAACATTTTAAATACCA 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_001025603.2 |
Summary | A lack of MHC-II expression results in a severe immunodeficiency syndrome called MHC-II deficiency, or the bare lymphocyte syndrome (BLS; MIM 209920). At least 4 complementation groups have been identified in B-cell lines established from patients with BLS. The molecular defects in complementation groups B, C, and D all lead to a deficiency in RFX, a nuclear protein complex that binds to the X box of MHC-II promoters. The lack of RFX binding activity in complementation group C results from mutations in the RFX5 gene encoding the 75-kD subunit of RFX (Steimle et al., 1995). RFX5 is the fifth member of the growing family of DNA-binding proteins sharing a novel and highly characteristic DNA-binding domain called the RFX motif. Multiple alternatively spliced transcript variants have been found but the full-length natures of only two have been determined. [provided by RefSeq, Jul 2008] |
Locus ID | 5993 |
MW | 59 |
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