CYB5R3 (NM_001129819) Human 3' UTR Clone

CAT#: SC217089

3' UTR clone of cytochrome b5 reductase 3 (CYB5R3) transcript variant 3 for miRNA target validation



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CNY 5,795.00


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 CYB5R3 (NM_001129819) Human 3' UTR Clone
Vector pMirTarget
Synonyms B5R; DIA1
ACCN NM_001129819
Insert Size 1963 bp
Sequence Data
>SC217089 3’UTR clone of NM_001129819
The sequence shown below is from the reference sequence of NM_001129819. The complete sequence of this clone may contain minor differences, such as SNPs.
Blue=Stop Codon Red=Cloning site

GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG
TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC
CACCCCACGGAGCGCTGCTTCGTCTTCTGAGGGCCGGGCACGGTCACACGGCCACCCGCCCCGCGCACC
CCACGCCCTGTTCACGCTCACCCAGTCACCTCCCCACATCGCACACTGGGGCCCCGGGTTCAGCCTGGC
CTGCCCGTGCCCTGGTGAATCACCTGGCTGAGCAGTTCCCCTGGAGCCCCTTCGGGAGCAGGGCTGTGT
CCCAGATGGGCCACGGCTGAGCCTTCAGAGTACGTCCTGCCTGGCACTTACTGGTCCTTACCAGAGACG
CCCAGCCCCATCCCTGTCCTCATGACCCCTCGTCCACCCCCCACACACACTATAAGGCTGAGGGCTGCC
AGCAGCCCCGTCTGCCCACCATTCCCGGCCGTGGACCATAGTCGGGATGTCAGCAGACACACATGGGCA
GCCCAAAGCTGCAGGTGCCAGGGCCCACCCCAGCCTCGCCTGTCACCCCCACTCCCGCCTCAGGGCCAG
GCCCAGGCCTCACCACCTGACGCTGCATGAGACATTGACACCAGAAAGCCCTCTTGGGGGCACTGCTCC
CTACCCCAGGGCCCTGGCCAGCCGGGAGCTTGGCTCTCCTCTGGCTAGAGTGGGAAGAGGGGGCTGGCC
ATGGGGCCCTCCCAGAACCTCAGCATTTCCTTCCAGCCCATCCAAACACTGAGGCAGCCTTGGGGAACC
CCGAGCTGGGGGGTTGGCAGCCCACTGCACCGCCTCAGGGTTTTGGGGTCCTGGGCTGGGGCCACCATC
CCTGATGGCAGAACTCCCACAACCACATGTATTTATTCCTCTGTCCTAAACCGTCCCCTCCTTCCCTCA
CCCCCAGCACAGGGGGATTCTGAGCAGTGCCTCTTGTCTGAGGGACATATCAGTGACCTCGACGTTGCC
TTTAGACTACAGTTGTGTTAGCCTCTTGCGTATTGGCTTTTTCAGAGTCATTTATGAGCAGAAAAAAAA
AAAGTAAAACTTTGCTAATATTAACCCTTCTCTAGCTCCTCGAGGGTCTGTGACCTGCAACACAAGGGG
TGGGGTCAGGAAAGGGCTGGGGAAGACCTAGCATTTTTTTTTTCTTTTTTTTTTTTTTTTGAGACGGAG
TCTCCCTTTGTCACCCAGGCTGGAGTGGCATGATCTCAGCTCACTACAACCTCCACCTCTCGGGTTCAA
GCGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTAAAAGTGCCCACCACCACACCCAGCTAGTTT
TTGTATTTTTTTTTTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCAGGCTGGAGTGCAGTGGCGG
GATCTCGGCTCACTGCAAGCTCCGCCTCCCGGGTTCACGCCATTCTCCTGCCTCAGCCTCCCAAGTAGC
TGGGACTACAGGCGCCCGCCACTACGCCCGGCTAATTTTTTGTATTTTTAGTAGAGACGGGGTTTCACC
GTTTTAGCCGGGATGGTCTCGATCTCCTGACCTCGTGATCCGCCCGCCTCGGCCTCCCAAAGTGCTGGG
ATTACAGGCGTGAGCCACTGCGCCCGGCTCCAGCATTTATTTCTGATGTATCTTTGTGGTAGAAAATTT
GGAAAGTGCAGAGAAGTATACACAGGAAGAAAAATTCCCAACCCCCAGAGGCAAACCAGCTGAAACCAC
GCAACCCCAGTCACCCCAATGCACCGCGAGGCTGCTGCCTCCTGTCAGGGTCAGATGAGCCTCGAGGCT
CAGGAAAGTCAGAGGATGCCATCTGCATGGTGGTAAATTACAGAGGTGATGAGGCAAGGTGGGTGTGGG
GCTGTTCTTAAAACGGGGCAGCAGGAAGGCCCCAAGGAGATGGATTTGGGCTGGGACGGGAAGAGAGAG
CTGGCCATGCTGGGGTGGGTGGGTGTTCAAATGGTGGAAACAGCAGACGCAAAGGCCCTGCCGTTGGAA
CCAGCTTGTGGAATAAACTTTCAGAAACAGA
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_001129819.2
Synonyms B5R; DIA1
Summary This gene encodes cytochrome b5 reductase, which includes a membrane-bound form in somatic cells (anchored in the endoplasmic reticulum, mitochondrial and other membranes) and a soluble form in erythrocytes. The membrane-bound form exists mainly on the cytoplasmic side of the endoplasmic reticulum and functions in desaturation and elongation of fatty acids, in cholesterol biosynthesis, and in drug metabolism. The erythrocyte form is located in a soluble fraction of circulating erythrocytes and is involved in methemoglobin reduction. The membrane-bound form has both membrane-binding and catalytic domains, while the soluble form has only the catalytic domain. Alternate splicing results in multiple transcript variants. Mutations in this gene cause methemoglobinemias. [provided by RefSeq, Jan 2010]
Locus ID 1727
MW 71.6
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