FSH Receptor (FSHR) (NM_181446) Human 3' UTR Clone
CAT#: SC207656
3' UTR clone of follicle stimulating hormone receptor (FSHR) transcript variant 2 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 | FSH Receptor (FSHR) (NM_181446) Human 3' UTR Clone |
Vector | pMirTarget |
Synonyms | FSHR1; FSHRO; LGR1; ODG1 |
ACCN | NM_181446 |
Insert Size | 606 bp |
Sequence Data |
>SC207656 3’UTR clone of NM_181446
The sequence shown below is from the reference sequence of NM_181446. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC GTCCCTCTAAGTCATTTAGCCCAAAACTAAAACACAATGTGAAAATGTATCTGAGTATTGAATGATAAT TCAGTCTTGCCTTTGAAGGGTATGTCACAAAGAGCTGACAGTGCTTCTACACATTTCATCTAATTTAAT ATTCCTGGCATACCTTTAAGGTAAATTGGTCAGGAACTATTAATTCCATGTGATACATTAGGAAGCTGA ATTATTAGTAACAACAATAATAATTAAAGAATGCAATACTGTATTACATATTTTATCCTTATATATGTT ATTTTTGCACGTTATGTTCAAAGTGCTTTTGTTCAGATATCTCAAGTGATCCCTGTTAAATAAGCAGGA CAGGGATTATTCTTGGAGTTTTACAAATGAGGAAACCACGACTCAAAGAGTTAAGTGACTTGTTCAAAA TTGTTTAGTTTGTAAGAGGCAGAGCCAGGATTAGGTATTCCGACTCCCAGAGAATTTCCCAGAGAAGCA CCATGGTATTCATTCATTCATTCATTCAACAAATATTAATTGAACACCCATCTGAAGCCTTTGTAATGC GTCAGTGTGGATAGGCTGAAATACATTTCCCAGATTTCCCTTCCTCATGTGTTT 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_181446.3 |
Synonyms | FSHR1; FSHRO; LGR1; ODG1 |
Summary | The protein encoded by this gene belongs to family 1 of G-protein coupled receptors. It is the receptor for follicle stimulating hormone and functions in gonad development. Mutations in this gene cause ovarian dysgenesis type 1, and also ovarian hyperstimulation syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2010] |
Locus ID | 2492 |
MW | 22.9 |
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