AMHR2 (NM_020547) Human 3' UTR Clone

CAT#: SC200131

3' UTR clone of anti-Mullerian hormone receptor type II (AMHR2) transcript variant 1 for miRNA target validation



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CNY 4,845.00


货期*
3周

规格
    • 10 ug

Cited in 1 publication.

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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 AMHR2 (NM_020547) Human 3' UTR Clone
Vector pMirTarget
Synonyms AMHR; MISR2; MISRII; MRII
ACCN NM_020547
Insert Size 229 bp
Sequence Data
>SC200131 3’UTR clone of NM_020547
The sequence shown below is from the reference sequence of NM_020547. The complete sequence of this clone may contain minor differences, such as SNPs.
Blue=Stop Codon Red=Cloning site

GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG
TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC
CAGCCTGCCTGTACCCTTTCTCCTGTGTAAATATGCAGTTTATGTGTCATCAATGTACATGCCAACATA
AATATGGCGATTGTATAGCTGTCTTGTCTGCCTCATCACTGCATTTCCCACCTGCCGAATCCTTGGATT
CTTCTGCGGGCATCCAGTCCACATCAGTTCTGACCAGTGACTTGGGGTAGGTGTGCACAGGAAAGAGAA
TAAAGTCAGCTTTCCTGATGCA
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_020547.3
Synonyms AMHR; MISR2; MISRII; MRII
Summary This gene encodes the receptor for the anti-Mullerian hormone (AMH) which, in addition to testosterone, results in male sex differentiation. AMH and testosterone are produced in the testes by different cells and have different effects. Testosterone promotes the development of male genitalia while the binding of AMH to the encoded receptor prevents the development of the mullerian ducts into uterus and Fallopian tubes. Mutations in this gene are associated with persistent Mullerian duct syndrome type II. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Sep 2009]
Locus ID 269
MW 8.4
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Citations (1)

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