AMHR2 (NM_020547) Human Tagged ORF Clone Lentiviral Particle
CAT#: RC212425L3V
- LentiORF®
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Lenti ORF particles, AMHR2 (Myc-DDK tagged) - Human anti-Mullerian hormone receptor, type II (AMHR2), transcript variant 1, 200ul, >10^7 TU/mL
Lentiviral Particles: DDK mGFP mGFP w/ Puro
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Specifications
Product Data | |
Type | Human Tagged ORF Clone Lentiviral Particle |
Tag | Myc-DDK |
Symbol | AMHR2 |
Synonyms | AMHR; MISR2; MISRII; MRII |
Mammalian Cell Selection | Puromycin |
Vector | pLenti-C-Myc-DDK-P2A-Puro |
ACCN | NM_020547 |
ORF Size | 1722 bp |
Sequence Data |
The ORF insert of this clone is exactly the same as(RC212425).
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OTI Disclaimer | The molecular sequence of this clone aligns with the gene accession number as a point of reference only. However, individual transcript sequences of the same gene can differ through naturally occurring variations (e.g. polymorphisms), each with its own valid existence. This clone is substantially in agreement with the reference, but a complete review of all prevailing variants is recommended prior to use. More info |
OTI Annotation | This clone was engineered to express the complete ORF with an expression tag. Expression varies depending on the nature of the gene. |
Reference Data | |
RefSeq | NM_020547.1 |
RefSeq Size | 1855 bp |
RefSeq ORF | 1722 bp |
Locus ID | 269 |
UniProt ID | Q16671 |
Cytogenetics | 12q13.13 |
Protein Families | Druggable Genome, Protein Kinase, Transmembrane |
Protein Pathways | Cytokine-cytokine receptor interaction, TGF-beta signaling pathway |
MW | 62.6 kDa |
Gene 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] |
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