LHR is the receptor for both luteinizing hormone and choriogonadotropin. It belongs to the G protein-coupled receptor 1 family. Mutations in LHR result in disorders of male secondary sexual character development, including familial male precocious puberty, also known as testotoxicosis, hypogonadotropic hypogonadism, Leydig cell adenoma with precocious puberty, and male pseudohermaphtoditism with Leydig cell hypoplasia.
Mouse LHR (NP_038610) VersaClone cDNA
R&D Systems | Catalog # RDC0684
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Formulation, Preparation, and Storage
Shipping
The product is shipped at ambient temperature. Upon receipt, store it immediately at the temperature recommended below.
Storage
Store the unopened product at -20 to -70 °C. Use a manual defrost freezer and avoid repeated freeze-thaw cycles. Do not use past expiration date.
Background: LHR
Long Name
Luteinizing Hormone Receptor/Choriogonadotropin Receptor
Alternate Names
CGR, HHG, LCGR, LGR2, LHCGR, ULG5
Gene Symbol
LHCGR
UniProt
Additional LHR Products
Product Documents for Mouse LHR (NP_038610) VersaClone cDNA
Certificate of Analysis
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Note: Certificate of Analysis not available for kit components.
Product Specific Notices for Mouse LHR (NP_038610) VersaClone cDNA
For research use only
Related Research Areas
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