FSHR Polyclonal Antibody, 100ul[BT-AP03379] Enzyme Activity Assays Localizes to the cell cortex

Localizes to the cell cortex and this requires ERC1 and PHLDB2

Several transcript variants encoding different isoforms have been found for MEF2A

Defects in this gene are the cause of LIG4 syndrome

and a role in the stable assembly of the outer kinetochore

and that shares similarity with the intercellular adhesion molecule (ICAM) protein family

FSHR Polyclonal Antibody, 100ul[BT-AP03379] Enzyme Activity Assays Localizes to the cell cortexFollicle stimulating hormone receptor encoded by FSHR 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.