FSHR Polyclonal Antibody, 100ul[BT-AP03379] Enzyme Activity Assays disease:Defects in NOTCH1 are a

disease:Defects in NOTCH1 are a cause of aortic valve disease

Several transcript variants encoding different isoforms have been found for MEF2A

and a role in the stable assembly of the outer kinetochore

This protein (annexin A1) inhibits phospholipase A2 and has anti-inflammatory activity

TGFB1/TGFB

FSHR Polyclonal Antibody, 100ul[BT-AP03379] Enzyme Activity Assays disease:Defects in NOTCH1 are aFollicle 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.