Cathepsin H Polyclonal Antibody, 50ul[BT-AP01240] Sampling Tubes Deficiencies lead to the skeletal

Deficiencies lead to the skeletal malformation syndrome campomelic dysplasia| frequently with sex reversal

Pseudogenes of this gene are located on chromosomes 9

after it is split into two parts

facilitated glucose transporter member 4 and other proteins

Studies in mouse show that this gene product functions as a transcription factor

Cathepsin H Polyclonal Antibody, 50ul[BT-AP01240] Sampling Tubes Deficiencies lead to the skeletalThe protein encoded by CTSH is a lysosomal cysteine proteinase important in the overall degradation of lysosomal proteins. It is composed of a dimer of disulfide linked heavy and light chains, both produced from a single protein precursor. The encoded protein (cathepsin H), which belongs to the peptidase C1 protein family, can act both as an aminopeptidase and as an endopeptidase. Increased expression of CTSH has been correlated with malignant