COLGALT1 Rabbit Polyclonal Antibody, 20ul Filtration Knockout mouse studies show defects

Knockout mouse studies show defects in the formation of vertebrae and ribs that also involve cartilage formation in these structures

Take risks with our 1000 mL Sterile Vacuum Upper Cup

Mutations in this gene have been implicated in autosomal dominant Alzheimer disease and cerebroarterial amyloidosis (cerebral amyloid angiopathy)

defects in processing chondrocalcin

CSRNP3 (Cysteine And Serine Rich Nuclear Protein 3) is a Protein Coding gene

COLGALT1 Rabbit Polyclonal Antibody, 20ul Filtration Knockout mouse studies show defectsThe protein encoded by this gene is one of two enzymes that transfers galactose moieties to hydroxylysine residues of collagen and mannose binding lectin. This gene is constitutively expressed and encodes a soluble protein that localizes to the endoplasmic reticulum.