The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
Protein concentration is above or equal to 0.05 mg/ml.
Concentration information loading...
Preparation and Storage
Stability and Storage
Shipped on dry ice. Upon delivery aliquot and store at -80ºC. Avoid freeze / thaw cycles.
pH: 8.00 Constituents: 0.31% Glutathione, 0.79% Tris HCl
Alpha 1 type V collagen
Alpha 2 type V collagen
Collagen alpha 1(V) chain
Collagen alpha 2 (V) chain precursor
Collagen alpha 2(V) chain
Collagen alpha 3(V) chain
Collagen alpha-1(V) chain
Collagen fetal membrane A polypeptide
Collagen type V alpha 1
Collagen type V alpha 2
Collagen type V alpha 3
Collagen V alpha 2 polypeptide
Pro alpha 1 type V collagen
Pro alpha 3(V) collagen
Procollagen alpha 2(V)
Type V preprocollagen alpha 2 chain
Type V collagen is a member of group I collagen (fibrillar forming collagen). It is a minor connective tissue component of nearly ubiquitous distribution. Type V collagen binds to DNA, heparan sulfate, thrombospondin, heparin, and insulin.
Involvement in disease
Ehlers-Danlos syndrome 1 Ehlers-Danlos syndrome 2
Belongs to the fibrillar collagen family. Contains 1 fibrillar collagen NC1 domain. Contains 1 laminin G-like domain.
The C-terminal propeptide, also known as COLFI domain, have crucial roles in tissue growth and repair by controlling both the intracellular assembly of procollagen molecules and the extracellular assembly of collagen fibrils. It binds a calcium ion which is essential for its function.
Prolines at the third position of the tripeptide repeating unit (G-X-Y) are hydroxylated in some or all of the chains. Sulfated on 40% of tyrosines.
Secreted > extracellular space > extracellular matrix.