This is a synthetic peptide designed for use in combination with anti-COL9A1 Antibody. It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.
Aufreinigung
Purified
Applikationshinweise
Each Investigator should determine their own optimal working dilution for specific applications.
Beschränkungen
Nur für Forschungszwecke einsetzbar
Format
Lyophilized
Rekonstitution
Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
Konzentration
1 mg/mL
Buffer
Final peptide concentration is 1 mg/mL in PBS.
Handhabung
Avoid repeated freeze-thaw cycles.
Lagerung
-20 °C
Informationen zur Lagerung
For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
Target
COL9A1
(Collagen, Type IX, alpha 1 (COL9A1))
Synonyme
cb339 Peptide, sb:cb339 Peptide, zgc:85892 Peptide, wu:fa12a12 Peptide, wu:fa12d02 Peptide, wu:fc22c08 Peptide, wu:fc38d08 Peptide, edm6 Peptide, MGC82441 Peptide, DJ149L1.1.2 Peptide, EDM6 Peptide, MED Peptide, STL4 Peptide, Col9a-1 Peptide, collagen, type IX, alpha 1b Peptide, collagen, type IX, alpha 1 L homeolog Peptide, collagen type IX alpha 1 chain Peptide, collagen, type IX, alpha 1 Peptide, collagen alpha-1(IX) chain Peptide, col9a1b Peptide, col9a1.L Peptide, COL9A1 Peptide, Col9a1 Peptide, LOC101102992 Peptide
Hintergrund
This gene encodes one of the three alpha chains of type IX collagen, which is a minor (5-20 % ) collagen component of hyaline cartilage. Type IX collagen is usually found in tissues containing type II collagen, a fibrillar collagen. Studies in knockout mice have shown that synthesis of the alpha 1 chain is essential for assembly of type IX collagen molecules, a heterotrimeric molecule, and that lack of type IX collagen is associated with early onset osteoarthritis. Mutations in this gene are associated with osteoarthritis in humans, with multiple epiphyseal dysplasia, 6, a form of chondrodysplasia, and with Stickler syndrome, a disease characterized by ophthalmic, orofacial, articular, and auditory defects. Two transcript variants that encode different isoforms have been identified for this gene.
Alias Symbols: DJ149L1.1.2, EDM6, FLJ40263, MED, STL4