COMP Protein (AA 22-240) (GST-His-Tag)
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- Antigène Voir toutes COMP Protéines
- COMP (Cartilage Oligomeric Matrix Protein (COMP))
- Type de proteíne
- Recombinant
- Attributs du protein
- AA 22-240
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Origine
- Humain
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Source
- Escherichia coli (E. coli)
- Purification/Conjugué
- Cette COMP protéine est marqué à la GST-His-Tag.
- Séquence
- Gly 22-His 240
- Attributs du produit
- A DNA sequence encoding the Human COMP protein (P49747) (Gly 22-His 240) was expressed with a N-GST&C-His tag.
- Pureté
- > 95 % as determined by reducing SDS-PAGE.
- Top Product
- Discover our top product COMP Protéine
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- Restrictions
- For Research Use only
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- Format
- Lyophilized
- Buffer
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Lyophilized from sterile PBS, pH 7.4.
Normally 5 % - 8 % trehalose, mannitol and 0.01 % Tween80 are added as protectants before lyophilization. - Stock
- 4 °C,-20 °C,-80 °C
- Stockage commentaire
- Generally, lyophilized proteins are stable for up to 12 months when stored at -20 to -80°C. Reconstituted protein solution can be stored at 4-8°C for 2-7 days. Aliquots of reconstituted samples are stable at < -20°C for 3 months.
- Date de péremption
- 12 months
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- Antigène
- COMP (Cartilage Oligomeric Matrix Protein (COMP))
- Autre désignation
- COMP (COMP Produits)
- Synonymes
- COMP Protein, EDM1 Protein, EPD1 Protein, MED Protein, PSACH Protein, THBS5 Protein, TSP5 Protein, cartilage oligomeric matrix protein Protein, COMP Protein, sce3551 Protein, CJA_1292 Protein, Comp Protein
- Sujet
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Abbreviation: COMP
Target Synonym: EDM1,EPD1,MED,PSACH,THBS5
Background: Cartilage Oligomeric Matrix Protein (COMP), also referred to as Thrombospondin-5, is a non-collagenous extracellular matrix (ECM) protein and belongs to the subgroup B of the thrombospondin protein family. This protein is expressed primarily in cartilage, ligament, and tendon, and binds to other ECM proteins such as collagen I, II and IX with high affinities depending on the divalent cations Zn2+ or Ni2+. COMP is a secreted glycoprotein that is important for growth plate organization and function. It is suggested to play a role in cell growth and development, and recent studies have revealed the possible mechanism that it protects cells against death by elevating members of the IAP (inhibitor of apoptosis protein) family of survival proteins. Mutations in COMP cause two skeletal dysplasias, pseudoachondroplasia (PSACH) and multiple epiphyseal dysplasia (EDM1), and up-regulated expression of COMP are observed in rheumatoid arthritis and certain carcinomas.
- Poids moléculaire
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Calculated MW: 48.98 kDa
Observed MW: 50 kDa
- UniProt
- P49747
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