COMP Antikörper (AA 20-160)
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- Target Alle COMP Antikörper anzeigen
- COMP (Cartilage Oligomeric Matrix Protein (COMP))
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Bindungsspezifität
- AA 20-160
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Reaktivität
- Human
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Wirt
- Kaninchen
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Klonalität
- Polyklonal
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Konjugat
- Dieser COMP Antikörper ist unkonjugiert
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Applikation
- Western Blotting (WB), Immunofluorescence (IF)
- Sequenz
- GQGQSPLGSD LGPQMLRELQ ETNAALQDVR ELLRQQVREI TFLKNTVMEC DACGMQQSVR TGLPSVRPLL HCAPGFCFPG VACIQTESGA RCGPCPAGFT GNGSHCTDVN ECNAHPCFPR VRCINTSPGF RCEACPPGYS G
- Kreuzreaktivität
- Human, Maus, Ratte
- Produktmerkmale
- Polyclonal Antibodies
- Aufreinigung
- Affinity purification
- Immunogen
- Recombinant fusion protein containing a sequence corresponding to amino acids 20-160 of human COMP (NP_000086.2).
- Isotyp
- IgG
- Top Product
- Discover our top product COMP Primärantikörper
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- Applikationshinweise
- WB,1:500 - 1:2000,IF,1:10 - 1:100
- Kommentare
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HIGH QUALITY
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Format
- Liquid
- Buffer
- PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.
- Konservierungsmittel
- Sodium azide
- Vorsichtsmaßnahmen
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Lagerung
- -20 °C
- Informationen zur Lagerung
- Store at -20°C. Avoid freeze / thaw cycles.
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- Target
- COMP (Cartilage Oligomeric Matrix Protein (COMP))
- Andere Bezeichnung
- COMP (COMP Produkte)
- Synonyme
- COMP antikoerper, EDM1 antikoerper, EPD1 antikoerper, MED antikoerper, PSACH antikoerper, THBS5 antikoerper, TSP5 antikoerper, cartilage oligomeric matrix protein antikoerper, COMP antikoerper, sce3551 antikoerper, CJA_1292 antikoerper, Comp antikoerper
- Hintergrund
- The protein encoded by this gene is a noncollagenous extracellular matrix (ECM) protein. It consists of five identical glycoprotein subunits, each with EGF-like and calcium-binding (thrombospondin-like) domains. Oligomerization results from formation of a five-stranded coiled coil and disulfides. Binding to other ECM proteins such as collagen appears to depend on divalent cations. Contraction or expansion of a 5 aa aspartate repeat and other mutations can cause pseudochondroplasia (PSACH) and multiple epiphyseal dysplasia (MED).,COMP,EDM1,EPD1,MED,PSACH,THBS5,TSP5,Signal Transduction,Cell Biology & Developmental Biology,Cell Cycle,Cell differentiation,Cytoskeleton,Extracellular Matrix,Bone,Stem Cells,Mesenchymal Stem Cells,COMP
- Molekulargewicht
- 77 kDa/82 kDa
- Gen-ID
- 1311
- UniProt
- P49747
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