Fibulin 5 Antikörper
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- Target Alle Fibulin 5 (FBLN5) Antikörper anzeigen
- Fibulin 5 (FBLN5)
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Reaktivität
- Human, Maus
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Wirt
- Kaninchen
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Klonalität
- Polyklonal
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Konjugat
- Dieser Fibulin 5 Antikörper ist unkonjugiert
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Applikation
- Western Blotting (WB), Immunofluorescence (IF)
- Produktmerkmale
- Polyclonal Antibody
- Aufreinigung
- Affinity purification
- Immunogen
- Recombinant fusion protein of human FBLN5 (NP_006320.2).
- Isotyp
- IgG
- Top Product
- Discover our top product FBLN5 Primärantikörper
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- Applikationshinweise
- WB 1:500-1:2000 IF 1:50-1:100
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Format
- Liquid
- Konzentration
- 1 mg/mL
- 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
- Fibulin 5 (FBLN5)
- Andere Bezeichnung
- FBLN5 (FBLN5 Produkte)
- Synonyme
- zgc:103575 antikoerper, FBLN5 antikoerper, MGC108414 antikoerper, Fibulin-5 antikoerper, DKFZp469K0327 antikoerper, ADCL2 antikoerper, ARCL1A antikoerper, ARMD3 antikoerper, DANCE antikoerper, EVEC antikoerper, FIBL-5 antikoerper, UP50 antikoerper, A55 antikoerper, fibulin 5 antikoerper, fbln5 antikoerper, FBLN5 antikoerper, Fbln5 antikoerper
- Hintergrund
- The protein encoded by this gene is a secreted, extracellular matrix protein containing an Arg-Gly-Asp (RGD) motif and calcium-binding EGF-like domains. It promotes adhesion of endothelial cells through interaction of integrins and the RGD motif. It is prominently expressed in developing arteries but less so in adult vessels. However, its expression is reinduced in balloon-injured vessels and atherosclerotic lesions, notably in intimal vascular smooth muscle cells and endothelial cells. Therefore, the protein encoded by this gene may play a role in vascular development and remodeling. Defects in this gene are a cause of autosomal dominant cutis laxa, autosomal recessive cutis laxa type I (CL type I), and age-related macular degeneration type 3 (ARMD3).
- Molekulargewicht
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Observed_MW: 72 kDa
Calculated_MW: 50 kDa
- Gen-ID
- 10516
- UniProt
- Q9UBX5
- Pathways
- SARS-CoV-2 Protein Interaktom
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