Peroxidasin Antikörper
-
- Target Alle Peroxidasin (PXDN) Antikörper anzeigen
- Peroxidasin (PXDN) (Peroxidasin Homolog (PXDN))
-
Reaktivität
- Human
-
Wirt
- Kaninchen
-
Klonalität
- Polyklonal
-
Konjugat
- Dieser Peroxidasin Antikörper ist unkonjugiert
-
Applikation
- Western Blotting (WB)
- Verwendungszweck
- PXDN Rabbit pAb
- Kreuzreaktivität
- Human, Maus
- Produktmerkmale
- Polyclonal Antibodies
- Aufreinigung
- Affinity purification
- Immunogen
- Recombinant protein of human PXDN.
- Isotyp
- IgG
- Top Product
- Discover our top product PXDN Primärantikörper
-
anti-Peroxidasin Homolog (PXDN) (AA 1452-1561) antibody
PXDN Reaktivität: Human WB, ELISA Wirt: Maus Monoclonal 2C11 unconjugated
anti-Peroxidasin Homolog (PXDN) (AA 76-260) antibodyPXDN Reaktivität: Human WB, IHC, IP, ICC Wirt: Kaninchen Polyclonal unconjugated
anti-Peroxidasin Homolog (PXDN) (AA 1285-1475) antibodyPXDN Reaktivität: Human WB, IHC, IP, ICC Wirt: Kaninchen Polyclonal unconjugated
anti-Peroxidasin Homolog (PXDN) (AA 1452-1561) antibodyPXDN Reaktivität: Human WB, ELISA Wirt: Maus Polyclonal unconjugated
anti-Peroxidasin Homolog (PXDN) (N-Term) antibodyPXDN Reaktivität: Human, Meerschweinchen, Pferd, Maus, Hund, Kaninchen, Ratte WB Wirt: Kaninchen Polyclonal unconjugated
-
- Applikationshinweise
- WB,1:500 - 1:2000
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
-
- 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.
-
- Target
- Peroxidasin (PXDN) (Peroxidasin Homolog (PXDN))
- Andere Bezeichnung
- PXDN (PXDN Produkte)
- Hintergrund
- This gene encodes a heme-containing peroxidase that is secreted into the extracellular matrix. It is involved in extracellular matrix formation, and may function in the physiological and pathological fibrogenic response in fibrotic kidney. Mutations in this gene cause corneal opacification and other ocular anomalies, and also microphthalmia and anterior segment dysgenesis.,PXN,VPO,MG50,PRG2,ASGD7,COPOA,D2S448,D2S448E,PXDN,Signal Transduction,Cell Biology & Developmental Biology,Cytoskeleton,Extracellular Matrix,PXDN
- Gen-ID
- 7837
- UniProt
- Q92626
-
