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Antikörper

Hbegf Polyclonal Antibody

Produktgrößen
50 ug
£302,00
CAC11350-50UG
100 ug
£454,00
CAC11350-100UG
Über dieses Produkt
SKU:
CAC11350
Zusätzliche Namen:
Diphtheria toxin receptor|diphtheria toxin receptor (heparin-binding EGF-like growth factor)|diphtheria toxin receptor (heparin-binding epidermal growth factor-like growth factor)|DT R|DT-R|DTR|DTS|DTSF|HB-EGF|HBEGF|HBEGF_HUMAN|HEGFL|Heparin binding EGF like growth factor|Heparin binding epidermal growth factor|Heparin binding epidermal growth factor like growth factor|Heparin-binding EGF-like growth factor|Proheparin binding EGF like growth factor
Anwendung:
ELISA, Immunofluorescence, Immunohistochemistry
Buffer:
0.01m PBS
CE/IVD:
RUO
translate.label.attr.clone:
Polyclonal
Klonalität:
Polyclonal
Weitere Details:
The Hbegf Polyclonal Antibody is applicable for the following applications: ELISA, IHC, IF.
Host:
Rabbit
Immunogen:
HBEGF
Isotyp:
IgG
Physischer Zustand:
Liquid
Aufreinigung:
Protein G Purified
Versandbedingungen:
Blue Ice
Quelle:
Rabbit
Lagerbedingungen:
-20[o]C Avoid freeze/thaw cycles., 2-8[o]C Avoid freeze/thaw cycles.
Hersteller:
Biomatik
Typ:
Antibody: Polyclonal Antibody
Catalog Antibody.JPG
IHC image of CAC11350 diluted at 1:100 and staining in paraffin-embedded human melanoma performed on a Leica BondTM system. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4°C overnight. The primary is detected by a biotinylated secondary antibody and visualized using an HRP conjugated SP system.
IHC image diluted at 1:100 and staining in paraffin-embedded human small intestine tissue performed on a Leica BondTM system. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4°C overnight. The primary is detected by a biotinylated secondary antibody and visualized using an HRP conjugated SP system.
Immunofluorescence staining of Hela cells with CAC11350 at 1:33, counter-stained with DAPI. The cells were fixed in 4% formaldehyde, permeabilized using 0.2% Triton X-100 and blocked in 10% normal Goat Serum. The cells were then incubated with the antibody overnight at 4°C. The secondary antibody was Alexa Fluor 488-congugated AffiniPure Goat Anti-Rabbit IgG(H+L).