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Antibodies

Edar Polyclonal Antibody

Product Sizes
50 ug
£302.00
CAC11273-50UG
100 ug
£454.00
CAC11273-100UG
About this Product
SKU:
CAC11273
Additional Names:
Anhidrotic ectodysplasin receptor 1|DL|Downless (mouse) homolog|Downless homolog|Downless mouse homolog of|ECTD10A|ECTD10B|Ectodermal dysplasia receptor|Ectodysplasin 1 anhidrotic receptor|Ectodysplasin A receptor|Ectodysplasin A1 isoform receptor|Ectodysplasin-A receptor|ED 1R|ED 3|ED 5|ED1R|ED3|ED5|EDA 1R|EDA 3|EDA A1 receptor|EDA A1R|EDA-A1 receptor|EDA1R|EDA3|Edar|EDAR_HUMAN|HRM1|Tumor necrosis factor receptor superfamily member EDAR
Application:
ELISA, Immunofluorescence, Immunohistochemistry, Western Blot
Buffer:
0.01m PBS
CE/IVD:
RUO
translate.label.attr.clone:
Polyclonal
Clonality:
Polyclonal
Extra Details:
The Edar Polyclonal Antibody is applicable for the following applications: ELISA, WB, IHC, IF.
Host:
Rabbit
Immunogen:
EDAR
Isotype:
IgG
Physical State:
Liquid
Purification:
Protein G Purified
Shipping Conditions:
Blue Ice
Source:
Rabbit
Storage Conditions:
-20[o]C Avoid freeze/thaw cycles., 2-8[o]C Avoid freeze/thaw cycles.
Supplier:
Biomatik
Type:
Antibody: Polyclonal Antibody
Catalog Antibody.JPG
Western Blot; Positive WB detected in: A549 whole cell lysate; All lanes: EDAR antibody at 2.7ug/ml; Secondary; Goat polyclonal to rabbit IgG at 1/50000 dilution; Predicted band size: 49, 52 kDa; Observed band size: 49 kDa
IHC image diluted at 1:500 and staining in paraffin-embedded human liver cancer 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 1:500 and staining in paraffin-embedded human bladder cancer 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 MCF-7 cells with CAC11273 at 1:166, 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).