Antibody Type: Recombinant Monoclonal

Application: ELISA, WB, IHC, IF, FC

Reactivity: Human

Rabbit IgG

7X976

Human

1. Western Blot
-Positive WB detected in: L02 whole cell lysate, Hela whole cell lysate, PC-3 whole cell lysate, A549 whole cell lysate
-All lanes: EGFR antibody at 1:2000
-Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution
-Predicted band size: 135, 45, 78, 70 kDa
-Observed band size: 165 kDa
2. IHC image of TMAH-00378 diluted at 1:100 and staining in paraffin-embedded human placenta 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 Goat anti-rabbit IgG polymer labeled by HRP and visualized using 0.05% DAB.
3. Immunofluorescence staining of A549 Cells with TMAH-00378 at 1:50, counter-stained with DAPI. The cells were fixed in 4% formaldehyde, permeated by 0.2% TritonX-100, and blocked in 10% normal Goat Serum. The cells were then incubated with the antibody overnight at 4°C. Nuclear DNA was labeled in blue with DAPI. The secondary antibody was FITC-conjugated AffiniPure Goat Anti-Rabbit IgG (H+L).
4. Overlay histogram showing Jurkat cells stained with TMAH-00378 (red line) at 1:50. The cells were fixed with 70% Ethylalcohol (18h) and then incubated in 10% normal goat serum to block non-specific protein-protein interactions followedby the antibody (1µg/1*10^6 cells) for 1 h at 4°C.The secondary antibody used was FITC-conjugated goat anti-rabbit IgG (H+L) at 1/200 dilution for 30min at 4°C. Control antibody (green line) was Rabbit IgG (1µg/1*10^6 cells) used under the same conditions. Acquisition of >10,000 events was performed.

ELISA, WB, IHC, IF, FC

WB:1:500-1:5000; IHC:1:50-1:200; IF:1:20-1:200; FC:1:20-1:200.

Monoclonal

Unconjugated

A synthetic peptide: Human EGFR(ErbB 1)

Human

1956

Cancer, Signal transduction