TXNRD1 Recombinant Monoclonal Antibody, Cat#RAC08237
Western Blot, Positive WB detected in: K562 whole cell lysate (30ug), JURKAT whole cell lysate (30ug),MCF-7 whole cell lysate (30ug),Hela whole cell lysate (30ug),COLO-205 whole cell lysate (30ug),A549 whole cell lysate (20ug),HepG2 whole cell lysate (30ug), All lanes: TR antibody at 1:1000, Secondary, Goat polyclonal to rabbit IgG at 1/40000 dilution, Predicted band size: 71 kDa, Observed band size: 57 kDa, Exposure time:2min
Immunofluorescence staining of HepG2 cell with RAC08237 at 1:50, 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).
Overlay Peak curve showing Hela cells stained with RAC08237 (red line) at 1:100. The cells were fixed in 4% formaldehyde and permeated by 0.2% TritonX-100 for 10min. Then 10% normal goat serum to block non-specific protein-protein interactions followed by the antibody (1ug/1*10_6cells) for 45min at 4℃. The secondary antibody used was FITC-conjugated goat anti-rabbit IgG (H+L) at 1/200 dilution for 35min at 4℃.Control antibody (green line) was Rabbit IgG (1ug/1*10_6cells) used under the same conditions. Acquisition of >10,000 events was performed.
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TXNRD1 Recombinant Monoclonal Antibody, Cat#RAC08237 Western Blot, Positive WB detected in: K562 whole cell lysate (30ug), JURKAT whole cell lysate (30ug),MCF-7 whole cell lysate (30ug),Hela whole cell lysate (30ug),COLO-205 whole cell lysate (30ug),A549 whole cell lysate (20ug),HepG2 whole cell lysate (30ug), All lanes: TR antibody at 1:1000, Secondary, Goat polyclonal to rabbit IgG at 1/40000 dilution, Predicted band size: 71 kDa, Observed band size: 57 kDa, Exposure time:2min Immunofluorescence staining of HepG2 cell with RAC08237 at 1:50, 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). Overlay Peak curve showing Hela cells stained with RAC08237 (red line) at 1:100. The cells were fixed in 4% formaldehyde and permeated by 0.2% TritonX-100 for 10min. Then 10% normal goat serum to block non-specific protein-protein interactions followed by the antibody (1ug/1*10_6cells) for 45min at 4℃. The secondary antibody used was FITC-conjugated goat anti-rabbit IgG (H+L) at 1/200 dilution for 35min at 4℃.Control antibody (green line) was Rabbit IgG (1ug/1*10_6cells) used under the same conditions. Acquisition of >10,000 events was performed.

TXNRD1 Recombinant Monoclonal Antibody

BiomatikSKU: RAC08237-100ul
Size: 100ul
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Western Blot, Positive WB detected in: K562 whole cell lysate (30ug), JURKAT whole cell lysate (30ug),MCF-7 whole cell lysate (30ug),Hela whole cell lysate (30ug),COLO-205 whole cell lysate (30ug),A549 whole cell lysate (20ug),HepG2 whole cell lysate (30ug), All lanes: TR antibody at 1:1000, Secondary, Goat polyclonal to rabbit IgG at 1/40000 dilution, Predicted band size: 71 kDa, Observed band size: 57 kDa, Exposure time:2min
Immunofluorescence staining of HepG2 cell with RAC08237 at 1:50, 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).
Overlay Peak curve showing Hela cells stained with RAC08237 (red line) at 1:100. The cells were fixed in 4% formaldehyde and permeated by 0.2% TritonX-100 for 10min. Then 10% normal goat serum to block non-specific protein-protein interactions followed by the antibody (1ug/1*10_6cells) for 45min at 4℃. The secondary antibody used was FITC-conjugated goat anti-rabbit IgG (H+L) at 1/200 dilution for 35min at 4℃.Control antibody (green line) was Rabbit IgG (1ug/1*10_6cells) used under the same conditions. Acquisition of >10,000 events was performed.

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We got help from Biomatik for our studies, and the experience was excellent. The customer support team was responsive and knowledgeable, providing detailed documentation and timely updates throughout the process. We appreciate the reliable quality and professional service, and we look forward to working with Biomatik again for further.

Keyao Yu

I work on molecular farming, producing recombinant protein in plant suspention cells. I'm completely satisfied after almost 5 years ordering antibidies at Biomatik. Perfect reproducibility batch after batch and I hope to continiue like this!

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The peptide product is of exceptional quality and is highly recommended for its efficacy.

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I have been using Biomatik's modified peptides for a while and they deliver high quality peptides and a very good technical support

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I have bought peptides from Biomatic several times and the quality is the best!!!

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