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This antibody is highly specific and efficient, suitable for detecting AKT1 protein in rat colon by Western blot, with only minor nonspecific bands.

Excellent, submitted by on
SKU M00024-1
Application Western Blot
Sample rat colon tissue
Sample Processing Description RIPA lysis buffer: Add protease inhibitor PMSF (100:1), lyse for 10 min, centrifuge at 12,000 rpm for 15 min, transfer the supernatant and mix with 5× loading buffer, denature at 100 °C for 10 min, and load onto SDS-PAGE.
Other Reagents Blocking buffer
Primary Antibody AKT1 Monoclonal Antibody
Primary Incubation 1:1000, overnight at 4 ℃
Secondary Antibody HRP Conjugated AffiniPure Goat Anti-Rabbit IgG (H+L)
Secondary Incubation 1:1000, 1 hour in room temperature
Detection Substrate: ECL, Imaging system:ChemiDoc MP
Results Summary The figure shows a schematic of Western blot results for the target protein AKT1 and the internal control Actin in rat colon across different groups. No significant differences were observed between groups; the target bands are clear and distinct, and the experimental results are satisfactory.

This antibody is highly specific and efficient, suitable for Western blot detection of AKT1 (Phospho-T450) protein in rat colon, with only minor nonspecific bands observed.

Excellent, submitted by on
SKU P00024-2
Application Western Blot
Sample rat colon tissue
Sample Processing Description RIPA lysis buffer supplemented with PMSF (100:1) was used to lyse the samples for 10 min. The lysates were centrifuged at 12,000 rpm for 15 min, and the supernatants were collected. Fivefold loading buffer was added, and the samples were denatured at 100 °C for 10 min before loading onto SDS-PAGE.
Other Reagents Blocking buffer
Primary Antibody Phospho-AKT1 (T450) Rabbit Monoclonal Antibody
Primary Incubation 1:1000, overnight at 4 ℃
Secondary Antibody HRP Conjugated AffiniPure Goat Anti-Rabbit IgG (H+L)
Secondary Incubation 1:2000, 1 hour in room temperature
Detection Substrate: ECL, Imaging system:ChemiDoc MP
Results Summary The figure shows representative Western blot results of AKT1 (Phospho-T450) and the internal control Actin in rat colon tissues from different groups. Among the low, medium, and high doses of the traditional Chinese medicine, the high-dose group exhibits the best therapeutic effect. The target bands are clear and well defined, and the experimental results are satisfactory.

This antibody is highly specific and efficient, suitable for Western blot detection of STAT3 protein in MCF-7 cells, with only minor nonspecific bands observed.

Excellent, submitted by on
SKU M00007
Application Western Blot
Sample Human mcf-7 cells
Sample Processing Description RIPA lysis buffer supplemented with a protease inhibitor cocktail was added to the cell culture dish and incubated on ice for 30 min. The lysates were then centrifuged, and the supernatants were collected. Protein concentration was determined, and samples were adjusted accordingly. Five times protein loading buffer was added, and the samples were denatured at 100 °C for 10 min. A total of 15 μL of protein sample was loaded per lane for SDS-PAGE.
Other Reagents Blocking buffer
Primary Antibody STAT3 Rabbit Monoclonal Antibody
Primary Incubation 1:500, overnight at 4 ℃
Secondary Antibody HRP Conjugated AffiniPure Goat Anti-Rabbit IgG (H+L)
Secondary Incubation 1:2000, 1 hour in room temperature
Detection Substrate: ECL, Imaging system:ChemiDoc MP
Results Summary This antibody is highly specific and efficient, suitable for Western blot detection of STAT3 protein in MCF-7 cells, with only minor nonspecific bands observed.

This antibody is highly specific and efficient, suitable for Western blot detection of ABCD3 protein in MARC-145 cells, with only minor nonspecific bands observed.

Excellent, submitted by on
SKU PA2091
Application Western Blot
Sample Monkey MARC-145 cells
Sample Processing Description RIPA lysis buffer supplemented with protease inhibitor PMSF (100:1) was used to lyse the cells for 10 min. The lysates were then centrifuged at 12,000 rpm for 15 min, and the supernatants were collected. 5× protein loading buffer was added, and samples were denatured at 100 °C for 10 min before loading onto SDS-PAGE.
Other Reagents Blocking buffer
Primary Antibody PMP70/ABCD3 Antibody Picoband®
Primary Incubation 1:1000, overnight at 4 ℃
Secondary Antibody HRP Conjugated AffiniPure Goat Anti-Rabbit IgG (H+L)
Secondary Incubation 1 hour in room temperature
Detection Substrate: ECL, Imaging system:ChemiDoc MP
Results Summary The figure shows a schematic representation of Western blot results for ABCD3 and the internal control Actin in MARC-145 cells under normal and toxin-treated conditions. The target bands are clear and well-defined, and the experimental results are satisfactory.

This antibody exhibits high specificity and efficiency and is suitable for Western blot detection of IL6 protein in MCF-7 cells, yielding clean and well-defined target bands.

Excellent, submitted by on
SKU PA1352
Application Western Blot
Sample Human mcf-7 cells
Sample Processing Description RIPA lysis buffer supplemented with a protease inhibitor cocktail was added to the cell culture dish, and the cells were lysed on ice for 30 min. The lysates were then centrifuged, and the supernatants were collected. Protein concentration was determined, and samples were adjusted to equal concentrations. Subsequently, 5× protein loading buffer was added, and the samples were denatured at 100 °C for 10 min. A total of 15 μL of protein sample was loaded per lane for SDS-PAGE electrophoresis.
Other Reagents Blocking buffer
Primary Antibody CRCP Rabbit Monoclonal Antibody
Primary Incubation 1:2000, overnight at 4 ℃
Secondary Antibody HRP Conjugated AffiniPure Goat Anti-Rabbit IgG (H+L)
Secondary Incubation 1 hour in room temperature
Detection Substrate: ECL, Imaging system:ChemiDoc MP
Results Summary As shown in the figure, the expression levels of CRCP protein in MCF-7 cells at different drug treatment time points are presented. The Western blot results obtained with this antibody are clear; although there are a few faint nonspecific bands above, they do not affect result interpretation. It can be observed that the expression of the target protein in MCF-7 cells increases with longer drug treatment times.

This antibody is highly specific and efficient, suitable for Western blot detection of Catalase protein in MARC-145 cells, with only minor nonspecific bands.

Excellent, submitted by on
SKU PB9925
Application Western Blot
Sample MARC-145 cells
Sample Processing Description Cells or tissues were lysed in RIPA buffer supplemented with protease inhibitor PMSF (100:1) for 10 minutes. The lysate was centrifuged at 12,000 rpm for 15 minutes, and the supernatant was collected. Samples were mixed with 5× loading buffer and denatured at 100 °C for 10 minutes before loading onto SDS-PAGE.
Other Reagents Blocking buffer
Primary Antibody Catalase Antibody Picoband®
Primary Incubation 1:1000, overnight at 4 ℃
Secondary Antibody Anti-rabbit IgG secondary antibody conjugated with horseradish peroxidase (HRP)
Secondary Incubation 1:10000, 1 hour in room temperature
Detection Substrate: ECL, Imaging system:ChemiDoc MP
Results Summary The figure shows a schematic representation of Western blot results for the target protein Catalase and the loading control Actin in MARC-145 cells under normal and post-infection conditions. The target bands are clear and well-defined, and the experimental results are satisfactory.

This antibody demonstrates good specificity, with minimal nonspecific bands. The target band is clear and at the correct position, and expression differences between different groups are observable.

Excellent, submitted by on
SKU M00297
Application Western Blot
Sample Mouse hippocampal tissue
Sample Processing Description An Alzheimer’s disease (AD) model was established by injecting streptozotocin (STZ) into the lateral ventricles of mice. Hippocampal tissues were collected after treatment with four different doses of QianCengTa compound, and total protein was extracted.
Other Reagents RIPA lysis buffer,Protease inhibitor,Electrophoresis buffer,Transfer buffer,Blocking buffer
Primary Antibody c-Fos Rabbit Monoclonal Antibody
Primary Incubation 1:2000, overnight at 4 ℃
Secondary Antibody HRP Goat Anti-Rabbit IgG
Secondary Incubation 1:10000, 1 hour in room temperature
Detection Substrate: ECL, Imaging system:ChemiDoc MP
Results Summary c-FOS is a marker of neuronal activation under pathological conditions. Its expression is low in normal brain tissue but elevated in the AD model, and decreases following drug treatment. Lane 1 represents normal hippocampus, lane 2 the AD model hippocampus, lanes 3, 4, and 5 correspond to increasing doses of QianCengTa compound, and lane 6 is the positive control drug. The Western blot results indicate that QianCengTa compound exhibits a therapeutic effect on AD.

The antibody has good specificity, with a clear target band at the correct position and minimal non-specific bands.

Excellent, submitted by on
SKU M00566
Application Western Blot
Sample Human A549 cells, HCC1833 cells, LU65 cells, PC-9 cells
Sample Processing Description After normal cell culture, total proteins were extracted using RIPA lysis buffer with protease inhibitors. Protein concentration was determined by BCA assay, and then the four samples were adjusted to a uniform concentration of 3 mg/mL using loading buffer.
Other Reagents RIPA lysis buffer, Protease inhibitor, Electrophoresis buffer, Transfer buffer, Blocking buffer
Primary Antibody c-Fos Rabbit Monoclonal Antibody
Primary Incubation 1:2000, overnight at 4 ℃
Secondary Antibody HRP Goat Anti-Rabbit IgG
Secondary Incubation 1:10000, 1 hour in room temperature
Detection Substrate: ECL, Imaging system:ChemiDoc MP
Results Summary The purpose of the experiment is to examine the differences in ADAM10 protein expression among different types of human lung cancer cells, in order to select suitable cells for subsequent experiments.

The antibody shows a clear target band at the correct position, and the results are good.

Excellent, submitted by on
SKU M00297
Application Western Blot
Sample Mouse hippocampal tissue
Sample Processing Description An Alzheimer’s disease (AD) model was induced by intracerebroventricular injection of streptozotocin (STZ) in mice. The mice were subsequently treated with four different doses of Qianlenta Heji, and total protein was extracted from the hippocampal tissues.
Other Reagents RIPA lysis buffer, Protease inhibitor, Electrophoresis buffer, Transfer buffer, Blocking buffer
Primary Antibody c-Fos Rabbit Monoclonal Antibody
Primary Incubation 1:2000, overnight at 4 ℃
Secondary Antibody HRP Goat Anti-Rabbit IgG
Secondary Incubation 1:10000, 1 hour in room temperature
Detection Substrate: ECL, Imaging system:ChemiDoc MP
Results Summary c-FOS serves as a marker of neuronal activation under pathological conditions. Its expression is low in normal brain tissue but elevated in AD model mice, and is reduced after treatment. In the WB assay, lane 1 corresponds to hippocampal tissue from normal mice, lane 2 to AD model mice, lanes 3–5 to hippocampi treated with increasing doses of Qianlenta Heji, and lane 6 to a positive control drug. The results demonstrate that Qianlenta Heji exhibits therapeutic effects in the AD model.

The target band of this antibody is clear and at the correct position, and it performs better than antibodies from other brands.

Excellent, submitted by on
SKU M01245
Application Western Blot
Sample Human keratinocytes isolated from skin
Sample Processing Description Keratinocytes isolated from normal skin tissue.
Other Reagents RIPA lysis buffer, Protease inhibitor, Electrophoresis buffer, Transfer buffer, Blocking buffer
Primary Antibody Albumin Rabbit Monoclonal Antibody
Primary Incubation 1:2000, overnight at 4 ℃
Secondary Antibody HRP Goat Anti-Rabbit IgG
Secondary Incubation 1:10000, 1 hour in room temperature
Detection Substrate: ECL, Imaging system:ChemiDoc MP
Results Summary Human serum albumin (ALB) is the most abundant protein in plasma, with key functions including maintaining colloid osmotic pressure, transporting substances, providing antioxidant activity, and regulating inflammation. Clinically, ALB is widely used to treat hypoalbuminemia, shock, burns, and other conditions. ALB was long thought to be secreted exclusively by hepatocytes, but recent studies suggest that other cell types may also be capable of synthesizing it. The purpose of this experiment was to verify whether human skin keratinocytes can synthesize ALB. The results show that skin keratinocytes are indeed capable of producing ALB.