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Accurate localization and good imaging quality

Excellent, submitted by on
SKU PA1239
Application Immunofluorenscence
Sample Rat Brain
Sample Processing Description Fixed in 4% paraformaldehyde for 48 hours, followed by paraffin embedding and sectioning.
Primary Antibody Anti-GFAP antibody
Primary Incubation 1:500, overnight at 4 ℃
Blocking Agent Goat serum
Secondary Antibody DyLight 550-conjugated goat anti-rabbit antibody.
Secondary Incubation Incubate at room temperature for 1 hour
Detection Laser confocal microscopy
Results Summary During the experiment, this primary antibody can be conveniently used with the complimentary antibody diluent provided. The results obtained showed good quality and reproducibility, with no false-positive signals. Overall, this primary antibody offers excellent cost performance and provides key data and strong support for publication.

This antibody exhibits high specificity, an excellent signal-to-noise ratio, and clear, stable staining, and has been successfully applied in immunofluorescent labeling of mouse cartilage tissue.

Excellent, submitted by on
SKU PA2141-1
Application Immunofluorescence
Sample mouse cartilage tissue
Sample Processing Description Freshly dissected bone samples were first fixed overnight in 4% paraformaldehyde (PFA), followed by decalcification for 3 days in 10% ethylenediaminetetraacetic acid (EDTA) solution, and then dehydrated for 1 day in 30% sucrose solution. The bone samples were subsequently embedded in optimal cutting temperature compound (OCT; Sakura, Cat. No. OCT-4583) and cryosectioned at a thickness of 10 μm using a Leica CryoJane cryostat.
Primary Antibody Anti-Collagen II/COL2A1 Antibody Picoband®
Primary Incubation 1:100, overnight at 4 °C.
Secondary Antibody donkey anti-rabbit Alexa Fluor 555 Secondary Antibody
Secondary Incubation 1:500, Incubate at room temperature for 1 hour
Other Reagents used PBS with 10% horse serum, DAPI
Detection fluorescence microscope (Leica)
Results Summary I will purchase BosterBio products again and recommend them to my classmates and colleagues.

Accurate localization and good imaging performance.

Excellent, submitted by on
SKU PB9093
Application Immunofluorenscence
Sample Mouse 4T1 cell xenograft tumor
Sample Processing Description Fixed in 4% paraformaldehyde for 48 hours, followed by paraffin embedding and sectioning.
Primary Incubation 1:200, overnight at 4 ℃
Blocking Agent Goat serum
Secondary Antibody DyLight 550-conjugated goat anti-rabbit antibody.
Secondary Incubation Incubate at room temperature for 1 hour
Detection Laser confocal microscopy
Results Summary The delivery time for antibodies is impressively fast — I usually receive the products within a week, which saves me a lot of valuable time. Both the pre-sales and after-sales support are efficient and reliable. Since my background is in chemistry, I often consulted Boster’s technical specialists about various details of biological experiments. They were always patient and thorough in their explanations, helping me avoid many detours during my experiments. Most importantly, these antibodies offer excellent value for money — they have strong binding performance, produce clear imaging results, and ensure a high experiment success rate, which has provided a solid foundation for my research.

In this study, this antibody was mainly used for Western Blot experiments. In the Western Blot results, the CCT3 antibody showed a clear and specific target band and maintained a strong signal even after multiple rounds of reuse.

Excellent, submitted by on
SKU PB9926
Application Western Blot
Sample U2OS cells
Primary Incubation 1:1000
Blocking Agent BSA
Secondary Antibody Anti-Rabbit IgG Secondary Antibody, HRP-conjugated
Results Summary I will definitely purchase BosterBio products again and recommend them to my classmates and colleagues.

The antibody is highly efficient and specific, showing a clear target band with no non-specific bands.

Excellent, submitted by on
SKU M30929
Application Western Blot
Sample HEK293T
Primary Incubation 1:1000, overnight at 4 ℃
Blocking Agent 5% non-fat milk
Secondary Antibody Anti-Rabbit IgG Secondary Antibody, HRP-conjugated
Secondary Incubation Incubate at room temperature for 1 hour
Detection Signal was developed using ECL substrate on a Azure Biosystems c600.
Results Summary I will definitely purchase BosterBio products again and recommend them to my classmates and colleagues.

Thank you for all the work on this project

Excellent, submitted by on
SKU DZ01481
Application Immunofluorescence
Sample wildtype and KO mutant zebrafish retina
Primary Incubation 1:200
Blocking Agent 10% normal goat serum and 2% bovine serum albumin in PBS
Secondary Antibody Alexa Fluor 568 goat anti-rabbit was used in blocking solution.

This antibody shows excellent consistency and reproducibility across batches, ensuring reliable and stable experimental results. Its performance remains consistent across different experiments, providing strong technical support for our research.

Excellent, submitted by on
PA1079 wb
SKU PA1079
Application Western Blot
Sample Mouse lung tissue
Sample Processing Description Tissue samples were directly lysed in RIPA buffer, mixed with loading buffer at the appropriate ratio, and denatured by heating at 98 °C. Load 20 µL of protein sample per lane onto SDS-PAGE.
Primary Incubation The membrane was incubated with TNF-α primary antibodies (1:1000) overnight at 4 °C.
Secondary Antibody HRP-conjugated Goat Anti-Rabbit IgG Secondary Antibody
Secondary Incubation Incubate at room temperature for 1 hour
Other Reagents used 5% Non-fat milk
Detection Signal was developed using ECL substrate on an ChemiDoc MP system.
Results Summary This antibody shows excellent consistency and reproducibility across batches, ensuring reliable and stable experimental results. Its performance remains consistent across different experiments, providing strong technical support for our research.

This antibody shows excellent consistency and reproducibility across batches, ensuring reliable and stable experimental results. Its performance remains consistent across different experiments, providing strong technical support for our research.

Excellent, submitted by on
SKU M03918
Application Western Blot
Sample Mouse brown adipose tissue
Sample Processing Description Tissue and cell proteins were extracted using RIPA buffer. After BCA quantification, 5× loading buffer was added, and the samples were boiled for 5 minutes for denaturation.
Primary Incubation The membrane was incubated with the PLIN1 primary antibodies (1:1000) overnight at 4 °C.
Secondary Antibody Goat Anti-Rabbit IgG Antibody (1:5000)
Secondary Incubation Incubate at room temperature for 1 hour
Other Reagents used Non-fat milk
Detection Signal was developed using ECL substrate
Results Summary This antibody shows excellent consistency and reproducibility across batches, ensuring reliable and stable experimental results. Its performance remains consistent across different experiments, providing strong technical support for our research.

The antibody is highly efficient and specific, showing a clear target band with no nonspecific bands.

Excellent, submitted by on
SKU M00220-1
Application Western Blot
Sample Mouse lung cancer tissue
Sample Processing Description Tissue samples were directly lysed in RIPA buffer, mixed with loading buffer at the appropriate ratio, and denatured by heating at 98 °C. Load 20 µL of protein sample per lane onto SDS-PAGE.
Primary Incubation The membrane was incubated with the CD86 primary antibodies (1:2000) overnight at 4 °C.
Secondary Antibody HRP-conjugated Goat Anti-Rabbit IgG Secondary Antibody
Secondary Incubation Incubate at room temperature for 1 hour
Other Reagents used 5% non-fat milk
Detection Signal was developed using ECL substrate on an Tanon system.
Results Summary The antibody is highly efficient and specific, showing a clear target band with no nonspecific bands. I will definitely continue using BosterBio products and will recommend them to my classmates and colleagues.

IL-6 and IL-1β levels in the pancreas are key for assessing the anti-inflammatory effect of this nanomedicine. Antibodies from two previous suppliers showed poor specificity, while BosterBio antibodies proved highly specific, potent, and cost-effective.

Excellent, submitted by on
SKU M00101-1
Application Western Blot
Sample Mouse pancreatic acinar cells
Sample Processing Description After centrifugation, collect the supernatant. Take a small portion for protein quantification using the BCA assay. Mix the remaining protein solution with an equal volume of loading buffer and denature in a 100°C water bath for 5 mins.
Primary Incubation The membrane was incubated with the IL-6 and IL-1β primary antibodies (1:1000) overnight at 4 °C.
Secondary Antibody HRP-conjugated Goat Anti-Rabbit IgG Secondary Antibody
Secondary Incubation Incubate at room temperature for 1 hour
Other Reagents used Protein-Free Blocking Buffer
Detection Signal was developed using ECL substrate on a ChemiDoc MP system.
Results Summary IL-6 and IL-1β levels in the pancreas are key for assessing the anti-inflammatory effect of this nanomedicine. Antibodies from two previous suppliers showed poor specificity, while BosterBio antibodies proved highly specific, potent, and cost-effective. In our subsequent experiments, our group continued to use BosterBio products, which proved to be highly reliable and provided solid support for the publication of several articles.