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Peer Reviews from Real Labs

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BOSTER’s Ki-67 antibody can effectively mark the proliferative activity of tumor cells. After treatment, a significant decrease in Ki-67 expression in tumor tissues can be clearly observed, indicating that the proliferative activity of tumor cells is mark

Excellent, submitted by on
SKU PB9026
Application Immunofluorenscence
Sample Cells in nude mouse tumor tissue
Sample Processing Description Sections of nude mouse tumor tissues fixed and embedded under different treatment conditions (Scale Bar = 100 μm)
Primary Antibody Anti-Ki67/MKI67 Antibody Picoband®
Primary Incubation 1:200, overnight at 4 ℃
Blocking Agent Goat serum
Secondary Antibody DyLight 488-conjugated goat anti-rabbit antibody.
Secondary Incubation Incubate at room temperature for 1 hour
Detection Fluorescence microscope
Results Summary The antibodies used in the experiment demonstrated good sensitivity and high cost-effectiveness, providing strong support for the smooth progress of the study.

Accurate localization and good imaging quality

Excellent, submitted by on
SKU PB9640
Application Immunofluorenscence
Sample Mouse 4T1 cell climbing slides
Sample Processing Description Mouse 4T1 cells fixed with 4% paraformaldehyde for 15 minutes
Primary Antibody Anti-GRP78 antibody
Primary Incubation 1:400, 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 ordering and delivery cycle of the antibodies is short — I was able to receive the products within a week, which saved a lot of time. The pre-sales and after-sales services are convenient and efficient. Since my background is in chemistry, I consulted Boster’s technical staff about many details of biological experiments. The technical specialists were patient and helpful in their analysis and explanations, which allowed me to avoid many detours during the actual experimental procedures. Most importantly, these antibodies offer a high cost-performance ratio, with good binding performance, excellent imaging results, and a high experimental success rate, providing a solid foundation for conducting related experiments.

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.

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

Excellent, submitted by on
SKU A01263
Application Western Blot
Sample HEK293T
Blocking Agent 5% Non-fat milk
Primary Incubation 1:1000, overnight at 4 ℃
Secondary Antibody Anti-Rabbit IgG Secondary Antibody, HRP-conjugated
Secondary Incubation Incubate at room temperature for 1 hour
Detection Azure Biosystems c600, ECL substrate
Results Summary I will definitely purchase BosterBio products again and recommend them to my classmates and colleagues.

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.