Products

The qMate Mini Nucleic Acid Extraction System is designed for DNA/RNA nucleic acid extraction and purification. Leveraging magnetic bead separation technology, it precisely manipulates magnetic rods and sleeves to execute a series of procedures including sample lysis, adsorption, washing, elution, and recovery, enabling automated extraction and purification.

With a compact design, flexible processing capacity and high efficiency, it allows for immediate sample testing. Paired with Aperbio Rapid Real-time Fluorescence Quantitative PCR System, it can smoothly conduct on-the-spot sample detection across diverse outdoor settings.

Speed: 20min minutes to complete the wet transfer of 4 pieces of gels.

High compatibility: support 5-200Kda molecular weight protein.

Simple: Buffer liquid cooling circulation system, no need to bury ice.

The preparation of protein samples is crucial in Western blot experiments. High quality protein samples are the basis for accurately analyzing protein characteristics, functions, and interactions, and determine the reliability of subsequent experimental structures.

1. Fast transfer speed

2. With heat dissipation module, it can effectively dissipate heat to avoid overheating leading to experimental failure and damage to drawer electrodes

3. Flat design, support multiple stacking, save space

4. You can choose fast transfer reagent consumables or conventional reagent consumables

Substrate luminescence detection reagent is a highly sensitive enhanced chemiluminescent substrate reagent, which adopts a unique luminescent substrate system and optimizes the ingredients. The product has low background, good stability, high signal sensitivity and intensity, and long-lasting luminescence time. It is dozens of times more sensitive than ordinary ECL reagents. It is used to detect antibodies directly or indirectly labeled with horseradish peroxidase HRP and their associated antigens. It can sensitively detect the target protein.

Sometimes it is difficult to detect bands with good signals in protein Western blot detection for many reasons, including low abundance of target protein, low antibody affinity, difficult epitope identification, etc. If you encounter low signal and high background in Western blot, using the immune signal enhancement kit can significantly enhance the reaction signal and obtain ideal data faster.

1) Fully automated completion of steps such as blocking, primary antibody, secondary antibody, and cleaning in the western blot experiment process

2) Supports 12 channels, each channel can independently set programs

3) Support combinations of incubation boxes of different sizes

4) Realize temperature control of 2-40 ° C

5) Can be used for primary and secondary antibody recovery, with a recovery rate of up to 95%

6) Release human resources, avoid manual errors, and ensure higher accuracy in results

① Fast transfer: small and medium gel transfer can be completed in just 3-7 minutes

② High throughput: 1-4 small gels or 1-2 medium gels can be transferred in a single run

③ Efficient heat dissipation: Patented fluid mechanics and efficient air cooling ensure good heat dissipation and increase the service life of the drawer

④ Flexible design: Allows users to customize transfer conditions, the same as traditional semi-dry transfer consumables

⑤ Independent control: Two drawers can set transfer conditions independently, and can be used separately or simultaneously

⑥ Extra-large touch screen: Window design, clear at a glance; strong visual impact

1. Output type: constant voltage, constant current, constant power
2. Protein function: After the concentrated gel, the power supply automatically connects to theseparation gel, reducing the tediousness of manual resetting.
3. Automatic rise function: After selecting the constant value, the other two indicators automaticallynts caused by human operation.
4. Microcurrent function: Autornatically enter the microcurrent after the electrophoresis ends,avoiding the diffusion of samples with timed shutdown and preventing the samples from runningtoo far. 
5.Safety performance: overvoltage, arc, no-load and load mutation monitoring; overload/shortcircuit mitoring; leakage protection; open circuit alarm, automatic recovery from power failure,pause/lresume functior.
6. The LCD screen simultaneously displays voltage, current, power, and timing time.

① It can accommodate 1-4 hand-cast or pre-cast gels, and can complete up to 4 small gel electrophoresis within 1 hour

② The edge seal spacer is glued to the long glass plate to ensure the precise alignment of the glass plate and avoid gel leakage

③ The cam gel frame ensures precise alignment

④ It comes standard with 4 independent gel bases, which are convenient for flexible placement on narrow laboratory tables and can cast 4 gels at the same time

⑤ The comb with side teeth and built-in ridges isolates the gel from the air to avoid inhibiting the gel polymerization reaction

RIPA lysis buffer is a traditional tissue and cell rapid lysis buffer, mainly used to extract soluble proteins from animal tissues and mammalian cells, and can be used to lyse adherent cells and suspended cells. Different levels of RIPA lysis buffers, weak, medium, and strong, can be used for protein extraction according to the requirements of protein extraction. Proteins extracted with RIPA lysis buffer can be used for protein quantification, Western blot, IP, etc., and are particularly suitable for Co-IP detection.

Plant tissue protein extraction reagent can be used to extract total protein from plant samples. The plant tissue protein extracted using this reagent can be used for downstream operations such as protein activity analysis, immunoassay, protein purification, etc., and protein quantification can be performed using BCA, Bradford, and Lowry methods.