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application (WB, IHC-P, IF/ICC, IP, ELISA) & cross reactivity (Human, Mouse, Rat)

application (WB, IHC-P, IP, ELISA) & cross reactivity (Human, Mouse, Rat)

application (WB, IHC-P, IP, ELISA) & cross reactivity (Human, Mouse, Rat)

application (WB, IHC-P, IP, ELISA) & cross reactivity (Human, Mouse, Rat)

application (WB, IHC-P, IP, ELISA) & cross reactivity (Human, Mouse, Rat)

application (WB, IP, IF-P, IHC-P, ELISA) & cross reactivity (Human, Mouse, Rat)

application (WB, IP, IF-P, IHC-P, ELISA) & cross reactivity (Human, Mouse, Rat)

application (WB, ELISA) & cross reactivity (Rat)

application (WB, ELISA) & cross reactivity (Rat)

AFTMag NGS DNA Clean Beads is a SPRI-based chemistry that speeds and simplifies nucleic acid size selection and PCR purification for DNA and/or RNA library preparation for Next Generation sequencing. It is compatible with mainstream NGS library prepared kits. So，it effectively reduce your library preparation costs with the same effect. The protocol can be adapted to your current liquid handling workstation (e.g. Beckman, Hamilton, Tecan, Caliper, Perkin Elmer, Agilent and Eppendorf) utilizing your current protocol as well as it can be performed manually.

AFTMag NGS DNA Clean Beads is a SPRI-based chemistry that speeds and simplifies nucleic acid size selection and PCR purification for DNA and/or RNA library preparation for Next Generation sequencing. It is compatible with mainstream NGS library prepared kits. So，it effectively reduce your library preparation costs with the same effect. The protocol can be adapted to your current liquid handling workstation (e.g. Beckman, Hamilton, Tecan, Caliper, Perkin Elmer, Agilent and Eppendorf) utilizing your current protocol as well as it can be performed manually.

This kit is a nucleic acid extraction kit based on magnetic beads, primarily designed for isolating and purifying high-quality plasmid DNA from bacteria. It utilizes the functional groups on the surface of magnetic beads to enrich nucleic acids from sample lysates onto the surface of the magnetic beads, followed by separation of the magnetic beads using a magnetic separation device to achieve rapid isolation and purification of nucleic acids. This reagent kit boasts high efficiency, speed, and convenience, and when paired with a fully automatic nucleic acid extraction instrument, it can complete the extraction of 96 samples in just approximately 25 minutes.

This kit is a nucleic acid extraction kit based on magnetic beads, primarily designed for isolating and purifying high-quality plasmid DNA from bacteria. It utilizes the functional groups on the surface of magnetic beads to enrich nucleic acids from sample lysates onto the surface of the magnetic beads, followed by separation of the magnetic beads using a magnetic separation device to achieve rapid isolation and purification of nucleic acids. This reagent kit boasts high efficiency, speed, and convenience, and when paired with a fully automatic nucleic acid extraction instrument, it can complete the extraction of 96 samples in just approximately 25 minutes. Additionally, the plasmid DNA extracted using this kit is of high purity with intact fragments, making it suitable for direct use in molecular biology experiments such as transformation, PCR amplification, sequencing, ligation, and transfection of conventional cells.

This kit is a nucleic acid extraction kit based on magnetic beads. The main principle involves using functional groups on the surface of the magnetic beads to enrich nucleic acids from the sample lysate onto the surface of the beads. The beads are then washed to remove proteins and other impurities. Then, a magnetic separation device is used to isolate the beads, allowing for rapid separation and purification of nucleic acids. The entire process does not require the use of organic reagents such as phenol, chloroform, or β-mercaptoethanol, making it safe and non-toxic. The use of paramagnetic magnetic beads is suitable for high-throughput automated extraction. The extracted product can be directly used for RT-PCR, RT-qPCR, Northern Blot, next-generation sequencing library construction, and cloning.

This kit is a nucleic acid extraction kit based on bio-nanomagnetic beads. The main principle involves using functional groups on the surface of the bio-magnetic beads to enrich nucleic acids from the sample lysate onto the surface of the beads. The beads are then washed to remove proteins and other impurities. Then, a magnetic separation device is used to isolate the beads, allowing for rapid separation and purification of nucleic acids. The entire process does not require the use of organic reagents such as phenol, chloroform, or β-mercaptoethanol, making it safe and non-toxic. The use of paramagnetic magnetic beads is suitable for high-throughput automated extraction. The extracted product can be directly used for RT-PCR, RT-qPCR, Northern Blot, next-generation sequencing library construction, and cloning.

AFTMag Quick Cell-Free DNA Extraction Maxi Kit

This kit uses magnetic bead-based technology for nucleic acid purification. It utilizes functional groups on magnetic beads to enrich nucleic acids from sample lysates onto the bead surface.The beads are then washed to remove proteins and other impurities. After that, a magnetic separation device is used to separate the magnetic beads, and then DNase I is used for digestion to remove DNA, so as to rapidly separate and purify RNA. The whole process does not require the use of phenol, chloroform and β-merphytoethanol and other harmful substances, safe and non-toxic, and the use of paramagnetic magnetic beads, suitable for high-throughput automated extraction.

This kit uses magnetic bead-based technology for nucleic acid purification. It utilizes functional groups on magnetic beads to enrich nucleic acids from sample lysates onto the bead surface.The beads are then washed to remove proteins and other impurities. After that, a magnetic separation device is used to separate the magnetic beads, and then DNase I is used for digestion to remove DNA, so as to rapidly separate and purify RNA. The whole process does not require the use of phenol, chloroform and β-merphytoethanol and other harmful substances, safe and non-toxic, and the use of paramagnetic magnetic beads, suitable for high-throughput automated extraction.

This kit uses magnetic bead-based technology for nucleic acid purification. It utilizes functional groups on magnetic beads to enrich nucleic acids from sample lysates onto the bead surface.The beads are then washed to remove proteins and other impurities. After that, a magnetic separation device is used to separate the magnetic beads, and then DNase I is used for digestion to remove DNA, so as to rapidly separate and purify RNA. The whole process does not require the use of phenol, chloroform and β-merphytoethanol and other harmful substances, safe and non-toxic, and the use of paramagnetic magnetic beads, suitable for high-throughput automated extraction.

AFTMag Quick FFPE DNA Extraction Kit

AFTMag Quick FFPE DNA Extraction Kit

AFTMag Quick FFPE DNA Extraction Kit (Prepackaged)

This kit uses magnetic bead-based technology for nucleic acid purification. It utilizes functional groups on magnetic beads to enrich nucleic acids from agarose gel onto the bead surface.The beads are then washed to remove impurities, and then separate magnetic beads with magnetic separation device, so as to quickly separate and purify DNA from samples. The whole process does not require the use of phenol, chloroform and β-merphytoethanol,, safe and non-toxic, and the use of paramagnetic magnetic beads, suitable for high-throughput automated extraction.

This kit uses magnetic bead-based technology for nucleic acid purification. It utilizes functional groups on magnetic beads to enrich nucleic acids from agarose gel onto the bead surface.The beads are then washed to remove impurities, and then separate magnetic beads with magnetic separation device, so as to quickly separate and purify DNA from samples. The whole process does not require the use of phenol, chloroform and β-merphytoethanol,, safe and non-toxic, and the use of paramagnetic magnetic beads, suitable for high-throughput automated extraction.

This kit uses magnetic bead-based technology for nucleic acid purification. It utilizes functional groups on magnetic beads to enrich nucleic acids from agarose gel onto the bead surface.The beads are then washed to remove impurities, and then separate magnetic beads with magnetic separation device, so as to quickly separate and purify DNA from samples. The whole process does not require the use of phenol, chloroform and β-merphytoethanol,, safe and non-toxic, and the use of paramagnetic magnetic beads, suitable for high-throughput automated extraction.

This kit is a nucleic acid extraction kit based on magnetic beads. The main principle involves using functional groups on the surface of the magnetic beads to enrich nucleic acids from the sample lysate onto the surface of the beads. The beads are then washed to remove proteins and other impurities. Then, a magnetic separation device is used to isolate the beads, allowing for rapid separation and purification of nucleic acids. The entire process does not require the use of organic reagents such as phenol, chloroform, or β-mercaptoethanol, making it safe and non-toxic. The use of paramagnetic magnetic beads is suitable for high-throughput automated extraction.

This kit is a nucleic acid extraction kit based on magnetic beads. The main principle involves using functional groups on the surface of the magnetic beads to enrich nucleic acids from the sample lysate onto the surface of the beads. The beads are then washed to remove proteins and other impurities. Then, a magnetic separation device is used to isolate the beads, allowing for rapid separation and purification of nucleic acids. The entire process does not require the use of organic reagents such as phenol, chloroform, or β-mercaptoethanol, making it safe and non-toxic. The use of paramagnetic magnetic beads is suitable for high-throughput automated extraction.

This kit is a nucleic acid extraction kit based on magnetic beads with high-specificity binding. The main principle involves utilizing the functional groups on the surface of the magnetic beads to enrich nucleic acids from the sample lysate onto the surface of the beads. The proteins and other impurities are removed with washing buffer, followed by separation of the beads using a magnetic separation device. DNase I digestion is then employed to remove DNA, allowing for the rapid separation and purification of RNA. The entire process does not require the use of harmful substances such as phenol, chloroform, or β-mercaptoethanol, making it safe and non-toxic. Moreover, the paramagnetic magnetic beads are suitable for high-throughput automated extraction. The extracted products can be directly used in downstream experiments such as RT-PCR, qRT-PCR, Northern Blot, next-generation sequencing library preparation, and molecular cloning.

This kit is a nucleic acid extraction kit based on magnetic beads with high-specificity binding. The main principle involves utilizing the functional groups on the surface of the magnetic beads to enrich nucleic acids from the sample lysate onto the surface of the beads. The proteins and other impurities are removed with washing buffer, followed by separation of the beads using a magnetic separation device. DNase I digestion is then employed to remove DNA, allowing for the rapid separation and purification of RNA. The entire process does not require the use of harmful substances such as phenol, chloroform, or β-mercaptoethanol, making it safe and non-toxic. Moreover, the paramagnetic magnetic beads are suitable for high-throughput automated extraction. The extracted products can be directly used in downstream experiments such as RT-PCR, qRT-PCR, Northern Blot, next-generation sequencing library preparation, and molecular cloning.

This kit is a nucleic acid extraction kit based on magnetic beads with high-specificity binding. The main principle involves utilizing the functional groups on the surface of the magnetic beads to enrich nucleic acids from the sample lysate onto the surface of the beads. The proteins and other impurities are removed with washing buffer, followed by separation of the beads using a magnetic separation device. DNase I digestion is then employed to remove DNA, allowing for the rapid separation and purification of RNA. The entire process does not require the use of harmful substances such as phenol, chloroform, or β-mercaptoethanol, making it safe and non-toxic. Moreover, the paramagnetic magnetic beads are suitable for high-throughput automated extraction. The extracted products can be directly used in downstream experiments such as RT-PCR, qRT-PCR, Northern Blot, next-generation sequencing library preparation, and molecular cloning.

This kit is a nucleic acid extraction kit based on magnetic bead separation and purification. Its main principle is to use the functional groups on the surface of functional bio – magnetic beads to enrich nucleic acids from the sample lysate onto the surface of the magnetic beads. Then, a magnetic separation device is used to separate the magnetic beads, thus enabling the rapid separation and purification of nucleic acids. During the extraction process, there is no need to use toxic phenol – chloroform extraction, nor time – consuming alcohol precipitation. This kit can be integrated with a magnetic rod method or pipetting method automatic nucleic acid extractor for high – throughput extraction experiments. It can also be manually operated using a magnetic separation rack.

This kit is a nucleic acid extraction kit based on magnetic bead separation and purification. Its main principle is to use the functional groups on the surface of functional bio – magnetic beads to enrich nucleic acids from the sample lysate onto the surface of the magnetic beads. Then, a magnetic separation device is used to separate the magnetic beads, thus enabling the rapid separation and purification of nucleic acids. During the extraction process, there is no need to use toxic phenol – chloroform extraction, nor time – consuming alcohol precipitation. This kit can be integrated with a magnetic rod method or pipetting method automatic nucleic acid extractor for high – throughput extraction experiments. It can also be manually operated using a magnetic separation rack.

This kit is a nucleic acid extraction kit based on magnetic beads. The main principle involves using functional groups on the surface of the magnetic beads to enrich nucleic acids from the sample lysate onto the surface of the beads. The beads are then washed to remove proteins and other impurities. Then, a magnetic separation device is used to isolate the beads, allowing for rapid separation and purification of nucleic acids. The entire process does not require the use of organic reagents such as phenol, chloroform, or β-mercaptoethanol, making it safe and non-toxic. The use of paramagnetic magnetic beads is suitable for high-throughput automated extraction. The extracted product can be directly used for RT-PCR, RT-qPCR, Northern Blot, next-generation sequencing library construction, and cloning.

This kit is a nucleic acid extraction kit based on magnetic beads. The main principle involves using functional groups on the surface of the magnetic beads to enrich nucleic acids from the sample lysate onto the surface of the beads. The beads are then washed to remove proteins and other impurities. Then, a magnetic separation device is used to isolate the beads, allowing for rapid separation and purification of nucleic acids. The entire process does not require the use of organic reagents such as phenol, chloroform, or β-mercaptoethanol, making it safe and non-toxic. The use of paramagnetic magnetic beads is suitable for high-throughput automated extraction. The extracted product can be directly used for RT-PCR, RT-qPCR, Northern Blot, next-generation sequencing library construction, and cloning.

This kit is a nucleic acid extraction kit based on magnetic beads. The main principle involves using functional groups on the surface of the magnetic beads to enrich nucleic acids from the sample lysate onto the surface of the beads. The beads are then washed to remove proteins and other impurities. Then, a magnetic separation device is used to isolate the beads, allowing for rapid separation and purification of nucleic acids. The entire process does not require the use of organic reagents such as phenol, chloroform, or β-mercaptoethanol, making it safe and non-toxic. The use of paramagnetic magnetic beads is suitable for high-throughput automated extraction. The extracted product can be directly used for RT-PCR, RT-qPCR, Northern Blot, next-generation sequencing library construction, and cloning.

This kit can be used for rapid extraction of RNA from various bacterial samples, and does not rely on toxic reagents such as phenol and chloroform. The unique lysis buffer rapidly lyses cells from trace samples and inactivates cell RNA enzymes. The lysate mixture passes through a gDNA Remove Column, where gDNA is removed and RNA is filtered through. After adjusting the binding conditions by ethanol, RNA is selectively bound to the silicon membrane of the adsorption column in the state of high disordered salt. In a series of rapid washing-centrifugation steps, the purified RNA is eluted from the silicon membrane with low salt RNase-free H2O. The extracted RNA can be directly used in RT-PCR, qPCR and RNA library constructing experiments.

AFTSpin Blood Fast RNA Extraction Kit

This kit is suitable for quick and simple extraction of genomic DNA from various samples inclouding blood, cells and tissue. The extracted genomic DNA fragment are large, high purity and good stability, and can be directly used in PCR, enzyme digestion and hybridization experiments. The extraction process does not require phenol-chloroform extraction. Blood, cells or tissues are lysed by lysate and digested by Proteinase K, and then can be combined with Spin Column 4 under the regulation of anhydrous ethanol. After quickly and sufficiently washing, residual impurities such as protein and salt are removed, and finally DNA is dissolved in Buffer EB2.

This kit is used for RNA extraction from complex plants (polysaccharide＆polyphenol-rich plants). The kit does not rely on toxic reagents such as phenol and chloroform, and can remove residual gDNA by silica gel column purification technology and quickly extract total plant RNA. Extracted RNA can be directly used in RT-PCR, qPCR and RNA library construction experiments.

This kit is capable of lysing cells using a modified SDS-alkaline lysis method. The crude extract is selectively bound with a unique endotoxin scavenger and centrifuged to remove the endotoxin. The silica-based membrane in the centrifugal adsorption column can bind the plasmid DNA in the solution selectively under the condition of high salt and low pH value, and then impurities and other bacterial components can be removed by the deproteinizing solution PR and washing solution WB. Finally the low-salt, high-pH eluent EB elutes pure plasmid DNA from the silica-based membrane.

This kit uses a modified SDS-alkaline lysis method to lyse cells. The special Buffer P4 and the Filtration Columns 1 can effectively remove impurities such as endotoxin, protein and other impurities.The kit is suitable for extracting plasmid DNA from 5-15 mL bacterial cultures, and the whole experimental procedure of plasmid DNA extraction could be finished within 1 h. Plasmid DNA prepared is suitable for a variety of downstream applications including restriction enzyme digestion, PCR, sequencing, ligation, transformation and cell transfection.

This kit uses a modified SDS-alkaline lysis method to lyse cells. Crude extract is selectively bound to the spin column by a unique endotoxin scavenger and centrifuged to remove endotoxin. The silicone matrix membrane in the spin column selectively binds plasmid DNA at high salt and low pH conditions, allowing for impurities and other bacterial components to be removed by Buffer PR and Buffer WB. The purified plasmid DNA is eluted from the silicone matrix membrane using low-salt and high-pH Buffer EB.

This kit can be used for rapid extraction of RNA from various trace samples, and does not rely on toxic reagents such as phenol and chloroform. The unique lysis buffer rapidly lyses cells from trace samples and inactivates cell RNA enzymes. The lysate mixture passes through a gDNA Remove Column, where gDNA is removed and RNA is filtered through. After adjusting the binding conditions by ethanol, RNA is selectively bound to the silicon membrane of the adsorption column in the state of high disordered salt. In a series of rapid washing-centrifugation steps, the purified RNA is eluted from the silicon membrane with low salt RNase-free H2O. The extracted RNA can be directly used in RT-PCR, qPCR and RNA library constructing experiments.

AFTSpin Multifunction DNA Purification Kit is capable of providing a simple and fast solution for gel recovery of DNA fragments and PCR product recovery, based on silica gel column purification technology. In the presence of high-disordering salts, the DNA fragments can be selectively adsorbed on the silica-based membrane in the spin column, and then the washing solution removes primers, nucleotides, proteins, enzymes, and other impurities through a series of rapid washing-centrifugation steps; the pure DNA is eluted from the silica-based membrane with a low-salt, high-pH elution buffer solution. Employing a unique gel lysis/binding solution formula, this kit integrates the two functions of gel lysis and binding as a whole, therefore one kit can be used in agarose DNA recovery, PCR product cleaning and purification, and enzyme digestion product purification and recovery. The gel lysis solution/binding solution is prepared as a yellow solution, which is convenient to observe the gel lysis effect and monitor the pH value change, thereby achieving the best binding effect and improving the recovery efficiency greatly.

AFTSpin Multifunction DNA Purification Kit is capable of providing a simple and fast solution for gel recovery of DNA fragments and PCR product recovery, based on silica gel column purification technology. In the presence of high-disordering salts, the DNA fragments can be selectively adsorbed on the silica-based membrane in the spin column, and then the washing solution removes primers, nucleotides, proteins, enzymes, and other impurities through a series of rapid washing-centrifugation steps; the pure DNA is eluted from the silica-based membrane with a low-salt, high-pH elution buffer solution. Employing a unique gel lysis/binding solution formula, this kit integrates the two functions of gel lysis and binding as a whole, therefore one kit can be used in agarose DNA recovery, PCR product cleaning and purification, and enzyme digestion product purification and recovery. The gel lysis solution/binding solution is prepared as a yellow solution, which is convenient to observe the gel lysis effect and monitor the pH value change, thereby achieving the best binding effect and improving the recovery efficiency greatly.

This kit employs an improved SDS-alkaline lysis method to lyse cells. The silica membrane within the spin column selectively binds plasmid DNA in the solution under high-salt and low-pH conditions. Impurities and other bacterial components are then removed using a washing buffer. Finally, pure plasmid DNA is eluted from the silica membrane using an elution buffer with low salt and high pH. This kit is suitable for extracting up to 20 μg of high-purity plasmid DNA from 1-4 mL of bacterial culture, and the extracted DNA is ready for use in various molecular biology experiments, including restriction enzyme digestion, transformation, PCR, in vitro transcription, and sequencing.

This kit employs an improved SDS-alkaline lysis method to lyse cells. The silica membrane within the spin column selectively binds plasmid DNA in the solution under high-salt and low-pH conditions. Impurities and other bacterial components are then removed using a washing buffer. Finally, pure plasmid DNA is eluted from the silica membrane using an elution buffer with low salt and high pH. This kit is suitable for extracting up to 20 μg of high-purity plasmid DNA from 1-4 mL of bacterial culture, and the extracted DNA is ready for use in various molecular biology experiments, including restriction enzyme digestion, transformation, PCR, in vitro transcription, and sequencing.

This kit is suitable for the rapid extraction of microRNA and other small RNAs from various cells and tissues. It uses a unique lysis solution to rapidly lyse cells and inactivate cellular RNases. Organic extraction is employed to remove proteins and DNA. The special silicon – based matrix membrane in the spin column can adsorb total RNA, microRNA, and other various small RNAs. Subsequently, through a series of rapid washing-centrifugation steps, cell metabolites, proteins, and other impurities are further removed. Finally, a low – salt elution buffer is used to elute pure RNA from the silicon – based matrix membrane.

This kit does not rely on toxic reagents such as phenol and chloroform, and can be used for rapid RNA extraction from common animal tissue and cell samples. The excellent silica gel column purification technology can effectively remove residual gDNA and quickly extract animal total RNA. Extracted RNA can be directly used in reverse transcription PCR, qPCR and RNA library construction experiments.

This kit is suitable for rapid and simple extraction of genomic DNA from various fresh plant tissues or cultured plant cells. The extracted genomic DNA fragments are large with high purity and stability and can be directly used for PCR, digestion, hybridization and others. The extraction process does not require phenol/chloroform extraction.