gb StarTaq PCR Mix gb StarTaq PCR Mix is intended for PCR and real-time PCR analysis using fluorescently labelled probes. It is suitable for applications requiring high sensitivity and amplification efficiency. One of its key advantages is its increased resistance to PCR inhibitors.
gb StarTaq IPC PCR Mix gb StarTaq IPC PCR Mix is intended for real-time PCR applications using fluorescently labelled probes. It is suitable for applications requiring high sensitivity and amplification efficiency. Its advantages include the presence of an internal positive control, as well as increased resistance to PCR inhibitors.
gb StarUDG PCR Mix gb StarUDG PCR Mix is intended for PCR and real-time PCR analysis using fluorescently labelled probes. It enables highly sensitive detection of template DNA. The PCR Mix contains uracil-DNA glycosylase (UDG), which reduces the risk of cross-contamination and primer-dimerization.
gb Ideal PCR Master Mix gb Ideal PCR Master Mix consists of hot-start Taq DNA polymerase, reaction buffer, dNTP and MgCl2. Taq polymerase is chemically modified DNA polymerase from Thermus aquaticus. This polymerase is completely inactive at room temperature but it is rapidly activated during the initial denaturation step of PCR. The product falls into a group of TaqMan Real-Time PCR Master Mixes to provide probe-based qPCR.
gb Elite PCR Master Mix gb Elite PCR Master Mix falls into a group of TaqMan Real-Time PCR Master Mixes to provide probe-based qPCR. The product consists of hot-start Taq DNA polymerase, reaction buffer, dNTP, MgCl2 and additives that prevent PCR inhibition. Taq polymerase is chemically modified DNA polymerase from Thermus aquaticus. This polymerase is completely inactive at room temperature but it is rapidly activated during the initial denaturation step of PCR.
gb IPC PCR Master Mix gb IPC PCR Master Mix falls into a group of TaqMan Real-Time PCR Master Mixes to provide probe-based qPCR. The product consists of hot-start Taq DNA polymerase, reaction buffer, dNTP, MgCl2 and additives that prevent PCR inhibition and Internal positive control (IPC). IPC included in the Master Mix serves to verify that the PCR procedure was done properly.
gb SG PCR Master Mix gb SG PCR Master Mix falls into a group of Real-Time PCR Master Mixes to provide Dye-based qPCR. The product consists of hot-start Taq DNA polymerase, reaction buffer, dNTP, MgCl2, sybrgreen and additives that prevent PCR inhibition. Taq polymerase is chemically modified DNA polymerase from Thermus aquaticus. This polymerase is completely inactive at room temperature but it is rapidly activated during the initial denaturation step of PCR.
gb StarGreen PCR Mix gb StarGreen PCR Mix is intended for real-time PCR analysis using SYBR Green instead of fluorescently labelled probe. gb StarGreen PCR Mix can also be used for the end-point PCR analysis. Beneficial feature is enhanced resistance to PCR inhibitors.
Passive reference dye Passive reference dye is an inert dye which serves as inner reference dye for fluorescence signal normalization between the wells which can occur as a result of errors in pipetting or under the influence of device limitations. It is used with TaqMan Real-Time PCR Master Mixes to provide probe-based qPCR or with probe-based One-Step qRT-PCR.
gb OneStep RT-qPCR Kit gb OneStep RT-qPCR Kit falls into a group of TaqMan Real-Time PCR Master Mixes. It provides cDNA synthesis in one-step. The product is intended for reverse transcription (RT) and real-time PCR (qPCR) performed in one step (in one reaction), i.e. onestep RT-qPCR. No additional instrumentation is required.
gb OneStep IPC Elite RT-qPCR Kit gb OneStep IPC Elite RT-qPCR Kit falls into a group of TaqMan Real-Time PCR Master Mixes. It provides cDNA synthesis and qPCR in one-step. The product is intended for high sensitivity reverse transcription (RT) and real-time PCR (qPCR) performed in one step (in one reaction), i.e. onestep RT-qPCR. No additional instrumentation is required. The kit contains IPC.
gb Elite Reverse Transcription Kit gb Elite Reverse Transcription Kit is intended for reverse transcription using enzyme MMLV reverse transcriptase. This enzyme converts RNA to cDNA (complementary DNA) in one step (without denaturation), you only have to add your template RNA.
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