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Results for Assays & Kits ( 14531 )

    • From: £2,880.00

      The RayBio® Mouse Absolute Mitochondrial DNA Copy Number Quantification Kit is a Taqman® probe-based qPCR assay for the specific quantitative measurement of Mouse mtDNA copy number (mtDNA-CN).

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    • From: £692.00

      The RayBio® Mouse Mitochondrial DNA Damage Quantification Kit is a Taqman® probe-based qPCR assay for the specific quantitative measurement of Mouse mtDNA damage.

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    • From: £2,880.00

      The RayBio® Mouse Mitochondrial DNA Damage Quantification Kit is a Taqman® probe-based qPCR assay for the specific quantitative measurement of Mouse mtDNA damage.

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    • Ref: LL01-10
      Sizes: 1 set
      From: £153.00

      All-in-one kit for making phase-separated droplets with BSA (Bovine Serum Albumin), Droplets are easy to observe using only a micropipette and microscope, Includes a user's manual with calculation examples and details on how to use it

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    • Ref: LL02-10
      Sizes: 300 tests
      From: £359.00

      Set of reagents necessary to confirm the conditions for making phase-separated droplets, Crowding agent, pH, and salt can be optimized with this kit, Includes user's manual with sample calculations and methods for adjusting buffer pH

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    • From: £342.00

      Detect SA-β-Gal levels, Compatible with co-staining with immunostaining, Enable multiple staining with common green and red dyes

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    • Ref: N025
      Sizes: 1000 assays
      From: £274.00

      The iQuant™ microRNA Assay Kit is ideal for quantification of small RNA, including microRNA and siRNA, and both single stranded and double stranded RNA. The assay kit is highly selective for small RNA over rRNA or large mRNA. The assay kit offers advantages in stability, linear dynamic range, and sensitivity over other traditional of RNA quantitation. The assay kit contains concentrated quantitation reagent, dilution buffer, and pre-diluted microRNA standards. Simply dilute the reagent using the buffer provided, add your sample (any volume between 1 µl and 20 µl is acceptable), and read the fluorescence using fluorescence plate reader or Fluorometer (Figure 1). The assay is well tolerated to common contaminants such as proteins, salts, solvents, detergents, or free nucleotides. The assay can be adapted for use in microplates, tubes or cuvettes.

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    • From: £1,157.00

      The TR-FRET In vitro E3 activity kit has been developed to be simple, fast, and easy to use while being robust and sensitive. As E3 ligases autoubiquitinate they build long polyubiquitin chains; our unique assay will detect these chains as they are being built. This assay is homogenous and compatible for High-throughput Screening (HTS). Choose 1 E2 option among: UBE2D3 (UbcH5c), UBE2L3 (UbcH7), UBE2K (UbcH1), Ubc13, Mms2 (yeast), UBE2D2 (UbcH5b, E2-17K2), UBE2R1 (CDC34), UBE2R2 (Ubc3B), Non-tagged UBE2D1, His6-SUMO tagged UBE2D1, UBE2E2 (UbcH8), UBE2E3 (UbcH9), His6-tagged UBE2H (E2-20K), His6-SUMO tagged UBE2H (E2-20K), UBE2F (NCE2), UBE2M (Ubc12), UBE2N (Ubc13), Non-tagged UBE2T (PIG50), His6-SUMO tagged UBE2T (PIG50), UBE2V2 (MMS2, UEV-2), UBE2S (E2EPF), UBE2C (Ubc10), His6-tagged UBE2W (Ubc 16), UBE2Q2, His6-tagged UBE2A, Non-tagged UBE2G2 (Ubc7), His6-SUMO tagged UBE2G2 (Ubc7), His6-tagged UBE2I (Ubc9), UBE2L6 (UbcH8), UBE2Z (Use1) And Choose 1 E3 option among: ITCH, Traf6, GP78,

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    • From: £987.00

      The Fc (IgG1): FcRn Inhibitor Screening Colorimetric Assay Kit is designed for the screening and profiling of neutralizing antibodies or inhibitors of the interaction between human Fc (IgG1) and human FcRn (Neonatal Fc receptor for IgG). This kit comes in a convenient 96-well or 384-well format, with purified Biotinylated-FcRn complex (Fc receptor amino acids 24-297 and B2M amino acids 21-119) and Fc (IgG1) (amino acids 100-330) proteins, Streptavidin-HRP, and assay buffers for 100 or 400 reactions. A 96-well plate is coated with Fc (IgG1) protein. After blocking, the plate is pre-incubated with an inhibitor or neutralizing antibody. Upon subsequent incubation with FcRn-biotin, the plate is treated with Streptavidin-HRP followed by addition of a colorimetric HRP substrate to produce color, which can be quenched and measured using a UV/Vis microplate reader. The signal is proportional to the binding of FcRn to Fc (IgG1).

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