Labcon APT™ pipette tips for Biomek® FX and NX workstations are designed to work as a plug and play solution on factory specification Biomek® units.
Available in 50µl style for 384 head pipettors. 20µl, 50µl, and 250µl style for AP96 head workstations. All APT™ tips are in a heavy reusable polypropylene SBS footprint rack. Every APT™ brand pipette tip is tinted a magenta color as your guarantee these tips will fit and work in the correct workstations.
Our APT™ tips in sterile racks, like all our other products, have received valid medical grade sterilization processing compliant with ISO 11137 to an SAL of 10-6. This is a feature you won’t get from most pipette tip suppliers, a truly sterile product. Most pipette tip makers offer only a non-validated “presterilized” product.
APT™ Automation Pipette Tips have been designed to fit Beckman® FX and NX automated pipetting workstations. They are available in 20µL, 50µL, and 250µL fluid sizes for the AP96 pipetting head and in 50µL for the AP384 pipetting head. Each size of these tips is provided in a heavy duty rack designed to accept the heavy load of automated pipette workstations. A color coded platform ensures the correct tip volume can be identfied in the Beckman® unit. APT™ tips are available in both sterile and non sterile versions. As with all Labcon products the sterile versions are sterilized using a medical grade validation to an SAL of 10-6 to ensure they can be used for diagnostic as well as research applications.
| Endotoxin Free (Non pyrogenic) Product samples are exposed to endotoxin-free water and the resulting extraction fluid is tested for contamination using the kinetic turbidimetric Limulus Amoebocyte Lysate (LAL) assay protocol and USP guidelines. All products tested must display less than 0.05 EU/ml to be certified free of endotoxin. |
| Product Name and Short Description | Thumbnails | SKU | Quantity | Total Price | Action | |
|---|---|---|---|---|---|---|
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TIP XPFL 50UL ECLIPSE MINI REFILLS Package 672 Case 5376
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8010-250-000-9
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$631.04 |
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TIP ROBOTIC 1-50UL MAGENTA for Workstations 96 Rack Package 960 Case 4800
|
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8015-690-008-9
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$785.84 |
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TIP AERO APT P50 50UL 96 Rack Sterile Package 960 Case 4800
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8124-695-000-9
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$1,006.54 |
Features
Labcon APT™ pipette tips for Biomek® FX and NX workstations are designed to work as a plug and play solution on factory specification Biomek® units.
Available in 50µl style for 384 head pipettors. 20µl, 50µl, and 250µl style for AP96 head workstations. All APT™ tips are in a heavy reusable polypropylene SBS footprint rack. Every APT™ brand pipette tip is tinted a magenta color as your guarantee these tips will fit and work in the correct workstations.
Our APT™ tips in sterile racks, like all our other products, have received valid medical grade sterilization processing compliant with ISO 11137 to an SAL of 10-6. This is a feature you won’t get from most pipette tip suppliers, a truly sterile product. Most pipette tip makers offer only a non-validated “presterilized” product.
APT™ Automation Pipette Tips have been designed to fit Beckman® FX and NX automated pipetting workstations. They are available in 20µL, 50µL, and 250µL fluid sizes for the AP96 pipetting head and in 50µL for the AP384 pipetting head. Each size of these tips is provided in a heavy duty rack designed to accept the heavy load of automated pipette workstations. A color coded platform ensures the correct tip volume can be identfied in the Beckman® unit. APT™ tips are available in both sterile and non sterile versions. As with all Labcon products the sterile versions are sterilized using a medical grade validation to an SAL of 10-6 to ensure they can be used for diagnostic as well as research applications.
| Endotoxin Free (Non pyrogenic) Product samples are exposed to endotoxin-free water and the resulting extraction fluid is tested for contamination using the kinetic turbidimetric Limulus Amoebocyte Lysate (LAL) assay protocol and USP guidelines. All products tested must display less than 0.05 EU/ml to be certified free of endotoxin. |
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| Nuclease Free (RNase/DNase) Product samples are exposed to nuclease-free water and the resulting extraction fluid is tested for nuclease activity on commercially available 7.5 kb Poly(A) tailed RNA (1µg) and HindIII-digested DNA (1µg) with a one hour 37°C incubation in appropriate buffers. Results are visualized on an agarose gel with appropriate positive and negative controls. Extraction fluid samples must show no degradation of the nucleic acids by the extraction fluid has occurred for the product to be certified as RNase-free and DNase-free |
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| Adenosine Triphosphate (ATP) Product sample surfaces are tested for the presence of adenosine triphosphate (ATP) using a controlled bioluminescence reaction to detect contamination. Luminescence data is compared to results generated by ATP-free surfaces and surfaces with known amounts of ATP as a positive control. The relative light units result must indicate less than 2 X 10-12 mg/µl of ATP for the product to be certified as ATP free. |
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| DNA Free (Human) To confirm the freedom from DNA amplification products are examined by Agarose gel electrophoresis with appropriate positive and negative controls. PCR reactions using extraction fluid must show no PCR- amplified product compared to a positive control containing one picogram of human genomic DNA for the product to be certified as DNA-free. |
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| Protease Free Product samples are tested and certified to be free of detectable Protease. Extraction fluid is tested for the presence of protease activity by examining test protein degradation in the extraction fluid compared to a negative control and positive control reactions supplemented with 2 nanograms of Proteinase K or Trypsin. |
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| Heavy Metals Free Heavy metals have been tested for using the prescribed USP method and confirmed to have levels lower than 1 part per million (1ppm) |
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| Validated Sterilization Labcon products are sterilized by radiation sterilization within a dose range of 12-35 kGy. The dose range necessary for the stated sterility assurance level is continuously audited through quarterly bio-burden and sterility validation studies performed according to the ANSI/AAMI/ISO 11137 standard by an independent laboratory. This dosage is sufficient to guarantee a sterility assurance level of 10-6. |
