
Description
Specifications
Clone | IHC564 |
Source | Mouse Monoclonal |
Positive Control | Breast |
Dilution Range | 1:200 |
E-cadherin is an intercellular adhesion molecule present in epithelial cells. Anti-E-cadherin stains glandular epithelium, as well as lung, gastrointestinal and ovarian adenocarcinomas. A panel of antibodies against E-cadherin and p120 is also used to differentiate ductal (membranous staining) and lobular breast cancer (cytoplasmic staining). Anti-E-cadherin also stains some thyroid cancers.
Clone | IHC564 |
Source | Mouse Monoclonal |
Positive Control | Breast |
Dilution Range | 1:200 |
Aspergillus niger Nucleic acid testing (NAT) is the method of choice for detection and quantification of a wide range of micro organisms. Primerdesign manufactures and supplies high quality quantitative real-time PCR kits for the detection and simultaneous quantification of numerous significant pathogens . A copy number standard curve is provided for quantification and an the internal extraction template (DNA or RNA), controls for the quality of the nucleic acid extraction and eliminates false negative results.
The kit is designed with the broadest possible detection profile to ensure that all clinically relevant strains and subtypes are detected. Target sequences are selected by working with data from key opinion leaders in the field. Multiple sequence alignments and unprecedented real-time PCR expertise in design and validation ensure the best possible kit.
Details of the target and priming specificity are included in the individual handbooks above.
Packaged, optimised and ready to use. Expect Better Data.
Exceptional value for money
Rapid detection of all clinically relevant subtypes
Positive copy number standard curve for quantification
Highly specific detection profile
High priming efficiency
Broad dynamic detection range (>6 logs)
Sensitive to < 100 copies of target
Accurate controls to confirm findings
Our SNPsig® kits use our own proprietary genotyping method to enable the identification of SARS-CoV-2 variants of concern. These products can be used on any real-time PCR machine using familiar protocols, whilst resulting in exceptional genotyping data.
Positive control templates for wild-type and variants are supplied in every kit to make data interpretation simple.
Our SNPsig® technology provides an alternative to sequencing as well as S gene target failure (SGTF) that enables scientists to analyse and monitor these specific genomic mutations. Our kits can provide a pivotal role in screening for SARS-CoV-2 variants for the purpose of genomic surveillance and studies.
For the detection of the SARS-CoV-2 variants with the 20I/501Y.V1, VOC-21FEB-02 and variants carrying the E484K mutation
Rapid detection of specific detection profiles
High priming efficiency
Sensitive to < 100 copies of target
Positive copy number standard curve for quantification
Accurate controls to confirm findings
96 reactions, includes master mix
This product is suitable for rapid extraction of DNA from tissue, cells, blood, saliva, swabs, blood spots, semen and other clinical samples. DNA can be used directly for PCR, quantitative PCR, Southern Blot, test of virus DNA and so on.
Specifications
Features | Specifications |
Main Functions | Isolation total DNA from blood, buffy coat, tissue and other samples |
Applications | Second generation sequencing, PCR, real time PCR, etc. |
Purification method | Polydisperse magnetic beads |
Purification technology | Magnetic beads technology |
Process method | Manual or automatic |
Sample type | Anticoagulant blood, concentrated blood, buffy coat, lymphocytes and cultured cells |
Sample amount | Whole blood :< 200μl; Saliva / swab:< 400μl; Tissue :< 20mg |
Yield | 0.1 – 50μg |
Elution volume | |
Time per run |
This product is based on the purification method of high binding magnetic particles. The sample is lysed and digested under the action of lysate and protease. DNA is released into the lysate. After adding magnetic particles and binding solution, DNA will be adsorbed on the surface of magnetic particles, and impurities such as proteins will be removed without adsorption. The adsorbed particles were washed with washing solution to remove proteins and impurities, washed with ethanol to remove salts, and finally DNA was eluted by Elution Buffer.
Contents | IVD3102 |
Purification Times | 200 |
MagPure Particles | 5 ml |
Proteinase K | 100 mg |
Protease Dissolve Buffer | 10 ml |
Rnase A | 40 mg |
Buffer ATL | 60 ml |
Buffer AL | 60 ml |
Buffer BD* | 20 ml |
Buffer BW1* | 110 ml |
Elution Buffer | 30 ml |
Cat.No | Reagent | IVD3102-F-96 |
Proteinase K | 50 mg | |
Protease Dissolve Buffer | 6 ml | |
RNase A | 20 mg | |
Buffer ATL | 30 ml | |
Buffer AL | 30 ml | |
96-Tip | 1 | |
Sample plate (DW Plate) | 450µl Buffer BD(Ethanol Added) | 1 |
Wash 1 Plate (DW Plate) | 600µl Buffer BW1(Ethanol Added) | 1 |
Wash 2 Plate (DW Plate) | 600µl Buffer BW1(Ethanol Added) | 1 |
Wash 3 Plate (DW Plate) | 750µl Buffer GW2, 20µl MagPure Particle | 1 |
Elution plate (DW Plate) | 80µl Elution Buffer | 1 |
Cat.No | Reagent | IVD3102-TL-06 |
Proteinase K | 50 mg | |
RNase A | 20 mg | |
Protease Dissolve Buffer | 6 ml | |
Buffer ATL | 40 ml | |
Buffer AL | 40 ml | |
AS-Tip | 12 | |
2.0ml V-bottom plate | Row 1/7:450µl Buffer BDRow 2/8:450µl Buffer BW1Row 3/9:450µl Buffer BW1Row 4/10:20μl Magpure Particle450μl Wash Buffer GW2 Row 5/11:450μl Wash Buffer GW2 Row 6/12:80µl Elution Buffer | 6 |
Storage and Stability
Proteinase K, RNase A, MagPure Particles should be stored at 2-8°C upon arrival. However, short-term storage (up to 24 weeks) at room temperature (15-25°C) does not affect their performance. The remaining kit components can be stored at room temperature (15-25°C) and are stable for at least 18 months under these conditions.
Experiment Data
This product is suitable for rapid extraction of DNA from tissue, cells, blood, saliva, swabs, blood spots, semen and other clinical samples. DNA can be used directly for PCR, quantitative PCR, Southern Blot, test of virus DNA and so on.
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Tel : 081-875-1869 , 02-328-7179
Email : hej@a3p-scientific.com
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