Portable 4000rpm TD4C Centrifuge Machine for Lab, PRP & PRF
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Portable 4000rpm TD4C Centrifuge Machine for Lab, PRP & PRF
Application:
Widely used in the laboratory, hospital, clinic and so on.
Product Features:
1. Brushless motor, free maintenance, no powder pollution, quick in speed up and down.
2. Rang of speed from 0~4000rpm, smooth in operation, low noise and small vibration.
3. Micro-computer control system, digital display the RCF, time and speed.
4. Electric cover lock, compact design, super speed and imblance protection.
5. Small and portable, very convenient to use.
Technical Parameters:
Max. Speed
4000rpm
Speed Accuracy
±20rpm
Max.Volume
8x20ml
Acc/Dec
10 Kinds
Max. RCF
1880xg
Power Supply
AC110V/220V 50HZ/60HZ
Timer
0~99min
Noise
≤55dBA
Dimension
310x270x220mm
Net Weight
6.5Kg
Warranty
1 Year
Certifications
CE, ISO & Calibration report are available.
Matched Rotors:
Order No.
Rotor Type
Max.Speed(rpm)
Max.Volume(ml)
Max.RCF(xg)
4C-1
Angle Rotor
4000
8x15ml/20ml
1800/1840
4C-2
Angle Rotor
4000
6x10ml/15ml/20ml
1790
4C-3
Angle Rotor
4000
12x5ml
1540
4C-4
Angle Rotor
4000
12x10ml/7ml
1792
4C-5
Angle Rotor
4000
8x10ml vacuum tube
1790
8x5ml vacuum tube adapter
1790
8x7ml vacuum tube adapter
1790
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D5001 MagPure Gel Pure DNA Kit
Product Info
Document
Product Info
Introduction
A highly efficient, easily automated agarose gel or PCR purification system that delivers superior quality DNA with no salt carryover. Requiring no centrifugation or filtration. The Kit can be easily used in manual and automated 96 or 384-well formats.
Details
Specifications
Features
Specifications
Main Functions
Recover DNA fragments >100bp from agarose gel(<0.3g), purification of DNA from PCR, enzymatic reaction solution or crude gDNA
The Kit method contains magnetic particles in an optimized binding buffer to selectively bind DNA fragments (>100bp) and larger to paramagnetic beads. Excess primers, nucleotides, salts, and enzymes can be removed using a simple washing procedure.
Advantages
High recovery efficiency – up to 80% DNA recovery
General – recover DNA from gel or enzyme-driven reaction solutions such as PCR
Kit Contents
Contents
D500101
D500102
D500103
Purification Times
50 Preps
500 Preps
5000 Preps
Buffer GDP
30 ml
250 ml
3 x 900 ml
MagPure Particles
1.6 ml
15 ml
3 x 50 ml
Buffer DW1
20 ml
180 ml
2 x 800 ml
Elution Buffer(10mmTris, pH8.5)
10 ml
60 ml
500 ml
Storage and Stability
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
Document
A highly efficient, easily automated agarose gel or PCR purification system that delivers superior quality DNA with no salt carryover. Requiring no centrifugation or filtration. The Kit can be easily used in manual and automated 96 or 384-well formats.
Trichinellosis is caused by Trichinella spiralis, a parasitic nematode of pork, horse and wild animals. Humans can be infected by eating raw or undercooked meat from infected animals. Most infected people do not show any symptoms. However, in some cases, symptoms appear during intestinal stage (diarrhea and abdominal pain) and muscular stage (muscle pain, fever, edema). Diagnosis is based on signs and symptoms, but in many cases it is not conclusive for the diagnosis. Serological assays have an important place on the final diagnosis of the disease. The ELISA kit has shown appropriate performance for the serological screening of trichinellosis.
This product is manufactured by Bordier Affinity Products in Switzerland and distributed in Germany exclusively by Milenia Biotec.
Method/Platform
ELISA in microplate format
Range/Assay Sensivity
95% sensitivity, 98% specificity
Test Principle
The kit provides all the material needed to perform 96 enzyme-linked immunosorbent assays (ELISA) on breakable microtitration wells sensitized with Trichinella spiralisexcreted/secreted (E/S) larval antigens. Specific antibodies in the sample will bind to these antigens and washing will remove unspecific antibodies. The presence of parasite specific antibodies is detected with a Protein A – alkaline phosphatase conjugate. A second washing step will remove unbound conjugate. Revealing bound antibodies is made by the addition of pNPP substrate which turns yellow in the presence of alkaline phosphatase. Color intensity is proportional to the amount of Trichinella spiralis specific antibodies in the sample. Potassium phosphate is added to stop the reaction. Absorbance at 405 nm is read using an ELISA microplate reader. The test can be performed with automatic systems, but this must be validated by the user.
Trichinellosis is caused by Trichinella spiralis, a parasitic nematode of pork, horse and wild animals. Humans can be infected by eating raw or undercooked meat from infected animals. Most infected people do not show any symptoms. However, in some cases, symptoms appear during intestinal stage (diarrhea and abdominal pain) and muscular stage (muscle pain, fever, edema). Diagnosis is based on signs and symptoms, but in many cases it is not conclusive for the diagnosis. Serological assays have an important place on the final diagnosis of the disease. The ELISA kit has shown appropriate performance for the serological screening of trichinellosis.