Tetra(3-methoxy-N-(PEG5-prop-2-ynyl)propanamide) Methane is a branched crosslinker with four terminal propargyl groups. The propargyl groups can react with azide compounds or biomolecules via copper catalyzed Click Chemistry to form a stable triazole linkage.
Detail
Tetra(3-methoxy-N-(PEG5-prop-2-ynyl)propanamide) Methane is a branched crosslinker with four terminal propargyl groups. The propargyl groups can react with azide compounds or biomolecules via copper catalyzed Click Chemistry to form a stable triazole linkage.
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TDL5E Bench top low speed refrigerated centrifuge machine
Product Info
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Product Info
TDL5E Bench top low speed refrigerated centrifuge machine
Application:
Widely used in the field of biochemistry, biological products, pharmaceutical factory and laboratory.
TDL5E Technical Parameters:
Max. Speed
5000rpm
Max.RCF
4420xg
Max. Volume
4x180ml
Speed Accuracy
±20rpm
Timer
1~99h59min
Noise
≤60dBA
Dimension(LxWxHmm)
570x600x340mm
Net Weight
76Kg
Power Supply
AC220V/110V 50HZ/60HZ
Temperature Range
-20℃~40℃
Temperature Accuracy
±1℃
Certifications
CE, ISO & Calibration report is available.
Matched Rotors for TDL5E:
Order No.
Rotor Type
Max. Speed(rpm)
Volume(ml)
Max.RCF(xg)
5E-1
Swing rotor
4000
4x180ml
2580
5E-2
Microplate rotor
4000
2x3x96well
2020
5E-3
Swing rotor
5000
4x1x50ml
4420
5E-4
Swing rotor
5000
4x1x100ml
4420
5E-5
Swing rotor
4000
4x2x50ml
2820
5E-6
Swing rotor
4000
4x4x15ml
2820
5E-7
Swing rotor
4000
4x6x10/7ml
2580
5E-8
Swing rotor
4000
4x6x5ml
2170
5E-9
Swing rotor
4000
4x4x10/7ml
2580
5E-10
Swing rotor
4000
4x4x5ml
2170
5E-11
Fixed rotor
5000
6x15ml
2540
5E-12
Fixed rotor
5000
12x15ml
3080
5E-13
Fixed rotor
5000
24x15ml
3500
5E-14
Fixed rotor
5000
4x50ml
2520
5E-15
Fixed rotor
5000
6x50ml
2850
5E-16
Fixed rotor
5000
4x100ml
2630
5E-17
Fixed rotor
5000
6x100ml
3130
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TDL5E is a table top low speed refrigerated centrifuge widely used in the field of biochemistry, biological products, pharmaceutical factory and laboratory.
D3182D HiPure Circulating DNA Midi Spin Kit D (Spin Protocol)
Product Info
Document
Product Info
Introduction
Free-circulating nucleic acids, such as tumor-specific extracellular DNA fragments and mRNAs in the blood or fetal nucleic acids in maternal blood, are present in serum or plasmausually as short fragments, <1000bp(DNA). HiPure Circulating DNA Midi Kit enables efficient purification of these circulating nucleic acids from human plasma, serum, or urine. The extracted products can be used for clinical in vitro detection.
Details
Specifications
Features
Specifications
Main Functions
Isolation circulating DNA from 1-5ml plasma, serum, bodyfluids by spin
Applications
qPCR, liquid or solid chip analysis, hybridization and SNP detection, etc.
Purification method
Mini spin column
Purification technology
Silica technology
Process method
Manual (centrifugation)
Sample type
Serum, plasma and other cell-free fluid samples
Sample amount
1-5ml
Elution volume
≥50μl
Time per run
≤70 minutes
Liquid carrying volume per column
4ml
Binding yield of column
1mg
Principle
This product is based on silica gel purification. The sample is lysed and digested with lysate and protease, DNA is released into the lysate. Transfer to an adsorption plate and filter column. Nucleic acid is adsorbed on the membrane, while protein is not adsorbed and is removed with filtration. After washing proteins and other impurities, nucleic acid was finally eluted with low-salt buffer (10 Mm Tris,pH 8.0).
Advantages
High yield – most optimal process, free DNA (>50bp) can be obtained to the maximum extent
High concentration – low elution volume, ensuring high nucleic acid concentration
High purity – low alcohol binding method, completely removing inhibitor and protein pollution
High recovery – DNA can be recovered at thelevel of PG by silica gel column purification
Kit Contents
Contents
D318203D
Purification Times
50 Preps
Buffer ACL
250 ml
Buffer ACB*
300 ml
Buffer DCW1*
22 ml
Buffer DCW2*
10 ml
Proteinase K
540 mg
Protease Dissolve Buffer
30 ml
Carrier RNA
110 μg
Nuclease Free Water
20 ml
HiPure CFDNA Mini Columns
50
2 ml Collection Tubes
100
Extender Tubes
50
Sealing O-Ringes
50
50ml Collection Tube
50
Support Tube
50
Storage and Stability
Proteinase K, Carrier RNA should be stored at 2-8°C upon arrival. However, short-term storage (up to 12weeks) at room temperature (15-25°C) does not affect their performance. The remaining kit components can be stored dry at room temperature (15-25°C) and are stable for at least 18 months under these conditions. The entire kit can bestored at 2-8°C, but in this case buffers should be redissolved before use. Make sure that all buffers are at room temperature when used.
Document
Free-circulating nucleic acids, such as tumor-specific extracellular DNA fragments and mRNAs in the blood or fetal nucleic acids in maternal blood, are present in serum or plasmausually as short fragments,
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.