TGM12 Table top capillary vessel Haematocrit centrifuge
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TGM12 Table top capillary vessel Haematocrit centrifuge
Application:
Measure the ratio of blood corpuscle and separate microblood and micro solution.
Model: TGM12 Table top high speed capillary vessel centrifuge
Features:
Brushless DC motor, free maintenance, no powder pollution, micro computer control, digital display indicates the time、speed and RCF. Electric lid lock、 over speed and imbalance protection. The centrifuge body is made of high quality steel, Safe and reliable.
Technical parameters:
Max speed
12000r/min
Max RCF
15800×g
Time range
1~99min
Speed accuracy
±20r/min
capacity
24pieces capillary vessel
Noise
≦55dBA
Weight
13KG
Dimension
355×270×205mm
Packaged weight
15KG
Packaged dimension
455×335×270mm
Power
AC 220V 50HZ 5A
Motor
Brushless
Package
Carton box
Other Products
XTL-65 Series Zoom Stereo Microscope
Product Info
Document
Product Info
Specification
6.5-65 x continuous zoom stereo microscope
XTL-6565A
XTL-6565B
XTL-6565D
XTL-6565C
Zoom Body
Binocular head,45°decline,360°rotate
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Zoom Body
Trinocular head,45°decline,360°rotate
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Eyepiece
WF10X22mm
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Objective
zoom objective 0.65X—6.5X
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Zoom Rate
1:10
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Total Amplific- ation Rate
the standard configuration is 6.5X-65X
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Auxiliary Lens
0.3X,0.5X,0.7X,1X,1.5X,2X For Option
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O
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O
WorkingDistance
110mm
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Djopte
55mm-75mm
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Focus arm
76mm Diameter,32mm pole size
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plate
Black/White plate,Glass plate for option
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Dptiona
Stand
O
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Stand
BL3 base,column support upper and lower light source 3 WLED
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Stand
811 base column support large flat base has no light source
Short term stability: 2-8oC, Long term stability: See individual component labels
Stability:
> 2 years under recommended storage conditions
Analyte:
endo-Cellulase
Assay Format:
Spectrophotometer, Auto-analyser
Detection Method:
Absorbance
Wavelength (nm):
400
Signal Response:
Increase
Limit of Detection:
1.2 x 10-3 U/mL
Reproducibility (%):
~ 3%
Total Assay Time:
10 min
Application examples:
Fermentation broths, industrial enzyme preparations and biofuels research.
Method recognition:
Novel method
The K-CellG5-2V pack size has been discontinued (read more).
Cellulase Activity Assay Kit.
The CellG5 assay reagent for the measurement of endo-cellulase (endo-1,4-β-glucanase) contains two components; 1) 4,6-O-(3-Ketobutylidene)-4-nitrophenyl-β-D-cellopentaoside (BPNPG5) and 2) thermostable β-glucosidase. The ketone blocking group prevents any hydrolytic action by the β-glucosidase on BPNPG5. Incubation with an endo-cellulase generates a non-blocked colourimetric oligosaccharide that is rapidly hydrolysed by the ancillary β-glucosidase. The rate of formation of 4-nitrophenol is therefore directly related to the hydrolysis of BPNPG5 by the endo-cellulase. The reaction is terminated and the phenolate colour is developed on addition of Tris buffer solution (pH 9.0).
The CellG5 assay represents a huge step forward in the methodology for the measurement of cellulase that traditionally relied on substrates such as CM-cellulose, Avicel, cellooligosaccharides, filter paper or dyed polysaccharides including CMC Congo red or cellulose azure.
The CellG5 assay reagent for the measurement of endo-cellulase (endo-1,4-β-glucanase) contains two components; 1) 4,6-O-(3-Ketobutylidene)-4-nitrophenyl-β-D-cellopentaoside (BPNPG5) and 2) thermostable β-glucosidase. The ketone blocking group prevents any hydrolytic action by the β-glucosidase on BPNPG5. Incubation with an endo-cellulase generates a non-blocked colourimetric oligosaccharide that is rapidly hydrolysed by the ancillary β-glucosidase. The rate of formation of 4-nitrophenol is therefore directly related to the hydrolysis of BPNPG5 by the endo-cellulase. The reaction is terminated and the phenolate colour is developed on addition of Tris buffer solution (pH 9.0).
Tumor-Associated Glycoprotein 72 (TAG-72) is a glycoprotein found on the surface of many cancer pathologies. Anti-TAG-72 can be useful for detecting some adenocarcinomas and non-neoplastic tissues. This diagnostic grade TAG-72 IVD antibody is useful for identifying adenocarcinomas in positive staining, but in mesotheliomas no staining is observed.
