OT-2 HEPA Module

Specification

7-50x    continuous    zoom    stereo    microscope		XTL-205A	XTL-205B	XTL-204A	XTL-2048	XTL-203A	XTL-203B
Zoom      Body	Binocular head,45°decline,360°rotate	●		●		●
	Trinocular head,45°decline,360*rotate		●		●		●
Eyepiece	WF10X22mm	●	●	●	●	●	●
Objective	zoom objective 0.7X—5X	●	●	●	●	●	●
Zoom     Rate	0.1:07.1	●	●	●	●	●	●
Total Amplific- ation   Rate	the standard configuration is 7X-50X	●	●	●	●	●	●
Auxiliary Lens	0.5X,0.7X,1X,1.5X,2X For Option	O	O	O	O	O	O
WorkingDistance	100mm	●	●	●	●	●	●
Diopter	55mm-75mm	●	●	●	●	●	●
Focus    arm	76mm Diameter,32mm pole size	●	●	●	●	●	●
Plate	Black/White plate,Glass plate for option	●	●	●	●	●	●
Optional	Stand	Q	Q
Stand	BI3 base.column sunnort unner and ower light source 3 WLED			●	●
	BL3-A base vertical arm bracket upper and lower light source 3 WLED	●	●
	B3 base column support has no light source					●	●
External light source	LED illumination	Q	Q	Q		O
Optiona	Photography,camera accessories CCD Coupler	o	o	o	o	o	o
Optional	Display attachment Monitor

K-AMYLSD

SKU: 700004263

160 assays (manual) / 640 assays (auto-analyser)

Description 

The ExcelDye™ 6× DNA Loading Dye (Tri-Color) is pre-mixed buffer for tracking the DNA sample during the electrophoresis on agarose or polyacrylamide gels. It contains three dyes (Xylene cyanol FF, Bromophenol blue, Orange G) for tracking the DNA migration. The Xylene cyanol FF, Bromophenol blue and Orange G migrate at approximately 800 bp, 150 bp and 30 bp on a standard 2% TAE agarose gel respectively (4,000 bp, 500 bp and 50 bp on 1% TAE agarose gel respectively). The included glycerol keeps the DNA at the bottom of the well and the presence of EDTA chelates divalent metal ions to prevent the process of metal-dependent nuclease. 

Composition 

• 0.03% Xylene cyanol FF 
• 0.03% Bromophenol blue
• 0.15% Orange G 
• 10 mM Tris-HCl (pH 8.0) 
• 60% glycerol 
• 60 mM EDTA

Storage 

4°C for 12 months
-20°C for 36 months

The ExcelDye™ 6× DNA Loading Dye (Tri-Color) is pre-mixed buffer for tracking the DNA sample during the electrophoresis on agarose or polyacrylamide gels. It contains three dyes (Xylene cyanol FF, Bromophenol blue, Orange G) for tracking the DNA migration. The Xylene cyanol FF, Bromophenol blue and Orange G migrate at approximately 800 bp, 150 bp and 30 bp on a standard 2% TAE agarose gel respectively (4,000 bp, 500 bp and 50 bp on 1% TAE agarose gel respectively). The included glycerol keeps the DNA at the bottom of the well and the presence of EDTA chelates divalent metal ions to prevent the process of metal-dependent nuclease.