Flac 3D 6.0 for dynamic analysis?

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I have a time series data of some biochemical studies ( DNA and Chromosomal damage) which I intend to use to further predict into future ?

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No mRNA increase in PCR after successful transfection in ARPE-19 cells ?

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What is the easiest way to remove the water from organic solvents?

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Enhanced Yellow Fluorescent Protein (Aequorea victoria) DNA sequence?

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What kind of fluid could I use for a pitfall trap that also does not invalidate molecular testing?

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What's the best way to measure growth rates in House sparrow chicks from day 2 to day 10?

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Do we need to write protocol for a second study of a systematic review that has been registered and published?

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How to increase a model accuracy ?

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Do I need to do linear regression before running mediation analysis using PROCESS MACRO by Hayes ?

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Gel electrophoresis result for total RNA samples, 1.5 Agarose gel was used, How to improve the integrity of RNA?

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Sample dilution for quantitative analysis using ELISA?

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Is There Any Feasible Method To Test Fluorescent Compounds Other Than Fluorescence Spectrometers ??

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Alireza Rashiddel

Hello

Check the dynamic boundary conditions and damping and mesh size.

Give me more information on your project!

Best,

Rashiddel

Lecturer FLAC 2D - 3D software

Peter Antwi Buah

can i have your email address? please?

[email protected]

thanks

Nima Dolma Sherpa

hello can u help me in this issue...as well

Mohammad Azarafza

Dear Peter,

Regarding the dynamic analysis in FLAC3D you have to control the boundary condition and fixed regions, loading conditions, and material specification in model. Using dynamic loading required to applying a dynamic input boundary condition at either the model boundary or internal gridpoints. Please check the boundaries, loading and materials properly.

Bests,