66 lines
3.1 KiB
JavaScript
66 lines
3.1 KiB
JavaScript
import React from 'react';
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const GeneralGuidelines = () => {
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return (
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<div className="space-y-6">
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<div className="mb-6">
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<h3 className="text-3xl font-bold text-teal-700 mb-4">General Guidelines</h3>
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</div>
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<div className="prose max-w-none">
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<ul className="space-y-4 text-gray-700 leading-relaxed pl-5" style={{listStyleType: 'disc'}}>
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<li className="list-disc" style={{color: '#faae31'}}>
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<span style={{color: '#374151'}}>
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Please complete the Sample Initiation Form (SIF), ensuring that the
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sample names on the form match the labels on the sample tubes. We also
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request that you send an electronic copy of the form and any required QC
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data via email.
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</span>
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</li>
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<li className="list-disc" style={{color: '#faae31'}}>
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<span style={{color: '#374151'}}>
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Each tube should be labeled on the lid with a maximum of 4-6
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alphanumeric characters (e.g., 4B0001). Use a black permanent marker to
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write sample names on the top and side of each tube. Avoid writing
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directly on the tube wall or cover with an oil pen.
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</span>
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</li>
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<li className="list-disc" style={{color: '#faae31'}}>
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<span style={{color: '#374151'}}>
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DNA can be submitted in DNase-free water, Elution Buffer, or 10mM Tris
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pH 8.0. DNA samples should have an OD260/280 ratio as close to 1.8~2.0
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as possible. All DNA should be RNase-treated and free from degradation
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or contamination. Ship with ice packs. The total amount of DNA required
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depends on the specific application.
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</span>
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</li>
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<li className="list-disc" style={{color: '#faae31'}}>
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<span style={{color: '#374151'}}>
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RNA can be submitted in RNase-free water, RNA Stabilization Reagent, or
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10mM Tris pH 8.0. All total RNA samples should be DNA-free, with an OD
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A260/A280 ratio ≥ 1.8, A260/230 ratio ≥ 1.8, and a RIN ≥ 6. Ship with
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dry ice. The total amount of RNA required depends on the specific
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application. For Long Read Sequencing, RNA samples should have a RIN ≥
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8.
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</span>
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</li>
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<li className="list-disc" style={{color: '#faae31'}}>
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<span style={{color: '#374151'}}>
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The listed concentrations should be determined by fluorometry (e.g.,
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PicoGreen/Qubit/RiboGreen). If using spectrophotometry (e.g., Nanodrop),
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increase concentrations by approximately twofold.
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</span>
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</li>
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<li className="list-disc" style={{color: '#faae31'}}>
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<span style={{color: '#374151'}}>
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The quality inspection method for the sizes and concentrations of the
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Ready To Run Library is Qubit and Agilent Bioanalyzer.
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</span>
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</li>
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</ul>
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</div>
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</div>
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);
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};
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export default GeneralGuidelines; |