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app/components/SampleGuideline/GeneralGuidelines.jsx

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+import React from 'react';
+
+const GeneralGuidelines = () => {
+  return (
+    <div className="space-y-6">
+      <div className="mb-6">
+        <h3 className="text-2xl font-semibold text-gray-600 mb-4">General Guidelines</h3>
+      </div>
+      
+      <div className="prose max-w-none">
+        <ul className="space-y-4 text-gray-700 leading-relaxed pl-5">
+          <li className="list-disc">
+            Please complete the Sample Initiation Form (SIF), ensuring that the
+            sample names on the form match the labels on the sample tubes. We also
+            request that you send an electronic copy of the form and any required QC
+            data via email.
+          </li>
+          <li className="list-disc">
+            Each tube should be labeled on the lid with a maximum of 4-6
+            alphanumeric characters (e.g., 4B0001). Use a black permanent marker to
+            write sample names on the top and side of each tube. Avoid writing
+            directly on the tube wall or cover with an oil pen.
+          </li>
+          <li className="list-disc">
+            DNA can be submitted in DNase-free water, Elution Buffer, or 10mM Tris
+            pH 8.0. DNA samples should have an OD260/280 ratio as close to 1.8~2.0
+            as possible. All DNA should be RNase-treated and free from degradation
+            or contamination. Ship with ice packs. The total amount of DNA required
+            depends on the specific application.
+          </li>
+          <li className="list-disc">
+            RNA can be submitted in RNase-free water, RNA Stabilization Reagent, or
+            10mM Tris pH 8.0. All total RNA samples should be DNA-free, with an OD
+            A260/A280 ratio ≥ 1.8, A260/230 ratio ≥ 1.8, and a RIN ≥ 6. Ship with
+            dry ice. The total amount of RNA required depends on the specific
+            application. For Long Read Sequencing, RNA samples should have a RIN ≥
+            8.
+          </li>
+          <li className="list-disc">
+            The listed concentrations should be determined by fluorometry (e.g.,
+            PicoGreen/Qubit/RiboGreen). If using spectrophotometry (e.g., Nanodrop),
+            increase concentrations by approximately twofold.
+          </li>
+          <li className="list-disc">
+            The quality inspection method for the sizes and concentrations of the
+            Ready To Run Library is Qubit and Agilent Bioanalyzer.
+          </li>
+        </ul>
+      </div>
+    </div>
+  );
+};
+
+export default GeneralGuidelines;