NYMU Taipei/phptest

From 2007.igem.org

(Difference between revisions)
Line 4: Line 4:
<script language="javascript">
<script language="javascript">
-
function CheckId(SI,SV){
+
function CheckId(SI,SV,CI,CV,VI,L){
var SI = SI;
var SI = SI;
var SV = SV;
var SV = SV;
 +
var CI = CI;
 +
var CV = CV;
 +
var VI = VI;
 +
var L  = L;
//document.write("insert is v1, and vector is v2");
//document.write("insert is v1, and vector is v2");
-
alert("insert size = " + SI + "(bp)\n");
+
alert("insert size = " + SI + "(bp)\n" + "vector size = " + SV + "bp\n" + "vector concentration = " + CV + "bp");
}
}

Revision as of 09:50, 16 September 2007

size (bp) of insert part (SI)
size (bp) of vector part (SV)
concentration (ug/uL) of insert (CI)
concentration (ug/uL) of vector (CV)
volume (uL) of insert for gel separation (VI)
volume (uL) of insert for ligation (L)

  • total digestion volume is 20 uL (typical)
    • enzyme 1 and enzyme 2 (1uL * 2)
    • 10X buffer (2uL)
    • BSA (2uL)
    • plasmid + ddH2O (14uL = VI + water, 1 <= VI <= 14)
    • for vector
      • we assume 300 ng for digestion and 90% loss
      • thus, amplify 10X from 300 ng to 3,000 ng = 3 mg
      • 3,000 ng = CV (ug/uL) * 1000 (ng/ug) * DVV, DVV (digested vector volume) = 3/CV
  • total gel separation volume is 50 uL
  • total ligation volume is 10uL
    • vector weight is 300 ng
    • 10X buffer (1uL)
    • ligase (1uL)
    • VV + L + water (8uL)
  • formula
    • 300 * SI * 3 * 10 (損失因子) / SV = CI * VI * L /50
    • vector weight is 300 ng
    • SI (bp) is size of insert
    • SV (bp) is size of vector
    • VI (uL) is volume of insert
    • VV (uL) is volume of vector
    • CI (ng/uL) is concentration of insert
    • CV (ng/uL) is concentration of vector
Retrieved from "http://2007.igem.org/wiki/index.php/NYMU_Taipei/phptest"