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Top : New Forum Archives (2009-): : General-Lab-Techniques
271. Prepared Slides Repair - (reply: 2)
272. 3D printing of (horizontal, agarose) gel trays, and other lab equipment - (reply: 6)
273. How to prepare BSA standards? - (reply: 1)
274. How do I calculate the enery absorved by cells form a UV light - (reply: 3)
275. seeking for FISH handbook etc - (reply: 6)
276. comet Assay - (reply: 2)
277. How do you process ascites sample from mice ? - (reply: 1)
278. A problem with basic concentrations and serial dilution calculations - (reply: 5)
279. Dissecting Pans - (reply: 3)
280. Obtain serum from clotted blood - (reply: 1)
281. Sodium Acetate Buffer pH 5.2 - (reply: 3)
282. sample analysis of "whole" vegetable - (reply: 4)
283. M2 antibody background in Xenopus cell extracts - (reply: 6)
284. Weirdest thing with DNA dye and agarose gel - (reply: 4)
285. How to calculate the concentration from Molar mass - (reply: 3)
286. Small volume of detergent - (reply: 2)
287. Rinsing and drying after using RNAse-zap - (reply: 1)
288. Separation of glycerol from protein - (reply: 6)
289. immunofluorescence - antibody choice for double staining - (reply: 2)
290. transformation and protein purification calculation help; very basic - (reply: 5)
291. Gloves turning yellow with use? - (reply: 5)
292. Low Qubit concentration - (reply: 2)
293. 16s rrna - (reply: 1)
294. software to draw biological diagram - (reply: 2)
295. Can somebody explain to me what "spiking" means in RT-PCR and why do you - (reply: 3)
296. DNA isolation from whole blood + clotting??!! - (reply: 2)
297. phospho-protein and total protein significance - (reply: 1)
298. Discard AW1, P2, P1. QC solution - (reply: 5)
299. DNA extraction problem - strange bands - (reply: 4)
300. Anyone else see GFP alone normally localize at the centrosome? - (reply: 10)