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Western Blot Analysis (Polyacrylamide-based)
Cat. #317



Show your students how the Western blot identifies proteins based on both antibody reactions and antigens. Proteins are separated on a denaturing SDS polyacrylamide gel and are transferred (blotted) to a nylon membrane. The membrane is then exposed sequentially to solutions containing primary antibody, followed by a secondary antibody coupled to an enzyme. The membrane is soaked in a substrate solution to develop the color reaction, which results in identifying the antigen as a band. The molecular weights of the visible bands are measured using prestained protein markers of known molecular weight. This experiment does not require an electrotransfer apparatus.



Kit includes: instructions, negative control, BSA - high and low concentration, anti-BSA protein antibody, secondary antibody conjugate, hydrogen peroxide, peroxide co-substrate, blocking buffer, powdered milk, PBS buffer, prestained protein standard marker, membrane and filter paper and electrophoresis buffer.

All you need: 3 polyacrylamide gels (12%), MV10 vertical gel electrophoresis apparatus, power supply, automatic micropipet with fine tips, trays for blot transfer, lab glassware, plastic wrap, metric rulers, methanol and glacial acetic acid.

  For 6 Blots

  Complete in 60 minutes, Blot Overnight, Detection 150 minutes


Want to learn more? Download a PDF of the instructions or email us with questions.

  Secure Ordering


Catalog #PriceQuantity

317$199
For 6 Blots

651$39
Pre-cast Polyacrylamide Gels (3)

652$74
Pre-cast Polyacrylamide Gels (6)



You may also place an order by phone, fax, email or regular mail:

E D V O T E K® -- The Biotechnology Education Company®
tel 800.338.6835 | fax 301.340.0582 |
info@edvotek.com
Post Office Box 341232; Bethesda, MD 20827-1232 USA








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