PROTIGA

   INC

 
 

 

More than 10 Years of MicrowaveBlue
 
Catalog # Product Description Quantity

    Price         
P1001 MicrowaveBlue trial kit Info       each   24.50
P1002-MWB MicrowaveBlue stain solution Info    500 ml   67.50
P1002-S2L MicrowaveBlue stain solution Info      2 liter 225.00
P1003 MWB-FinalTouch solution Info    500 ml   27.00
P2001 5x SDS loading buffer, non-reducing      50 ml   49.00

Ordering by phone: 301-606-5121,
or email,

or online
through Capital Biosciences: 2 Liter bottle, 500 ml bottle, all our Products
or through Fisher Scientific: 2 Liter bottle, 500 ml bottle

We accept: 

Refund Policy: Refunds will be given within 30 days after return of the product.

 

Process Development Consulting

and

Research and Development Consulting

 

While many proteins can be purified using standard protocols, we at PROTIGA, INC. have specialized in purifying those proteins that are more challenging. We take pride in tackling problems you may encounter during your purification and/or scale-up.

Why us? Unlike other companies, your project will be handled completely by a Ph.D at PROTIGA, INC who has had extensive experience with enzyme and protein purifications since 1980. We are fully committed to your project, and being an INTJ (Myers-Briggs type) you can expect Competence, Excellence and Intellectual Insight along with Creative Approaches to solve your problem.

What can we do for you? We will develop a GMP compatible and scalable protein purification process using state-of-the-art procedures and materials. We will work at a scale that is suitable for R&D, which will enable you to get enough material for proof of concept, feasibility and eventually Phase I studies.

You may consider having your procedure verified by us and, if necessary, optimized before filing for FDA approval. We work under strict confidentiality and will have a Material Transfer Agreement and a Confidentiality Agreement signed with you before starting to work on your project.

To get a drug on the market, the goal is to develop a process that satisfies FDA regulations, is fast and easy to perform, and scalable from very small to very large quantities. Skimping at the front end has cost many companies millions of dollars. Why? Their process had to be changed after it was filed; their process was more lengthy and cumbersome than necessary and inflicted more costs in the GMP environment than would have been necessary. This can be minimized or avoided by figuring all the factors in from the beginning and honing the procedure to perfection albeit keeping a wide tolerance margin. When successful, all the money spent on the R&D will pay off several-fold when the process goes into GMP. That is the philosophy of Lean Management: money spent upfront to set up an efficient system more than pays in the long run.