インフォメーション
X


Novabiochem Innovations

Merck:/topic/novabiochem/Merk_N1.jpg

Novabiochem Innovations provide highly detailed protocols, application examples, and tips and tricks on the use of a particular product or group of products.

No. 1/12: New high-load polar resins for SPPS
No. 4/11: New tools for native chemical ligation
No. 3/11: Use and applications of Dbz resins in native chemical ligations
No. 2/11: Step-wise Fmoc SPPS of ubiquitin probes
No. 1/11: Guide to the synthesis of phosphotyrosine related peptides by Fmoc SPPS
No. 3/10: Critical evaluation of in situ coupling reagents for SPPS
No. 2/10: Guide to the use of isoacyl dipeptides in Fmoc SPPS
No. 1/10: Total synthesis of the 101 residue d2 domain of VEGF receptor 1
No. 2/09: Non-explosive replacement for HOBt
No. 1/09: Synthesis of FBP28WW domains using pseudoproline and isoacyl dipeptides
No. 1/08: Overcoming aspartimide in Fmoc SPPS
No. 2/08: Synthesis of β-amyloid using an isoacyl dipeptide
No. 1/07: Synthesis of wild-type and phosphorylated phospholamban
No. 2/07: Synthesis of peptides containing methylated lysine residues
No. 3/07: Synthesis of the transmembrane region of bradykinin receptor
No. 4/07: Comparison of pseudoproline and isoacyl dipeptides in the synthesis of difficult peptides
No. 1/06: Synthesis of thymosin-α1 using pseudoproline dipeptides
No. 2/06: The role of HOBt in coupling reactions
No. 3/06: Synthesis of neurotoxic prion peptide (106 - 126)
No. 4/06: Smart peptide synthesis: Synthesis of PADRE-Muc chimeric peptide
No. 5/06: Synthesis of peptides containing arginine residues
No. 6/06: Smart peptide synthesis: Synthesis of the Rantes
No. 1/05: New tools for the SPPS of FRET peptides
No. 2/05: SPPS of biotinylated peptides
No. 3/05: Synthesis of highly amyloidogenic human IAPP using pseudoproline dipeptides
No. 4/05: New tools for SPPS of labeled peptides
No. 5/05: Expediting convergent synthesis with pseudoproline dipeptides
No. 6/05: Solid phase synthesis of AMC-based enzyme substrates
No. 1/04: Guidelines for the use of Pseudoproline Dipeptides
No. 2/04: Microwave accelerated Suzuki couplings employing a polymer-supported palladium phosphine
No. 3/04: Synthesis design using Pseudoproline Dipeptides
No. 4/04: Exploring strategies for peptide synthesis
No. 5/04: Strategies for the synthesis of peptide aldehydes
No. 6/04: Epimerization-free fragment condensation with pseudoproline (oxazolidine) dipeptide
No. 1/03: New derivatives for overcoming aspartimide formation
No. 2/03: Synthesis of long peptides using pseudoproline dipeptides
No. 3/03: IBX Polystyrene
No. 4/03: Stability of polymer-supports to microwave heating

© Merck KGaA, Darmstadt, Germany, 2012


x

Merck Milliporeへようこそ

 

ヨーロッパ、中東、アフリカ アジア / パシフィック 北アメリカ、中央アメリカ、カリブ 南アメリカ

国を選択してください：

北アメリカ、中央アメリカ、カリブ


南アメリカ


ヨーロッパ、中東、アフリカ


アジア / パシフィック


すべての国　AからZまで


国名が見つからない場合クリックしてください。 こちら.

 

x

Merck Chemicals Cart ()

You are entering the Millipore online shop. Both carts are maintained for you while you shop between sites. We recommend to complete your Merck order before visiting Millipore.com.

Go to Millipore Proceed to checkout


What kind of products are you looking for?

ミリポア

Bio manufacturing and Life science.

Merck Chemicals

High-quality industrial and laboratory chemicals.

重要なメッセージ

現在、バイオ製品と他のメルク製品を同時に注文することが出来ません。現在の注文を先にお済ませください。

現在の注文を済ませずに先へ進みますか？その場合ショッピングカートは空になります。