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600-14-6

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关键词:'600-14-6'
显示 1-30 共 51 条结果 关于 "600-14-6" 范围 网站内容
凝血酶因子IIa
凝血酶因子IIa是一种内切丝氨酸蛋白酶,可选择性地裂解纤维蛋白原的Arg -Gly键,形成纤维蛋白并释放纤维蛋白肽A和B。
新型无异种和无血清成骨分化培养基中人间充质干细胞的加速骨细胞分化
新型无血清、无异种人间充质干细胞(MSC)骨细胞分化培养基的开发。
PCR/qPCR/dPCR实验设计
整个PCR工作流程易受引入变量的影响。许多变量无法避免,例如样本来源和逆转录步骤的要求。实验设计也波动较大,可能决定PCR的成败,影响实验的可重复性和灵敏度。
MSI检测和IHC
结直肠癌是大多数西方国家居民中普遍发生的疾病,仅次于肺癌。
Analytical Method: Lead (total) in effluents
Photometric determination with PAR subsequent to acid mineralisation; DIN decomposition
Analytical Method: Lead in waste water with high concentrations of calcium
Photometric determination with PAR subsequent to separation of lead with Sodium diethyldithiocarbaminate.
Plant/Fungi Total RNA Purification Kit
The Plant/Fungi Total RNA Purification Kit provides a rapid method for the isolation and purification of total RNA from a wide range of plant and filamentous fungal species.
MonoBeads: Purification of Milligram Quantities with Highest Resolution
This page covers using Monobeads for purification of proteins, peptides, or oligonucleotides.
Purification or Removal of Viruses including Adeno-associated Virus
This page shows how to purify or remove viruses with a Capto DeVirS, AVB Sepharose High Performance from Cytiva.
Peptide Labeling
Chromogenic and fluorogenic derivatives are invaluable tools for biochemistry, having numerous applications in enzymology, protein chemistry, immunology and histochemistry.
Purification of Histidine-Tagged Proteins Secreted into Eukaryotic Cell Culture Supernatants Using Ni Sepharose® Excel
This page shows how to purify histidine-tagged proteins secreted into eukaryotic cell culture supernatants using Ni Sepharose Excel from Cytiva.
Analytical Method: Sulfite in Shrimps
Method: Photometric determination with 2,2'-dinitro-5,5'-dithiodibenzoic acid (Ellman's reagent)
Performing an Isolation of Native Complexes
This page provides information about performing an isolation of natural multi-protein complexes for structural and functional studies using classical biochemical methods and products from Cytiva.
Purification or Removal of Proteins and Peptides
This page shows how to purify or remove proteins and peptides with exposed amino acids with Chelating Sepharose High Performance, Chelating Sepharose Fast Flow, Capto Chelating from Cytiva.
Faster Protein and Peptide Liquid Chromatography (FP2LC)
Larger porous shell particles with narrow particle size distribution, used in Supelco's BIOshell™ columns for the reversed-phase U/HPLC analysis of peptides and proteins, provide increased efficiency per unit pressure drop.
Early Detection of Cardiotoxicity Biomarkers | SMC® Technology
Cardiotoxicity biomarkers like cardiac troponin I (cTnI) in serum samples can be detected earlier with the ultrasensitive biomarker detection SMC® immunoassay platform. Discover the utility of Single Molecule Counting (SMC®) technology for the early assessment of heart muscle injury in
Thermoelectric Performance of Perovskite-type Oxide Materials
The prevailing strategies for heat and electric-power production that rely on fossil and fission fuels are having a negative impact on the environment and on our living conditions.
Sepharose Fast Flow: Purification with Good Resolution and Easy Scale-Up
This page covers the use of Sepharose Fast Flow for purification of proteins.
Multi-walled Carbon Nanotubes: Manufacturing, Characterization and Applications
Improved multi-walled carbon nanotubes (MWNTs) have been recently developed by CoMoCAT® technique and adopted in a significant number of applications, including batteries, water filter membranes, and electric or thermal conducting polymer composites.
Accelerated Osteocyte Differentiation of Human Mesenchymal Stem Cells in a Novel Xeno-free and Serum-free Osteogenesis Differentiation Media
Development of a novel serum-free and xeno-free human mesenchymal stem cell (MSC) osteocyte differentiation media.
Column Packing and Preparation for Size Exclusion Chromatography
Column Packing and Preparation for Size Exclusion Chromatography
A Review of Mesoporous TiO2 Thin Films
Titanium dioxide (TiO2) is an important n-type semiconducting material that shows interesting characteristics such as photoswitchable surface wettability, high photocatalytic activity, bistable electrical resistance states and high electron drift mobility.
Lysing Enzymes
Enzymes provide a non-mechanical method for cell lysis and protoplast preparation. It may seem like a simple process to throw in your enzyme, stick your tube in the water-bath and walk away, but what is actually going on in that
Smart Nanofiber Meshes as a Local Drug Delivery Platform
Professor Mitsuhiro Ebara provides insights on several types of smart nanofiber mesh systems that have been explored for different drug delivery purposes.
Purification of Membrane Proteins
This page shows how to perform a purification of His-tagged membrane proteins.
Electrospun Nanofibers for Drug Delivery Systems
Local delivery of bioactive molecules using an implantable device can decrease the amount of drug dose required as well as non-target site toxicities compared to oral or systemic drug administration.
Metal Borohydrides as Hydrogen Storage Materials
An article about metal borohydrides as hydrogen storage materials
Detection of Protein-protein Interactions by in situ PLA
Proteins are complex biological molecules essential for cellular structure and functions. The majority of proteins commonly interact with various molecules, including other proteins, in order to exert their functions.
MISSION® esiRNA Specifications
MISSION® esiRNA provides RNAi researchers with a proven, cost-effective, and simple way to perform RNAi screens
Synthesis of Melting Gels Using Mono-Substituted and Di-Substituted Alkoxysiloxanes
Synthesis of Melting Gels Using Mono-Substituted and Di-Substituted Alkoxysiloxanes
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