PDF Archive search engine
Last database update: 07 January at 20:58 - Around 220000 files indexed.
Results for «assay»:
Total: 50 results - 0.029 seconds
E3 Ligases 100%
For E3 ligase in vitro activity assays, we offer ELISA-based autoubiquitylation or substrate ubiquitylation assay and TR-FRET autoubiquitylation or substrate ubiquitylation assay.
It is therefore important to be able to accurately verify the activity of the CRISPR-Cas9 system in a given assay, in order to maximize the cleavage and gene knock-in/knock-out efficiency of CRISPR-Cas9.
The QuickPlex has a wide menu of commercially available assay kits and a full line of components and reagents for developing your own assays.
Generally compatible with your existing ELISA without assay re-design The increase in sensitivity and precision enable other potential benefits:
Development and Clinical Implications of a Novel Assay, Pilot Validation with a Five-Point Grading Scale, and Evaluation of Six U.S.
ELISA or Enzyme- link immunosorbe nt assay is the technique used to detect the presence of antibodies in the blood.
Contact us Synbio Technologies 1 Deer Park Drive, Suite L-1 Monmouth Junction NJ, 08852 Tel:+1 732-230-3003 Fax:+1 609 228 5911 Web:www.synbio-tech.com E-mail:firstname.lastname@example.org Comprehensive Functional Assay:
Fluorescent In Situ Hybridization (FISH) Assay Fluorescent In Situ Hybridization (FISH) Assay 1 2 3 4 What is FISH？ Definition, Principle and Sample Types Probes The core of FISH technology FISH Procedure A quick and simple FISH protocol Application Wide range of uses and bright prospects Content 输入标题文本 What is Fluorescent in situ hybridization (FISH) ?
The LAL test became the assay of choice for bacterial endotoxins worldwide because of its specificity, simplicity and remarkable sensitivity.
www.elsevier.com/locate/meegid Short communication Diﬀerences in rpoB, katG and inhA mutations between new and previously treated tuberculosis cases using the GenoType MTBDRplus assay T ⁎ Gerardo Alvarez-Uria , Raghuprakash Reddy a b Department of Infectious Diseases, Rural Development Trust Hospital, Bathalapalli, AP, India Department of Microbiology, Rural Development Trust Hospital, Bathalapalli, AP, India.
Interleukin-8 (IL-8) production was measured by Enzyme Linked ImmunoSorbent Assay, mRNA transcription of pro-inflammatory cytokines by microarrays or RNase Protection Assay.
We monitored the humoral response, of the four responders, to CTAs by High Throughput Immunoblot assay (HTI), 29 CTAs were bound in a concise pattern to nitrocellulose filters and developed in the following methodology.
We conclude that a 51 panel multigene blood transcript analysis is significantly more sensitive and efficient (>93%) than any single analyte assay (CgA, PST or NKA) for NET detection.
Enzyme-linked Immunoabsorbent Assay;
J Chromatogr A 1167, 2007, 195 201 Journal of Chromatography A, 1167 (2007) 195–201 Quantitative determination of 4-ethylphenol and 4-ethyl-2-methoxyphenol in wines by a stable isotope dilution assay Sierra Rayne, Nigel J.
4-Ethylphenol and 4-ethylguaiacol concentrations were determined in 188 barreled red wine samples from commercial wineries in the Okanagan Valley appellation of British Columbia, Canada using a stable isotope dilution assay (SIDA).
Acetyl-L-Carnitine HCL 10110420130804 1000kg China August.03,2013 August.02,2015 Item Appearance Identification Appearance of Solution Specific Rotation pH Loss on Drying Assay Residue on ignition Standard White crystalline powder IR Clear and Colourless -26.0° ~-29.0° 2.3~2.6 <0.5% 98.5%~102.0% <0.5% Results White crystalline powder Positive Clear and Colourless -27.62°