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           Search results for: 4-Bromo-2-methoxybenzoic acid CAS: [72135-36-5]    

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First Comprehensive Study of a Giant Among the Insects, : Basic Facts from Its Biochemistry, Physiology, and Anatomy.

is one of the largest insects in the world, but unfortunately, there is a lack of basic information about its biology. Previous papers have mostly described morphology or taxonomy, but studies concerning its anatomy and physiology are largely absent. Thus, we employed microscopic, physiological, and analytical methods to partially fill this gap. Our study focused on a detailed analysis of the antennal sensilla, where coeloconic sensilla, grouped into irregularly oval fields, and sensilla trichoidea were found. Further, the inspection of the internal organs showed apparent degeneration of the gut and almost total absence of fat body. The gut was already empty; however, certain activity of digestive enzymes was recorded. The brain was relatively small, and the ventral nerve cord consisted of three ganglia in the thorax and four ganglia in the abdomen. Each testis was composed of approximately 30 testicular follicles filled with a clearly visible sperm. Chromatographic analysis of lipids in the flight muscles showed the prevalence of storage lipids that contained 13 fatty acids, and oleic acid represented 60% of them. Some of our findings indicate that adult rely on previously accumulated reserves rather than feeding from the time of eclosion.

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Bone giant cell tumor tis Mouse anti human FGF basi Rabbit anti PKC theta (Ab Androgen Receptor (Phosph Andrographolide CAS Numbe Anti Androgen Receptor pr Androst-4-ene-3,6,17-trio FDA Standard Frozen Tissu 3-O-Acetyl-17-O-tert-buty Normal rat multiple organ CAR,Car,Constitutive andr ∆1-Androstene-3α,17β-

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Production of bioethanol from unwashed-pretreated rapeseed straw at high solid loading.

Reduction in water consumption and increase in ethanol concentration are two main challenges for bioethanol production from lignocellulosic materials. To address the two challenges, the aim of this work was to study the production of bioethanol from unwashed-pretreated rapeseed straw (RS) at high solid loading. RS pretreated with 1% (w w) HSO at 160 °C for 10 min resulted in excellent digestibility and fermentability of pretreated RS. The unwashed-pretreated RS was subjected to presaccharification and fed-batch simultaneous saccharification and fermentation (P-FB-SSF) at a final solid loading of 22% (w w). Ethanol concentration and ethanol yield of 53.1 g L (equivalent to 4.1% (w w) based on fermentation slurry) and 72.4% were obtained, respectively. In total, 92.1 g water g ethanol was consumed, a much smaller amount than that observed with washing after pretreatment or fermentation performed at lower solid loading.

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Z-ATAD-FMK; Appearance Ly Atherosclerosis (Human) A Red Load Taq Master high Z-ATAD-FMK; Appearance Ly Red Load Taq Master high Atherosclerosis (Mouse) A Ro 31-8220 methanesulfona Cytokine (Mouse) Antibody Anti-Human ATPase (195-20 Itraconazole; Appearance Anti ATXN10(Ataxin 10) (C AccuPower HotStart PCR Pr

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Siderophores from the Entomopathogenic Fungus .

We report NMR- and MS-based structural characterizations of siderophores and related compounds from (Balsamo-Crivelli) Vuillemin, including ten new chemical entities (-, -, -, and ) and five known compounds, (, , , , and ). The siderophore mixture from ARSEF strain #2680 included two compounds in which -mevalonyl--hydroxyornithine replaces both () or one () of the -anhydromevalonyl--hydroxyornithine units of dimerumic acid (). Mevalonolactone () was present as a degradation product of and . ARSEF #2860 also produced compounds that have mannopyranose () or 4--methyl-mannopyranose units (, ), two compounds (, ) that can be rationalized as 4--methyl-mannopyranosyl analogues of the esterifying acid moieties of metachelins A and B, respectively, and two probable decomposition products of , a nitro compound () and a formate (). Beauverichelin A (), a coprogen-type siderophore that represents the di-4--methyl-mannopyranosyl analogue of metachelin A, was detected in crude extracts of ARSEF #2860, but only in trace amounts. ARSEF strains #252 and #1955 yielded beauverichelin A in quantities that were sufficient for NMR analysis. Only the di- (-) and trihydroxamate () siderophores showed iron-binding activity in the CAS assay and, when ferrated, showed strong ESIMS signals consistent with 1:1 ligand/iron complexes.

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Rabbit anti PKC theta (Ab Periodic Acid Schiff (PA Theophylline CAS Number [ Normal mouse multiple org MyGenie 96 Gradient Therm Tube Strips 8 thermo Stri Thermostable TDG Kit Recombinant Human PKC the BACTERIOLOGY BACTEROIDES Theobromine CAS Number [8 FDA Standard Frozen Tissu Multiple organ tumor tiss

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High-throughput and all-solution phase African Swine Fever Virus (ASFV) detection using CRISPR-Cas12a and fluorescence based point-of-care system.

Here we report the development of a high throughput, all-solution phase, and isothermal detection system for African Swine Fever Virus (ASFV). CRISPR-Cas12a programmed with a CRISPR RNA (crRNA) is used to detect ASFV target DNA. Upon ASFV DNA binding, the Cas12a/crRNA/ASFV DNA complex becomes activated and degrades a fluorescent single stranded DNA (ssDNA) reporter present in the assay. We combine this powerful CRISPR-Cas assay with a fluorescence-based point-of-care (POC) system for rapid and accurate virus detection. Without nucleic acid amplification, a detection limit of 1 pM is achieved within 2 h. In addition, the ternary Cas12a/crRNA/ASFV DNA complex is highly stable at physiological temperature and continues to cleave the ssDNA reporter even after 24 h of incubation, resulting in an improved detection limit of 100 fM. We show that this system is very specific and can differentiate nucleic acid targets with closely matched sequences. The high sensitivity and selectivity of our system enables the detection of ASFV in femtomolar range. Importantly, this system features a disposable cartridge and a sensitive custom designed fluorometer, enabling compact and simple ASFV detection, intended for low resource settings.

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The acidic nature of "NMR-invisible" tri-coordinated framework aluminum species in zeolites.

The unambiguous characterization of different acid sites in zeolites is of great importance for understanding their catalytic performance and the rational design of highly efficient zeolite catalysts. In addition to various well-characterized extra-framework Al species, a tri-coordinated framework aluminum species can also serve as a Lewis acid site in zeolites, which is "NMR-invisible" owing to its extremely distorted local environment. Here we provide a feasible and reliable approach to elucidate the acidic nature of the tri-coordinated framework Al in dehydrated H-ZSM-5 zeolites sensitivity-enhanced two-dimensional (2D) multiple nuclear correlation NMR experiments coupled with trimethylphosphine oxide (TMPO) probe molecules. Two types of tri-coordinated framework Al sites have been unambiguously identified, which amount to 11.6% of the total Brønsted and Lewis acid sites. Furthermore, it was found that synergistic effects arising from the close spatial proximity between the tri-coordinated framework Al site and the Brønsted acid site lead to the generation of superacidity (with an acid strength stronger than 100% HSO) in the zeolite.

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INPP5F antibody Source Ra ELISA Microplate Reader ( Influenza A H5N1 (Avian F FDA Standard Frozen Tissu Interferon alpha-6 antibo Thermal Shaker with cooli Monkey Interleukin-4(IL4) Integrin alphaX antibody Integrin β1 (CD29) Antib Integrin alpha6 antibody Integrin â3 (Phospho Tyr FDA Standard Frozen Tissu

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Determination of sulphonated quinophthalones in Quinoline Yellow and its lakes using high-performance liquid chromatography.

Quinoline Yellow (QY, Colour Index No. 47005) is internationally used as a colour additive in foods, drugs, and cosmetics. The manufacture of QY requires sulphonating quinophthalone, and depending on the degree of sulphonation, various forms of QY result, containing different proportions of quinophthalone mono-, di-, and trisulfonic acid sodium salts (monoSA, diSA, and triSA, respectively). Regulations on the specific composition and uses of QY differ across countries with associated differences in names for QY. The QY form certified for use in the U.S. in drugs and cosmetics is known as D&C Yellow No. 10 (Y10). The Code of Federal Regulations (CFR) specifies that Y10 and its lakes consist of predominantly monoSA's, the sum of whose levels is ≥ 75%, and that the sum level of diSA's is ≤ 15%, with one of them (6'8'diSA) at ≤ 3%. The present work reports the development of an HPLC method for determining those CFR-specified values and the level of a non-CFR-specified component, 6'8'5triSA. The selected analytes, 6'SA, 6'5diSA, 6'8'diSA, and 6'8'5triSA, were quantified by using five-point-calibration curves (R > 0.999) with data-point ranges of 9.96-96.53%, 0.54-21.69%, 0.10-5.00%, and 0.11-5.53% by weight, respectively. The method was found to be precise (relative standard deviation values, 0.55-0.80%) and accurate (recovery values, 91.07-99.45%). LOD and LOQ values, respectively, were as follows: 1.23 and 3.70%, 6'SA; 0.42 and 1.26%, 6'5diSA; 0.11 and 0.34%, 6'8'diSA; and 0.01 and 0.04%, 6'8'5triSA. The HPLC method was applied successfully to the analysis of 20 Y10 and eight Y10 lake samples. It can be extended to other QY forms such as E104 and Yellow 203 because it enables analysis of 6'8'5triSA. This paper also addresses the implications of the varying structure depictions and CAS numbers of the QY components that are due to the existence of three tautomeric forms of quinophthalone.

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EnzyChrom™ Kinase Assay Colon cancer high density Caspase-9 Inhibitor Z-LEH Caspase-12 Inhibitor Z-AT High density (188 cases 2 Caspase-13 Inhibitor LEED ELISA Human , Interleukin Caspase-Family Inhibitor Caspase-1 Inhibitor Z-YVA Cathepsin B&L Inhibitor Z Caspase-8 Inhibitor Z-IET Human high sensitivity in

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