Academic literature on the topic 'Acid Red-14'
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Journal articles on the topic "Acid Red-14"
Anjali, Goel, Lasyal Rajni, and Abhilasha. "Mechanistic insight into oxidative degradation of some azo dyes with kinetic and thermodynamic analysis." Journal of Indian Chemical Society 93, Jun 2016 (2016): 621–25. https://doi.org/10.5281/zenodo.5638580.
Full textFalahul Alam, Riesma Azhar, Hilda Aprilia Wisnuwardhani, and Rusnadi Rusnadi. "Optimasi Pereaksi Warna Carik Uji untuk Analisis Kualitatif Kalium Bromat pada Makanan." Jurnal Ilmiah Farmasi Farmasyifa 1, no. 1 (2017): 62–68. http://dx.doi.org/10.29313/jiff.v1i1.3077.
Full textVinitnantharat, S., W. Chartthe, and A. Pinisakul. "Toxicity of reactive red 141 and basic red 14 to algae and waterfleas." Water Science and Technology 58, no. 6 (2008): 1193–98. http://dx.doi.org/10.2166/wst.2008.476.
Full textVenkatesh, Smita, and K. Venkatesh. "Ozonation for Degradation of Acid Red 14: Effect of Buffer Solution." Proceedings of the National Academy of Sciences, India Section A: Physical Sciences 90, no. 2 (2019): 209–12. http://dx.doi.org/10.1007/s40010-018-0583-6.
Full textBanin, M. M., S. Nurdiana, A. Emmawati, M. Rohmah, and A. Rahmadi. "Vitamin C, total titrated acid and antioxidant activity of Oximata® jelly mix." Food Research 6, no. 4 (2022): 295–303. http://dx.doi.org/10.26656/fr.2017.6(4).431.
Full textShen, Bing, Hong-Cui Liu, Wen-Bin Ou, et al. "Toxicity induced by Basic Violet 14, Direct Red 28 and Acid Red 26 in zebrafish larvae." Journal of Applied Toxicology 35, no. 12 (2015): 1473–80. http://dx.doi.org/10.1002/jat.3134.
Full textA., Y. ABO EL-AAL, I. MOSTAFA O., M. EL-SAYED GALILA, and S. MOURSY N. "Effect of Electrolytes and Organic Solvents on the Aggregation of some Acid Dyes." Journal of Indian Chemical Society Vol. 73, Apr-May 1996 (1996): 169–72. https://doi.org/10.5281/zenodo.5891765.
Full textMATEJA, KERT, and PODLIPNIK ČRTOMIR. "Influence of dye structure and temperature on the adsorption of acid dyes onto polyamide 6 knitwear." Industria Textila 70, no. 01 (2019): 3–8. http://dx.doi.org/10.35530/it.070.01.1400.
Full textSoetjipto, Hartati, Murda Pradipta, and KH Timotius. "Fatty Acids Composition of Red and Purple Pomegranate (Punica granatum L) Seed Oil." Indonesian Journal of Cancer Chemoprevention 1, no. 2 (2010): 74. http://dx.doi.org/10.14499/indonesianjcanchemoprev1iss2pp74-77.
Full textMohd Said, Farhan, and Nur Fathin Shamirah Daud. "Optimization of Color Fractionation of Monascus Pigment." Journal of Chemical Engineering and Industrial Biotechnology 9, no. 2 (2023): 41–47. http://dx.doi.org/10.15282/jceib.v9i2.9642.
Full textBook chapters on the topic "Acid Red-14"
"So FPTT is associated with two different types of D antigen and three different types of Ce antigens (Table IV). These results suggest that a similar amino acid sequence corresponding to the FPTT antigen is encoded by D genes and by CE genes. Since the genes are highly homologous and proteins very similar, it is possible that similar changes may have occurred. Several mechanisms could be involved: mutation, recombination or gene conversion have been invoked in other blood group systems to explain rare phenotypes. The large number of Rh antigens and their quantitative and qualitative variants will not be easy to explain. Variation in the Rh genes may explain some variants but we know that Rh expression is affected by suppressors unlinked to RH, homozygosity of one unlinked suppressor causes the regulator type of Rhnu|j. Mutation in one of the genes encoding a non-Rh protein required for formation of the Rh protein complex may affect the presentation of some Rh antigens at the cell surface. Rh groups will continue to be clinically and immunologically important until their genetic control is fully understood. Xga AND THE RELATED 12E7 ANTIGEN Unlike Rh antigens, Xga is not clinically significant but was a very valuable marker for studies of the X chromosome. Our interest in Xga and the related 12E7 antigen was rekindled recently by a report of PBDX, a candidate gene for XG [38], and by speculation of the role of 12E7 antigen as an adhesion molecule [39,40]. Xga is red cell specific; in contrast, 12E7 antigen is almost ubiquitous. 12E7 antigen, the MIC2 gene product, has been numbered CD99 at the fifth Leucocyte Workshop and this." In Transfusion Immunology and Medicine. CRC Press, 1995. http://dx.doi.org/10.1201/9781482273441-14.
Full text"Chung and Ohm triterpene alcohols including 4,4'-dimethylsterols, which is germ and aleurone fractions (Table 25). Germs are the substantially higher than those in corn oil and wheat germ richest source of lipids among all cereal grain fractions, oil [126,127,129]. even though they are relatively small fractions of grain Kuroda et al. [128] analyzed SE, S, SG, and ASG of kernels. The weight percentage of germ is 10-14% of corn, bran separately (Table 22). The 4-methylsterols and triter-8-12% of sorghum, 7% of oats, 2-4% of wheat and 1-2% pene alcohols with 4,4'-dimethylsterol were found along of rice kernel weights. with the 4-demethylsterols in SE and S but not in SG or Lipids are unevenly distributed in grain fractions, and ASG. The principal FA components of SE were linoleic lipid distribution differs among grains (Table 25). In corn (58.3%), oleic (30.4%), and palmitic (7.4%) acids, where-kernels, 73-85% of the lipid is distributed in the germ frac-as those of ASG were linoleic (42.5%), palmitic (29.9%), tions [137,138], whereas in rye, triticale, and wheat ker-and oleic (22.7%) acids [97]. The principal 4-demethyl-nels, 34-42% of the lipid is in the germ fraction [78]. The sterols of all flour sterol lipids (SE, S, SG, and ASG) and corn lipid distribution is quite similar despite the genetic bran oil were (3-sitosterol, campesterol, and stigmasterol differences in strains. The H51 is inbred; LG-11 is a three-(Table 22). The principal 4-monomethylsterols of bran oil way cross hybrid forage corn; both the waxy maize and and sterol lipids (SE and S) were gramisterol and citrosta-amylomaize are endosperm mutants. Amylomaize is also a dienol, and the principal 4,4'-dimethylsterols were 24-high-oil strain [9]. Price and Parsons [139] reported that methylenecycloartanol and cycloartenol. the hulless barley (Prilar) and the hulless oat (James) lipids Mahadevappa and Raina [129] reported the total sterol were distributed mainly in the bran-endosperm fractions lipid content as 149 mg in 100 g finger millet including 13 (Table 26). mg SE, 91 mg S, 25 mg SG, and 20 mg ASG. The major Among oat groat fractions, FL and TL were highest in FA, totaling 85-90%, were the same in both esterified the scutellum and BL were highest in embryonic axis sterols, but the proportions varied: palmitic, oleic, and (Table 27). Both red and white proso millet fractions con-linoleic acids comprised 24, 49, and 17% in SE and 43, 36, tained similar lipid contents except for the bran FL con-and 7% in ASG. All flour sterol lipids in finger millet con-tents, which were somewhat higher in the white than those tained 80-84% (3-sitosterol with the reminder being stig-in the red proso millets [33]. masterol [129]. The starch composition influences the lipid content of The 4-demethylsterols compose 87-98% of the total starch. High-amylose barley and corn starch contained sterols in both corn oil and wheat germ oil (Table 23). The higher FFA and LPL contents than waxy and normal types 4-demethylsterol contents were 1441 and 1425 mg in 100 (Table 28). Waxy-type starch contained lower lipid content g of corn oil and wheat germ oil, respectively [130]. The 13-than normal starchs of barley, corn, and rice (Table 28). sitosterol and campesterol are the major 4-demethylsterols in both corn oil and wheat germ oil. The major 4-B. Lipid Compositions in Various monomethylsterols are gramisterol and citrostadienol. In Grain Fractions addition, obtusifoliol is another major component in corn jor 4,4'-dimethylsterols are 24-methylenecy-Since the cereal lipid compositions are too complex to oil. The ma compare for all grains in one section, each will be dis-cloartanol and cycloartenol in corn and wheat germ oils. A cussed separately. substantial amount of 13-amyrin is present in wheat germ oil (Table 23). 1. Barley Long-term storage or heat treatment of flour [132] pro-The average compositions of NL and PL for two varieties, duces sitosterol oxides. The production of sitosterol oxides Kearney (winter type) and Prilar (spring type), are given in was investigated using wheat flour [132]. The 7-hydroxy-Table 29. In barley, like other cereal grains, NL are the ma-sitosterol of wheat flour lipid increased from 25.4 ppm af-jor class of NSTL (Table 3) and over one half of NL are TG ter 2 months storage to 245.0 ppm after storage of 36 (Table 29). The NL also contains 9.8% free sterols, 4.4% months (Table 24). SE, and 5.7% HC [139]. The two major classes of PL are PC and LPC (Table 29). The FA composition varies among lipid classes. The major FA is 18:2 for all classes except for IV. LIPIDS IN STRUCTURAL PARTS PG and PA. The "others" in Table 29 include relatively OF GRAINS small quantities of the other minor FA (12:0, 14:0, 16:1 A. Lipid Contents in Various and 20:0) [142,143]. Grain Fractions The NSL contents and compositions in hulless barley (Prilar) fractions and their FA compositions of NL, GL, Endosperms are the major fractions of all cereal grains, and PL are given in Table 30. The FA composition differs and yet their lipid contents are significantly lower than depending on the structural parts of the barley kernels." In Handbook of Cereal Science and Technology, Revised and Expanded. CRC Press, 2000. http://dx.doi.org/10.1201/9781420027228-45.
Full textConference papers on the topic "Acid Red-14"
Turganbaeva, A. S. "Influence of water concentration on the content of protein and nucleic acids in organs of chick embryos of different ages." In VIII Vserossijskaja konferencija s mezhdunarodnym uchastiem «Mediko-fiziologicheskie problemy jekologii cheloveka». Publishing center of Ulyanovsk State University, 2021. http://dx.doi.org/10.34014/mpphe.2021-191-194.
Full textLane, Ben C. "Diet-responsive blood-indexed risk factor for high myopia." In OSA Annual Meeting. Optica Publishing Group, 1990. http://dx.doi.org/10.1364/oam.1990.tuy24.
Full textBardhan, Pritam, and Manabendra Mandal. "Rhodotorula mucilaginosa R2: A potent oleaginous yeast isolated from traditional fermented food, as a promising platform for the production of lipid-based biofuels, bioactive compounds and other value added products." In 2022 AOCS Annual Meeting & Expo. American Oil Chemists' Society (AOCS), 2022. http://dx.doi.org/10.21748/qbyp3823.
Full textReports on the topic "Acid Red-14"
Hochman, Ayala, Thomas Nash III, and Pamela Padgett. Physiological and Biochemical Characterization of the Effects of Oxidant Air Pollutants, Ozone and Gas-phase Nitric Acid, on Plants and Lichens for their Use as Early Warning Biomonitors of these Air Pollutants. United States Department of Agriculture, 2011. http://dx.doi.org/10.32747/2011.7697115.bard.
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