Journal of bioluminescence and chemiluminescence最新文献_第2页

The Fireflies and Luminous Insects 萤火虫和发光的昆虫

Journal of bioluminescence and chemiluminescence Pub Date : 2006-09-01 DOI: 10.1142/9789812773647_0001

O. Shimomura

引用次数: 3

Dinoflagellates and Other Protozoa 鞭毛虫和其他原生动物

Journal of bioluminescence and chemiluminescence Pub Date : 2006-09-01 DOI: 10.1142/9789812773647_0008

O. Shimomura

引用次数: 1

The Jellyfish Aequorea and Other Luminous Coelenterates 水母和其他发光腔肠动物

Journal of bioluminescence and chemiluminescence Pub Date : 2006-09-01 DOI: 10.1142/9789812773647_0004

O. Shimomura

引用次数: 6

Other Luminous Organisms 其他发光生物

Journal of bioluminescence and chemiluminescence Pub Date : 2006-09-01 DOI: 10.1142/9789812773647_0010

O. Shimomura

引用次数: 0

Immobilization of luciferase from a firefly lantern extract on glass strips as an alternative strategy for luminescent detection of ATP. 萤光灯提取物的荧光素酶固定在玻璃条上作为发光检测ATP的替代策略。

Journal of bioluminescence and chemiluminescence Pub Date : 1998-11-01 DOI: 10.1002/(SICI)1099-1271(199811/12)13:6<371::AID-BIO510>3.0.CO;2-#

A R Ribeiro, R M Santos, L M Rosário, M H Gil

{"title":"Immobilization of luciferase from a firefly lantern extract on glass strips as an alternative strategy for luminescent detection of ATP.","authors":"A R Ribeiro, R M Santos, L M Rosário, M H Gil","doi":"10.1002/(SICI)1099-1271(199811/12)13:6<371::AID-BIO510>3.0.CO;2-#","DOIUrl":"https://doi.org/10.1002/(SICI)1099-1271(199811/12)13:6<371::AID-BIO510>3.0.CO;2-#","url":null,"abstract":"The bioluminescent reaction catalysed by firefly luciferase has become widely established as an outstanding analytical system for assay of ATP. When used in solution, luciferase is unstable and cannot be re-used, a problem that can be partially circumvented by immobilizing the enzyme on solid substrates. Transparent glass is especially advantageous over alternative immobilizing matrices, since it allows most of the emitted photons to be detected. We report a new method for luciferase immobilization on glass which does not require prior silanization and glutaraldehyde activation, thus saving preparation time and minimizing enzyme inactivation. Our method is based on the co-immobilization by adsorption of luciferase (from a firefly lantern extract) and poly-L-lysine (PL) on non-porous glass strips. Luciferase immobilized in this way exhibits minimal variations in intersample activity, high sensitivity for ATP detection (linear luminescence responses down to 50 nmol/L) and good stability (full activity for at least 60 days when stored at -80 degrees C). PL-mediated immobilization of luciferase on glass strips provides an attractive strategy for the design of specific ATP biosensors, with potential in industry, environmental screening, medicine and biological research.","PeriodicalId":15068,"journal":{"name":"Journal of bioluminescence and chemiluminescence","volume":"13 6","pages":"371-8"},"PeriodicalIF":0.0,"publicationDate":"1998-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"20831900","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 33

Bioluminescence and chemiluminescence literature. Green fluorescent protein. 生物发光和化学发光文献。绿色荧光蛋白。

Journal of bioluminescence and chemiluminescence Pub Date : 1997-03-01

L J Kricka, P E Stanley

引用次数: 0

Expression of the Renilla reniformis luciferase gene in mammalian cells. Renilla reniformis荧光素酶基因在哺乳动物细胞中的表达。

Journal of bioluminescence and chemiluminescence Pub Date : 1996-01-01 DOI: 10.1002/(SICI)1099-1271(199601)11:1<31::AID-BIO398>3.0.CO;2-M

W W Lorenz, M J Cormier, D J O'Kane, D Hua, A A Escher, A A Szalay

引用次数: 90

Effect of enhancers on the pyridopyridazine-peroxide-HRP reaction. 增强剂对吡啶吡啶-过氧化物- hrp反应的影响。

Journal of bioluminescence and chemiluminescence Pub Date : 1996-01-01 DOI: 10.1002/(SICI)1099-1271(199601)11:1<1::AID-BIO389>3.0.CO;2-2

X Ji, K Kondo, Y Aramaki, L J Kricka

{"title":"Effect of enhancers on the pyridopyridazine-peroxide-HRP reaction.","authors":"X Ji, K Kondo, Y Aramaki, L J Kricka","doi":"10.1002/(SICI)1099-1271(199601)11:1<1::AID-BIO389>3.0.CO;2-2","DOIUrl":"https://doi.org/10.1002/(SICI)1099-1271(199601)11:1<1::AID-BIO389>3.0.CO;2-2","url":null,"abstract":"4-Substituted phenyl boronic acids (e.g., 4-iodo, 4-bromo, 4-phenyl) are effective enhancers of the horseradish peroxidase (Type VIA) catalysed chemiluminescent oxidation of various pyrido[3,4-d]pyridazine-1,4(2H,3H)dione derivatives. The most effective combination was 4-biphenylboronic acid and 8-amino-5-chloro-7-phenylpyrido[3,4-d]- pyridazine-1,4(2H,3H)dione. Generally, the intensity of light emission in the presence of peroxidase was higher with the pyridopyridazines than with sodium luminol. However, the blank light emission was much lower with sodium luminol than with the pyridopyridazines. A synergistic enhancement phenomenon was demonstrated for the combination of a 4-iodophenol and a 4-biphenylboronic acid enhancer with 8-amino-5-chloro-7-phenylpyrido[3,4-d]pyridazine-1,4(2H,3H) dione. The combination of these two enhancers produced a light emission intensity in an assay for 5 fmol of peroxidase that was 25% higher than expected from the sum of the individual light intensities.","PeriodicalId":15068,"journal":{"name":"Journal of bioluminescence and chemiluminescence","volume":"11 1","pages":"1-7"},"PeriodicalIF":0.0,"publicationDate":"1996-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/(SICI)1099-1271(199601)11:1<1::AID-BIO389>3.0.CO;2-2","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"19660569","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 1

Chemiluminescence emission during reactions between superoxide and selected aliphatic and aromatic halocarbons in aprotic media. 在非质子介质中超氧化物与选定的脂肪族和芳香族卤代烃反应时的化学发光发射。

Journal of bioluminescence and chemiluminescence Pub Date : 1996-01-01 DOI: 10.1002/(SICI)1099-1271(199601)11:1<9::AID-BIO396>3.0.CO;2-N

A R Shoaf, A U Shaikh, J H Ford, W C Carlson, R H Steele

{"title":"Chemiluminescence emission during reactions between superoxide and selected aliphatic and aromatic halocarbons in aprotic media.","authors":"A R Shoaf, A U Shaikh, J H Ford, W C Carlson, R H Steele","doi":"10.1002/(SICI)1099-1271(199601)11:1<9::AID-BIO396>3.0.CO;2-N","DOIUrl":"https://doi.org/10.1002/(SICI)1099-1271(199601)11:1<9::AID-BIO396>3.0.CO;2-N","url":null,"abstract":"The reactions between superoxide free radical anion (.O2-) with the halocarbons CCl4. CHCl3, BrCH2CH2Br(EDB), decachlora-biphenyl (DCBP), and 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) in dimethyl sulphoxide (DMSO) results in the emission of chemiluminescence (CL). The chemiluminescence reactions are characterized as having biphasic second order kinetics, CL wavelengths between 350 nm and 650 nm, and exhibiting perturbation by chemicals reactive with singlet oxygen. These data suggest that singlet oxygen species are the excited state responsible for the light emissions. Polarographic studies confirm .O2- consumption and halide release in the reactions, while gas liquid chromatography and NBT reduction demonstrate the decomposition of the halocarbons into products. A chemiluminescent reaction mechanism is proposed involving reductive dehalogenation of the halocarbons and the generation of singlet oxygen. The significance of singlet oxygen generation is discussed with respect to a general mechanism for explaining the rapid initiation of lipid peroxidative membrane damage in halocarbon toxigenicity in animal and plant tissues.","PeriodicalId":15068,"journal":{"name":"Journal of bioluminescence and chemiluminescence","volume":"11 1","pages":"9-22"},"PeriodicalIF":0.0,"publicationDate":"1996-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/(SICI)1099-1271(199601)11:1<9::AID-BIO396>3.0.CO;2-N","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"19661225","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 0

Competitive chemiluminescent immunoassay for estradiol using an N-functionalized acridinium ester. 利用n功能化吖啶酯对雌二醇进行竞争性化学发光免疫分析。

Journal of bioluminescence and chemiluminescence Pub Date : 1996-01-01 DOI: 10.1002/(SICI)1099-1271(199601)11:1<23::AID-BIO400>3.0.CO;2-A

H Sato, H Mochizuki, Y Tomita, T Izako, N Sato, T Kanamori

引用次数: 9