{"id":855,"date":"2017-03-13T15:04:41","date_gmt":"2017-03-13T14:04:41","guid":{"rendered":"http:\/\/www.bluelabservice.it\/?page_id=855"},"modified":"2017-11-03T12:43:26","modified_gmt":"2017-11-03T11:43:26","slug":"chimica-clinica","status":"publish","type":"page","link":"https:\/\/www.bluelabservice.it\/en\/chimica-clinica\/dirui-barcoded\/chimica-clinica\/","title":{"rendered":"Clinical chemistry"},"content":{"rendered":"

<\/p>\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n
<\/td>\n<\/tr>\n
<\/td>\nRef<\/strong><\/td>\nDescription <\/strong><\/td>\nPack <\/b><\/td>\n<\/td>\n<\/td>\n<\/td>\n<\/tr>\n
<\/td>\n030063<\/strong><\/td>\nTotal bile acids<\/b><\/td>\n5×10; 1×13 ml<\/strong><\/td>\n<\/td>\n<\/td>\n<\/td>\n<\/tr>\n
<\/td>\n<\/td>\nEnzymatic colorimetric method with NBT. Absorption 546 nm. Bi-reactive (Fixed-time in 5 min). Sample report\/Solution R1\/Reagent 2: 1\/2\/0.5. Linearity 200 <\/em>mmol\/l. Standard kit<\/em><\/td>\n<\/td>\n<\/tr>\n
<\/td>\n890250<\/strong><\/td>\nUric acid <\/b><\/td>\n5×50 ml<\/strong><\/td>\n<\/td>\n<\/td>\n<\/td>\n<\/tr>\n
<\/td>\n<\/td>\n Enzymatic colorimetric method Trinder. Absorption 550 nm. <\/em>Mono-reactive (End point in 10 min). Sample report\/ R1: 1\/40. Linearity: 20 mg\/dl.<\/em><\/p>\n

 <\/td>\n

<\/td>\n<\/tr>\n
<\/td>\n1310300<\/strong><\/td>\nAlbumin<\/strong><\/td>\n4×75 ml<\/strong><\/td>\n<\/td>\n<\/td>\n<\/td>\n<\/tr>\n
<\/td>\n<\/td>\nColorimetric method using bromocresol Green. Absorption 630 nm. Mono-reactive. Sample report \/R1: 1\/300. Linearity: to 6 g\/dl <\/em><\/p>\n

 <\/td>\n

<\/td>\n<\/tr>\n
<\/td>\n900100<\/strong><\/td>\nAldolase <\/strong><\/td>\n5×20 ml<\/strong><\/td>\n<\/td>\n<\/td>\n<\/td>\n<\/tr>\n
<\/td>\n<\/td>\nKinetic method U.V. Aldolase in Serum and plasma. Absorption 340 nm. Tri-reactive: 1 liofilo reagent. Sample report \/Solution R1\/R2\/R3: 1\/12.5\/0.25\/0.05. Linearity: 30 UI\/l.<\/em><\/p>\n

 <\/td>\n

<\/td>\n<\/tr>\n
<\/td>\n270100<\/strong><\/td>\nAlpha amylase<\/strong><\/td>\n2×50 ml<\/strong><\/td>\n<\/td>\n<\/td>\n<\/td>\n<\/tr>\n
<\/td>\n<\/td>\nEnzymatic colorimetric method to CNPG3<\/sub> in the serum, in the plasma and in the urine. Absorption 405 nm. Mono-reactive. Sample report \/R1: 1\/40. Linearity: 1500 U\/l <\/em><\/p>\n

 <\/td>\n

<\/td>\n<\/tr>\n
<\/td>\n910100<\/strong><\/td>\nAmmonia Ultra<\/strong><\/td>\n3×20 ml<\/strong><\/td>\n<\/td>\n<\/td>\n<\/td>\n<\/tr>\n
<\/td>\n<\/td>\nUV Enzymatic kinetic method ( GLDH). Absorption 340 nm. Mono-reactive. Sample report \/ R1: 1\/11. Linearity: 1700 \u00b5g\/dl. Standard kit. <\/em><\/p>\n

 <\/td>\n

<\/td>\n<\/tr>\n
<\/td>\n520250<\/strong><\/td>\nDirect bilirubin <\/b><\/td>\n4×75; 2×5 ml<\/strong><\/td>\n<\/td>\n<\/td>\n<\/td>\n<\/tr>\n
<\/td>\n<\/td>\nColorimetric method DMSO. Absorption 555 nm. Bi-reactive with sample white (End point in 5 min). Sample report \/Solution\/Reagent 2: 1\/15\/0.5. Mono-reactive without sample white. Sample report \/Solution R1: 1\/15. Linearity: 20 mg\/dl.<\/em><\/p>\n

 <\/td>\n

<\/td>\n<\/tr>\n
<\/td>\n280250<\/strong><\/td>\nTotal bilirubin<\/b><\/td>\n4×75; 2×5 ml<\/strong><\/td>\n<\/td>\n<\/td>\n<\/td>\n<\/tr>\n
<\/td>\n<\/td>\nColorimetric method . Absorption 555 nm. End point in 5 min. Bi-reactive with sample white . Sample report \/R1\/R2: 1\/15\/0.5. Mono-reactive without sample white. Sample report \/Solution: 1\/15. Linearity: 20 mg\/dl.<\/em><\/p>\n

 <\/td>\n

<\/td>\n<\/tr>\n
<\/td>\n600250<\/strong><\/td>\nCalcium arsenate III<\/strong><\/td>\n4×62.5 ml<\/strong><\/td>\n<\/td>\n<\/td>\n<\/td>\n<\/tr>\n
<\/td>\n<\/td>\nColorimetric method to Arsenazo. Absorption 660 nm. <\/em>Mono-reactive, end point in 5 min. Sample report \/R1: 1\/100. Linearity: 20 mg\/dl <\/em><\/p>\n

 <\/p>\n

 <\/td>\n

<\/td>\n<\/tr>\n
<\/td>\n1010060<\/strong><\/td>\nCk-Mb<\/strong><\/td>\n1×20 + 1×5 ml<\/strong><\/td>\n<\/td>\n<\/td>\n<\/td>\n<\/tr>\n
<\/td>\n<\/td>\nKinetic method U.V . Absorption 340 nm. Bi-reactive. Sample report \/R1\/R2: 1\/20\/5. Linearity: 600 U\/l <\/em><\/p>\n

 <\/p>\n

 <\/td>\n

<\/td>\n<\/tr>\n
<\/td>\n550250<\/strong><\/td>\nCk-Nac<\/strong><\/td>\n5×50 ml<\/strong><\/td>\n<\/td>\n<\/td>\n<\/td>\n<\/tr>\n
<\/td>\n<\/td>\nKinetic method UV for the determination of Creatine Kinase in serum and plasma. Absorption 340 nm. Bi-reactive . Sample report \/R1\/R2: 1\/32\/8. Linearity: 1600 Ul\/L.<\/em><\/td>\n<\/td>\n<\/tr>\n
<\/td>\n750300<\/strong><\/td>\nChlorides <\/strong><\/td>\n4×75 ml<\/strong><\/td>\n<\/td>\n<\/td>\n<\/td>\n<\/tr>\n
<\/td>\n<\/td>\nDirect colorimetric method of Chlorides in biological fluids. Absorption 480 nm. Mono-reactive (end point in 5 min) \/R1: 1\/100. Linearity: 130 mEq\/l. <\/em><\/p>\n

 <\/td>\n

<\/td>\n<\/tr>\n
<\/td>\n770200-180<\/strong><\/td>\nDirect HDL cholesterol<\/strong><\/td>\n3×45 + 1×45 ml<\/strong><\/td>\n<\/td>\n<\/td>\n<\/td>\n<\/tr>\n
<\/td>\n<\/td>\nDirect method without precipitation for the determination of HDL cholesterol. Reading 600 nm. Bi-reactive End point in 5 min. Sample report 1\/75\/\/R1\/R2:25. Linearity: 180 mg\/dl.<\/em><\/p>\n

 <\/td>\n

<\/td>\n<\/tr>\n
<\/td>\n1300080<\/strong><\/td>\nDirect LDL Cholesterol<\/strong><\/td>\n1×30 + 1×10 ml<\/strong><\/td>\n<\/td>\n<\/td>\n<\/td>\n<\/tr>\n
<\/td>\n<\/td>\nDirect method without precipitation for the determination of LDL cholesterol. Absorption 600 nm. Bi-reactive. End point in 5 min. Sample report 1\/75\/\/R1\/R2:25. Linearity: 1000 mg\/dl.<\/em><\/p>\n

 <\/td>\n

<\/td>\n<\/tr>\n
<\/td>\n540300<\/strong><\/td>\nTotal Cholesterol<\/b><\/td>\n4×75 ml<\/strong><\/td>\n<\/td>\n<\/td>\n<\/td>\n<\/tr>\n
<\/td>\n<\/td>\nTrinder colorimetric enzymatic method of cholesterol of the serum and plasma. Absorption 510 nm. Monoreagent, end point in 5 min. Sample report \/R1:1\/100. Linearity: 700 mg\/dl<\/em><\/p>\n

\u00a0<\/em><\/td>\n

<\/td>\n<\/tr>\n
<\/td>\n10250<\/strong><\/td>\nCholinesterase<\/strong><\/td>\n5×50 ml<\/strong><\/td>\n<\/td>\n<\/td>\n<\/td>\n<\/tr>\n
<\/td>\n<\/td>\nDescending kinetic method for the determination of Cholinesterase in the serum and plasma. 405 nm reading. Bi-reactive . Sample report\/R1\/R2:1\/40\/10. Linearity: 12000 U\/L<\/em><\/p>\n

\u00a0<\/em><\/td>\n

<\/td>\n<\/tr>\n
<\/td>\n550300<\/strong><\/td>\nCreatinine<\/strong><\/td>\n2×75 + 2×75 ml<\/strong><\/td>\n<\/td>\n<\/td>\n<\/td>\n<\/tr>\n
<\/td>\n<\/td>\nCreatinine colorimetric method in biological fluids without Deproteinization. Absorption 510 nm. BI-reactive, Fixed-time. Sample report \/R1\/R2:1\/20\/20. Linearity: 25 mg\/dl.<\/em><\/p>\n

 <\/td>\n

<\/td>\n<\/tr>\n
<\/td>\nBLS1210<\/strong><\/td>\nMonoreagent Creatine<\/b><\/td>\n4×75 ml<\/strong><\/td>\n<\/td>\n<\/td>\n<\/td>\n<\/tr>\n
<\/td>\n<\/td>\nCreatinine colorimetric method in biological fluids without Deproteinization. Absorption 510 nm. Monoreagent, Fixed-time. Sample report\/R1:1\/40. Linearity: 25 mg\/dl<\/em><\/p>\n

\u00a0<\/em><\/td>\n

<\/td>\n<\/tr>\n
<\/td>\n1320010<\/strong><\/td>\nDIbucaine<\/strong><\/td>\n2×10 ml<\/strong><\/td>\n<\/td>\n<\/td>\n<\/td>\n<\/tr>\n
<\/td>\n<\/td>\nDescending kinetic method for quantitative determination of Dibucaine ointment 1% number. Absorption 405 nm . Monoreagent. Sample report \/R1\/R2:1\/40\/10. Linearity: 12000 U\/L. To use together with the Colinestrasi kit (Ref 10250).<\/em><\/p>\n

\u00a0<\/em><\/td>\n

<\/td>\n<\/tr>\n
<\/td>\n570250<\/strong><\/td>\nIron Ferene<\/b><\/td>\n3×66.67 + 1×50 ml<\/strong><\/td>\n<\/td>\n<\/td>\n<\/td>\n<\/tr>\n
<\/td>\n<\/td>\nThe method for determination of serum iron Ferene. Absorption 578 nm. Bi-reactive, end point. Sample report\/1\/4\/1 R1\/R2:. Linearity: 600 \u00b5 g\/dl.<\/em><\/p>\n

\u00a0<\/em><\/td>\n

<\/td>\n<\/tr>\n
<\/td>\n3-258<\/strong><\/td>\nIron Ferene<\/b><\/td>\n5×50 + 1×50 ml<\/strong><\/td>\n<\/td>\n<\/td>\n<\/td>\n<\/tr>\n
<\/td>\n<\/td>\nThe method for determination of serum iron Ferene. Absorption 550 nm. Bireactive (End point in 10 min). Sample report: 8\/1\/\/R1\/R2 2. Linearity: 1000 \u00b5 g\/dl.<\/em><\/p>\n

 <\/td>\n

<\/td>\n<\/tr>\n
<\/td>\n1330057<\/strong><\/td>\nTotal Acid phosphatase<\/strong><\/td>\n19×2 ml<\/strong><\/td>\n<\/td>\n<\/td>\n<\/td>\n<\/tr>\n
<\/td>\n<\/td>\nColorimetric method-Naftilfosfato. Absorption 405 nm . Bireactive, kinetic. 1\/10\/R1: sample report for total acid phosphatase. Sample report: 1\/10\/R1\/R2\/0.1 for prostatic fraction. Linearity: 150 IU\/l. The working solution is prepared from lyophilized: stability 2 R1 days at 2-8\u00b0 c.<\/em><\/td>\n<\/td>\n<\/tr>\n
<\/td>\n580250<\/strong><\/td>\nAlkaline Phosphatase<\/b><\/td>\n5×50 ml<\/strong><\/td>\n<\/td>\n<\/td>\n<\/td>\n<\/tr>\n
<\/td>\n<\/td>\nKinetic method for the determination of alkaline phosphatase in serum and plasma based on the recommendations of the DGKC. Absorption 405 nm . Bireactive. Sample report\/R1\/R2:1\/40\/10. Linearity: 2000 U\/l.<\/em><\/td>\n<\/td>\n<\/tr>\n
<\/td>\n590300<\/strong><\/td>\nPhosphorus <\/b><\/td>\n4×75 ml<\/strong><\/td>\n<\/td>\n<\/td>\n<\/td>\n<\/tr>\n
<\/td>\n<\/td>\nDirect colorimetric method for the determination of inorganic phosphorus on serum samples. Absorption 340 nm. Monoreagent, end point in 5 min. Sample report\/R1:1\/100. Linearity: 20 mg\/dl.<\/em><\/td>\n<\/td>\n<\/tr>\n
<\/td>\n240250<\/strong><\/td>\nGamma GT<\/strong><\/td>\n5×50 ml<\/strong><\/td>\n<\/td>\n<\/td>\n<\/td>\n<\/tr>\n
<\/td>\n<\/td>\nKinetic method for the determination of Gamma-glutamyl-transferase in serum and plasma. Absorption 405 nm. Bi-reactive. Sample report\/R1\/R2:1\/16\/4. Linearity: 1200 IU\/l.<\/em><\/p>\n

 <\/td>\n

<\/td>\n<\/tr>\n
<\/td>\n610300<\/strong><\/td>\nGlucose<\/strong><\/td>\n4×75 ml<\/strong><\/td>\n<\/td>\n<\/td>\n<\/td>\n<\/tr>\n
<\/td>\n<\/td>\nColorimetric method for the determination of Glucose in serum and plasma. Absorption 510 nm. Monoreagent, End point in 5 min. Sample report\/R1:1\/100. Linearity: 500 mg\/dl.<\/em><\/td>\n<\/td>\n<\/tr>\n
<\/td>\n100250<\/strong><\/td>\nGot<\/strong> (Ast<\/strong>)<\/strong><\/td>\n 5×50 ml<\/strong><\/td>\n<\/td>\n<\/td>\n<\/td>\n<\/tr>\n
<\/td>\n<\/td>\nKinetic method for the determination of aspartate aminotransferase in serum and plasma according to recommendation of the IFCC. Absorption 340 nm. Bi-reactive. Sample report\/R1\/R2:1\/8\/2. Linearity: 440 mg\/dl.<\/em><\/p>\n

 <\/td>\n

<\/td>\n<\/tr>\n
<\/td>\n120250<\/strong><\/td>\nGpt<\/strong> (Alt<\/strong>)<\/strong><\/td>\n 5×50 ml<\/strong><\/td>\n<\/td>\n<\/td>\n<\/td>\n<\/tr>\n
<\/td>\n<\/td>\nKinetic method for the determination of alanine aminotransferase in serum and plasma according to recommendation of the IFCC. Absorption 340 nm. Bi-reactive. Sample report\/R1\/R2:1\/8\/2. Linearity: 440 mg\/dl.<\/em><\/p>\n

 <\/td>\n

<\/td>\n<\/tr>\n
<\/td>\n230250<\/strong><\/td>\nLdh<\/strong><\/td>\n5×50 ml<\/strong><\/td>\n<\/td>\n<\/td>\n<\/td>\n<\/tr>\n
<\/td>\n<\/td>\nKinetic method for the determination of lactate dehydrogenase in serum and plasma based on recommendation of the DGKC. Absorption 340 nm. Bireactive. Sample report\/R1:\/R2:1\/40\/10. Linearity: 800 U\/l.<\/em><\/p>\n

 <\/td>\n

<\/td>\n<\/tr>\n
<\/td>\n1340048<\/strong><\/td>\nLipase<\/strong><\/td>\n1×40 + 1×8 ml<\/strong><\/td>\n<\/td>\n<\/td>\n<\/td>\n<\/tr>\n
<\/td>\n<\/td>\nDetermination of pancreatic lipase in human serum and plasma. Absorption 570 or 580 nm. BI-reactive, kinetic method. Sample report\/R1\/R2:1\/100\/50. Linearity: 400 IU\/l. winder calibrator.<\/em><\/td>\n<\/td>\n<\/tr>\n
<\/td>\n700300<\/strong><\/td>\nMagnesium <\/strong><\/td>\n4×75 ml<\/strong><\/td>\n<\/td>\n<\/td>\n<\/td>\n<\/tr>\n
<\/td>\n<\/td>\nColorimetric method for the determination of the xylidyl bleu magnesium in serum. Reading 520 nm. Monoreagent, end point in 3 min. Sample report\/R1:1\/100. Linearity: 5 mg\/dl.<\/em><\/p>\n

 <\/td>\n

<\/td>\n<\/tr>\n
<\/td>\n650300<\/strong><\/td>\nTotal Protein <\/b><\/td>\n4×75 ml<\/strong><\/td>\n<\/td>\n<\/td>\n<\/td>\n<\/tr>\n
<\/td>\n<\/td>\nThe colorimetric method for the determination of total protein biuret in serum and plasma. Absorption 540 nm. Monoreagent, end point in 10 minutes. Sample report\/R1:1\/100. Linearity: 10 g\/dL.<\/em><\/p>\n

\u00a0<\/em><\/td>\n

<\/td>\n<\/tr>\n
<\/td>\n1920300<\/strong><\/td>\nTotal Protein (Urine e Liquor)<\/strong><\/td>\n4×75 ml<\/strong><\/td>\n<\/td>\n<\/td>\n<\/td>\n<\/tr>\n
<\/td>\n<\/td>\nColorimetric method for the determination of protein in urine and CSF. Absorption 600 nm. Monoreagent (End point in 10 min). Sample report\/R1:1\/50. Linearity: 200 mg\/dl.<\/em><\/p>\n

 <\/td>\n

<\/td>\n<\/tr>\n
<\/td>\n340300<\/strong><\/td>\nTriglycerides<\/b><\/td>\n 4×75 ml<\/strong><\/td>\n<\/td>\n<\/td>\n<\/td>\n<\/tr>\n
<\/td>\n<\/td>\nColorimetric method for the determination of Trinder triglycerides in serum and plasma. Absorption 546 nm. Monoreagent, end point in 5 minutes. Sample report \/R1:1\/100\/. Linearity: 1000 mg\/dl.<\/em><\/td>\n<\/td>\n<\/tr>\n
<\/td>\n540250<\/strong><\/td>\nUrea<\/strong><\/td>\n5×50 ml<\/strong><\/td>\n<\/td>\n<\/td>\n<\/td>\n<\/tr>\n
<\/td>\n<\/td>\nKinetic method for the determination of Urea in serum, plasma or urine. Absorption of 340 nm. Sample report \/1\/80\/20\/R2:R1: Linearity:350 mg\/dl <\/i><\/p>\n

 <\/td>\n

<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n

 <\/p>","protected":false},"excerpt":{"rendered":"

Ref Description Pack 030063 Total bile acids 5×10; 1×13 ml Enzymatic colorimetric method with NBT. Absorption 546 nm. Bi-reactive (Fixed-time […]<\/p>\n","protected":false},"author":3,"featured_media":0,"parent":77,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"site-sidebar-layout":"default","site-content-layout":"","ast-site-content-layout":"default","site-content-style":"default","site-sidebar-style":"default","ast-global-header-display":"","ast-banner-title-visibility":"","ast-main-header-display":"","ast-hfb-above-header-display":"","ast-hfb-below-header-display":"","ast-hfb-mobile-header-display":"","site-post-title":"","ast-breadcrumbs-content":"","ast-featured-img":"","footer-sml-layout":"","ast-disable-related-posts":"","theme-transparent-header-meta":"","adv-header-id-meta":"","stick-header-meta":"","header-above-stick-meta":"","header-main-stick-meta":"","header-below-stick-meta":"","astra-migrate-meta-layouts":"default","ast-page-background-enabled":"default","ast-page-background-meta":{"desktop":{"background-color":"var(--ast-global-color-5)","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""},"tablet":{"background-color":"","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""},"mobile":{"background-color":"","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""}},"ast-content-background-meta":{"desktop":{"background-color":"var(--ast-global-color-4)","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""},"tablet":{"background-color":"var(--ast-global-color-4)","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""},"mobile":{"background-color":"var(--ast-global-color-4)","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""}},"footnotes":""},"class_list":["post-855","page","type-page","status-publish","hentry"],"yoast_head":"\nClinical chemistry -<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/www.bluelabservice.it\/en\/chimica-clinica\/dirui-barcoded\/chimica-clinica\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Clinical chemistry -\" \/>\n<meta property=\"og:description\" content=\"Ref Description Pack 030063 Total bile acids 5×10; 1×13 ml Enzymatic colorimetric method with NBT. 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Absorption 546 nm. 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