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BD 362761 Vacutainer®CPT™單核細(xì)胞制備管 CPT制備管
  • 品牌:BD
  • 產(chǎn)地:BD
  • 貨號(hào):361831
  • 發(fā)布日期: 2020-08-13
  • 更新日期: 2024-08-06
產(chǎn)品詳請(qǐng)
產(chǎn)地 BD
品牌 BD
貨號(hào) 361831
用途 CPT制備管
純度 %

BD 362761 Vacutainer®CPT™單核細(xì)胞制備管
BD 362761 Vacutainer®CPT™單核細(xì)胞制備管


    BD 362761 Vacutainer®CPT™單核細(xì)胞制備管


英文名稱:  BD 362761 Vacutainer® CPT™ Mononuclear Cell Preparation Tube - Sodium Citrate (16x125 mm / 8mL)
產(chǎn)品應(yīng)用:  無菌血液收集管,全血收集和單核血細(xì)胞的體外診斷檢驗(yàn)
中國俗稱:  PRP保存管  中國簡稱:  PRP采血管
注冊(cè)品牌:  BD  生產(chǎn)廠家:  BD
訂購貨號(hào):  362761
規(guī)格型號(hào):  60支/箱
保存溫度:  RT
產(chǎn)品種類:  無菌血液收集管,CPT管,PRP管
到貨時(shí)間:  現(xiàn)貨1~5天
產(chǎn)品編碼:  YS0010106

產(chǎn)品中文名稱:BD 362761 Vacutainer®CPT™單核細(xì)胞制備管

產(chǎn)品英文名稱:BD 362761  Vacutainer® CPT™ Mononuclear Cell Preparation Tube - Sodium Citrate  (16x125 mm / 8mL)

      上海華雅思創(chuàng)生物提供的 BD 362761  Vacutainer®CPT™是從全血,其中細(xì)胞分離是在主血液采集試管中進(jìn)行的單核細(xì)胞的分離的完全封閉的系統(tǒng)。這降低了對(duì)單個(gè)核細(xì)胞分離步驟的復(fù)雜性,從而從樣加工*限度地減少可變性。

BD 362761  Vacutainer®CPT™ 也稱CPT™管,是含有緩沖檸檬酸鈉或鈉肝素抗凝,液體密度介質(zhì)和惰性凝膠屏障抽空,無菌血液收集管。它是用于全血收集和單核血細(xì)胞的體外診斷檢驗(yàn)的目的,隨后分離。

全血用標(biāo)準(zhǔn)放血技術(shù)直接吸入到CPT™和在同一管處理。在離心過程中,將凝膠形成的血漿中的單核細(xì)胞和紅細(xì)胞和粒細(xì)胞之間的物理屏障。在血漿中的單核細(xì)胞的分離,濃縮懸浮液然后可以在初級(jí)血液采集管中運(yùn)輸。BD 362761 Vacutainer®CPT™單核細(xì)胞制備管 CPT制備管

BD 362761 Vacutainer® CPT™ is a fully-closed system for separation of  mononuclear cells from whole blood, where cell separation is carried out  in the primary blood collection tube. This decreases the complexity of  steps for mononuclear cell separation, thereby minimizing variability  from sample processing.

CPT™ is an evacuated, sterile blood  collection tube containing buffered sodium citrate or sodium heparin  anticoagulant, liquid density medium and an inert gel barrier. It is  intended for the collection of whole blood and the subsequent separation  of mononuclear blood cells for the purposes of in vitro diagnostic  examination.

Whole blood is drawn directly into the CPT™ using  standard phlebotomy techniques and processed in the same tube. During   centrifugation, the gel forms a physical barrier between the mononuclear  cells in plasma and the erythrocytes and granulocytes. The separated, concentrated suspension of mononuclear cells in plasma can then be   transported in the primary blood collection tube.

BD 362761 Vacutainer®CPT™單核細(xì)胞制備管以下資料供參考:

  1. Azoulay S, Nevers MC, Creminon C, Heripret L, Durant J, et al.  Sensitive Enzyme Immunoassay for Measuring Plasma and Intracellular  Nevirapine Levels in Human Immunodeficiency Virus-Infected Patients.  Antimicrob Agents Chemother 2004;48:104-109.

  2. Baechler E, Battliwalla F, Karypis G, Gaffney P, et al.  Interferon-inducible Gene Expression Signature in Peripheral Blood Cells  of Patients with Severe Lupus. PNAS 2003;100:2610-2615.

  3. Balasuriya U, Snijder E, Heidner H, Zhang J, Zevenhoven-Dobbe  J, Boone J, et al. Development and Characterization of an Infectious  cDNA Clone of the Virulent Bucyrus Strain of Equine Arteritis Virus. J  Gen Virol 2007;88:918-924.

  4. Becher F, Pruvosat A, Schlemmer D, Creminon C, Goujard C, et  al. Significant Levels of Intracellular Stavudine Triphosphate are Found  in HIV-Infected Zidovudine-treated Patients. AIDS 2003;17:555-561.

  5. Bhattacharya S, Tyagi S, Srisuma S, DeMeo D, Shapiro S, et al.  Peripheral Blood Gene Expression Profiles in COPD Subjects. J Clin  Bioinformat 2011;1:1-12.

  6. Colombo S, Beguin A, Telenti A, Biollaz J, Buclin T, et al.  Intracellular Measurements of anti-HIV Drugs Indinavir, Amprenavir,  Saquinavir, Nelfinavir, Lipinavir, Atazanavir, Efavirenz and Nevirapine  in Peripheral Blood Mononuclear Cells by Liquid Chromatography Coupled  to Tandem Mass Spectrometry. J Chromatograph B 2005;819:259-276.

  7. Cronin AJ, Aucutt-Walter NM, Budinetz T, Bonafide CP,  DiVittore, NA, et al. Low Dose Remifentanil Infusion Does Not Impair  Natural Killer Cell Function in Healthy Volunteers. Br J Anaesth  2003;91:805-809.

  8. Ehrhardt M, Mock M, Haefeli W, Mikus G, Burhenne J. Monitoring  of Lopinavir and Ritonavir in Peripheral Blood Mononuclear Cells,  Plasma, and Ultrafiltrate using a Selective and Highly Sensitive  LC/MS/MS Assay. J Chromatograph B 2007;850:249-258.

  9. Fischer M, Huber W, Kalivroussis A, Ott P, Opravil M, et al.   Highly Sensitive Methods for Quantitation of Human Immunodeficiency  Virus Type 1 RNA from Plasma, Cells and Tissues. J Clin Microbiol  1999;37:1260-1264.

  10. Green LJ, Marker P, Ray C, Cook CA, Jaken S, et al.  Development and Validation of a Drug Activity Biomarker that Shows Target Inhibition in Cancer Patients Receiving Enzastaurin, a Novel   Protein Kinase C-B Inhibitor. Clin Cancer Res 2006;12:3408-3415.

  11. Holodniy M, Mole L, Yen-Lieberman B, Margolis D, Starkey C, et  al. Comparative stabilities of Quantitative Human Immunodeficiency  Virus RNA in Plasma from Samples Collected in Vacutainer CPT, Vacutainer  PPT and Standard Vacutainer Tubes. J Clin Microbiol 1995;33:1562-1566.

  12. Hughes A, Mattison J, Western L, Powderly J, et al. Microtube  Device for Selectin-Mediated Capture of Viable Circulating Tumor Cells  from Blood. Clin Chem 2012;58:846-853.

  13. Katial RK, Brandt BL, Moran EE, Marks S, Agnello V, Zollinger  W. Immunogenicity and Safety Testing of a Group B Intranasal  Meningococcal Native Outer Membrane Vesicle Vaccine. Infect Immun  2002;70:702-707.

  14. Mahony J, Chong S, Coombes B, Smieja M, Petrich A. Analytical  Sensitivity, Reproducibility of Results, and Clinical Performance of  Five PCR Assays for Detecting Chlamydia Pneumoniae DNA in Peripheral  Blood Mononuclear Cells. J Clin Microbiol 2000;38:2622-2627.

  15. Mole L, Margolis D, Carroll R, Todd J, Holodniy J. Stabilities  of Quantitative Plasma Culture for Human Immunodeficiency Virus, RNA,  and p24 Antigen from Samples Collected in Vacutainer CPT and Standard  Vacutainer Tubes. J Clin Microbiol 1994;32:2212-2215.

  16. Pierini M, Dozza B, Lucarelli E, Tazzari P, et al. Efficient  Isolation and Enrichment of Mesenchymal Stem Cells from Bone Marrow.  Cytotherapy 2012;14:686-693.

  17. Ramanathan R, Egorin M, Eiseman J, Ramalingam S, Friedland D,  Agarwala S, et al. Phase I and Pharmacodynamic Study of   17-(Allylamino)-17-Demethoxygeldanamycin in Adult Patients with   Refractory Advanced Cancers. Clin Cancer Res 2007;13:1769-1774.

  18. Rouzes A, Berthoin K, Zuereb F, Djabarouti S, Pellegrin I, et  al. Simultaneous Determination of the Antiretroviral Agents: Amprenavir,  Lipinavir, Ritonavir, Saquinavir and Efavirenz in Human Peripheral  Blood Mononuclear Cells by High Performance Liquid Chromatography—Mass  Spectrometry. J Chromatograph B 2004;813:209-216.

  19. Ruitenberg J, Mulder C, Maino V, Landay A, Ghanekar S.  Vacutainer CPT and Ficoll Density Gradient Separation Perform  Equivalently in Maintaining the Quality and Function of PBMC from HIV  Seropositive Blood Samples. BMC Immunol 2006;7:1-8.

  20. Schlenke P, Klüter H, Müller-Steinhardt M, Hammers HJ,  Borchert K, Bein G. Evaluation of a Novel Mononuclear Cell Isolation  Procedure for Serological HLA Typing. Clin Diagn Lab Immunol 1998;5:808-813.

  21. Shariat S, Gottenger E, Nguyen C, Song W, Kattan M, et al.  Preoperative Blood Reverse Transcriptase-PCR Assays for   Prostate-Specific Antigen and Human Glandular Kallikrein for Prediction of Prostate Cancer Progression after Radical Prostatectomy. Cancer   Research 2002;62:5974-5979.

  22. Slawin K, Shariat S, Nguyen C, Leventis A, Song W, et al.  Detection of Metastatic Prostate Cancer using a Splice Variant-Specific  Reverse Transcriptase-Polymerase Chain Reaction Assay for Human  Glandular Kallikrein. Cancer Research 2000;60:7142-7148.

 

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