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支原体Pneumoniae (MP) - IgG卡式磁带

支原体Pneumoniae (MP) - IgG卡式磁带
送询问
产品编码: 37
品牌: Bioneovan
价格和数量
  • 最低订单量
  • 1000
  • 计量单位
  • 片断或片断
  • 价格
  • 0.9 USD ($)
产品说明

意欲的用途

这测试成套工具用于定性地查出支原体pneumoniae (MP) - IgG抗体的存在当前在清液或血浆样品和使用作为MP传染一种辅助诊断试剂在诊所或实验室。 MP是导致主要非典型肺炎和其他呼吸传染病的共同的致病性微生物。 除此之外,它可能导致其他严肃的复杂化。 MP传染普遍,并且它可能造成咽炎、支气管炎、肺脓肿、扁桃腺炎、肺bullae和pleurisy和多系统损伤。 辨认是不容易的肺炎是由MP、病毒、细菌和其他病原生物传染造成的。 MP传染的治疗是与其他细菌或病毒感染不同。 在传染以后, MPIgM以前出现它然后减少与MPIgG滴定量的增长的水平。 另外, IgM抗体正面一般是微弱的在第一传染; 因此, IgM阴性不意味MP传染inexistence。 IgG抗体侦查是根本和必要的。

测试的原则

这测试成套工具申请胶质金子immunochromatography技术为MPIgG抗体的定性测试当前在清液或血浆样品。 MPIgG抗体在共轭垫可能与胶质金子结合被标记老鼠反人的IgG固定的正面样品形成免疫复合物,并且沿膜小条移动由色谱法。 某些复合体由在T线Ag捉住预涂层的再组合MP-形成“金子被标记的老鼠反人的IgG- MPIgG Ab- MP Ag”和开发颜色。 剩余的自由复合体由在C线涂上的山羊反老鼠IgG抗体捉住开发颜色。 并且为消极样品,没有MPIgG抗体,在T线在仅C线不可能形成免疫复合物或开发颜色和colorate。

主要成分

  • 测试卡片(在T线(P1-P30)在C线涂上再组合MP抗原,山羊反老鼠IgG抗体) : 40测试卡片盒

  • 样品稀释剂: 1个瓶(5机器语言)

  • 产品指示: 1

储存条件和有效性的期间

  • 能被存放24个月在一个干燥地方在4à ‚ °到30Ã¢ê € ž Æ ’

  • 使用测试卡片在对大气一次被打开的1个小时之内,湿气在60%以下,或者立刻使用它,如果湿气更高。

样品请求

  • 清液和血浆样品从静脉血收集由常规方法。 血浆样品: 增加100ul肝素解答(1%)到5到10ml血液; 或柠檬酸钠解答(3.8%)对血浆根据1:9的比例; 或乙二胺四乙酸解答(15%) 0.04ml对5ml血浆。

  • 清液和血浆样品可以被存放在4Ã¢ê € ž Æ ’ 如果test在5家或者商店天之内完成在-20 Ã¢ê € ž Æ ’ 并且不超过3次的freeze-thaw。

  • 测试结果为溶血样品是无效的。

TEST PROCEDURE

  • Test preparation: 10μL, 100μL micropipettes, and matched tips

  • Test process: Make sure that before the test the temperature of the kit and the sample should be the same with the room temperature. Place the test card on a horizontal dry work surface. Add 10μL serum or plasma sample into the sample well or 100μL of sample dilution immediately. Observe the result in 15 to 20 minutes after the serum or plasma samples are added. The observation is invalid after 20 minutes.

TEST RESULTS EXPLAINED

The color developed on C line only: negative; color developed on both C line and T line: positive; color developed on T line only: invalid; color not developed on both C line and T line: invalid.

Note: Re-detection if the detected result is invalid. The invalid test cards should be dealt with as infectious pollutants and the temperature of the kit and sample should be the same with room temperature before pre-detection.

LIMITATION

  1. It was vulnerable to the visual error or the subjective judgment factors duplicate the detection when the stripe color is not obvious.

  2. The detection card is one of the assistant diagnostic methods; its test results are only for the reference and should not be the sole base for clinical diagnosis and its treatment. The positive results should be further verified by other methods also. Due to the limit of its detection sensitivity, the negative results should also be observed because the concentration of the antibodies is lower than the analysis sensitivity. It should combine with the clinical diagnosis, medical history, and other detection methods.

  3. The results will be unreliable for patients with impaired immune function or immunosuppressive treatment.

  4. Positive results will not only occur in the primary infection but also in the secondary infection.

  5. This test kit is a qualitative test and cannot be used for determining the antibody levels.

  6. It is used for the test of serum or plasma samples only, not for saliva, urine or any other body fluids testing.

PRODUCT PERFORMANCE INDICATORS

Positive coincidence rate: to the internal reference (+/+) =10/10; Negative coincidence rate (-/-) =10/10; precision (n=10): positive for all tests, and develop color equably; Minimum detection limit: positive end point is not less than 1:8 dilution of positive reference. The samples which is positive with toxoplasma IgM antibody (S/C value: âꀰ¤ 13.65), rubella virus IgM antibody (S/C value: âꀰ¤ 11.42), cytomegalovirus IgM antibody (S/C value: âꀰ¤ 13.41), herpes simplex virus II IgM antibody (S/C value: âꀰ¤ 12.53), Toxoplasma IgG antibody (S/C value: âꀰ¤ 13.45), rubella virus IgG antibody (S/C value: âꀰ¤ 10.39), cytomegalovirus IgG antibody (S/C value: âꀰ¤ 13.15), herpes simplex virus II IgG antibody (S/C value: âꀰ¤ 14.28), hepatitis B virus surface antigen (S/C value: âꀰ¤ 13.57), hepatitis C virus surface antigen positive (S/C value: âꀰ¤ 14.75), Treponema pallidum antibody (S/C value: âꀰ¤ 12.35), HIV (S/C values: âꀰ¤ 11.37), HEV-IgM (S/C values: âꀰ¤ 12.15), MP-IgM (S/C values: âꀰ¤ 9.23), MP-IgG (S/C values: âꀰ¤ 9.66), RSV-IgM (S/C values: âꀰ¤ 5.56) rheumatoid factor (âꀰ¤ 54IU/ml), antinuclear antibody (âꀰ¤ 1:640), staphylococcus aureus etc cannot affect results. There is an impact in the test when the lipid content of the sample is higher than 6mmol / L and the bilirubin level is higher than 40μmol / L.

PRECAUTIONS

  • When the kit test result is positive use other methods also for confirmation

  • Avoid the test card being exposed in the air for a long time since it can absorb moisture that can affect the test results. Use the test card within 1 hour once opened to the atmosphere and humidity is below 60%, or use it immediately if the humidity is higher.

  • The degree of coloration on the test line does not connect to the antibody titers in the test sample.

  • The color of C line is likely to abate when the content of the MP-IgG is extremely high in the sample. It is a normal phenomenon.

  • Be attentive to the potential biological risks. Wear necessary protective equipment, and deal with the waste as infectious material.




Trade Information
  • FOB Port
  • any port in China
  • Payment Terms
  • Others, Paypal, Western Union, Telegraphic Transfer (T/T), Letter of Credit at Sight (Sight L/C)
  • Supply Ability
  • 1,000,000 Per Month
  • Delivery Time
  • 15 Days
  • Sample Available
  • Yes
  • Sample Policy
  • Free samples available with shipping and taxes paid by the buyer
  • Packaging Details
  • cartons
  • Main Export Market(s)
  • Africa, Middle East, Western Europe, Eastern Europe, South America, North America, Central America, Australia, Asia
  • Main Domestic Market
  • All India
  • Certifications
  • GMP, ISO9001:2008, SFDA and ISO13485 Certificates.

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