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Rapid 人 NGAL XpressCard

LFCIA, rapid 适用: 人 Plasma, Urine
产品编号 ABIN2860639
发货至: 中国
  • 抗原 See all Lipocalin 2 (LCN2) 试剂盒
    Lipocalin 2 (LCN2)
    适用
    • 7
    • 5
    • 3
    • 3
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    检测范围
    50-1000 ng/mL
    最低检测浓度
    50 ng/mL
    应用范围
    Lateral Flow Chromatographic Immunoassay (LFCIA), Rapid Test (rapid)
    原理
    The test is for qualitative detection of NGAL in human urine, but dose not indicate the quantity of NGAL.
    样品类型
    Plasma, Urine
    灵敏度
    50 ng/mL
    产品特性
    Neutrophil Gelatinase-Associated Lipocalin (NGAL) XpressCard utilizes the principle of Immunochromatography (also called as lateral flow immunoassay, LFIA).
    A mouse anti- human NGAL antibody is immobilized on the nitrocellulose membrane as the test line (T line) in the test window of the test device.
    As the test sample flows through the membrane assembly within the test device, NGAL within the sample is bound by a sencond mouse anti-human NGAL antibody conjugated with colloidal gold and released from the sample pad.
    This antigen-antibody complex moves further on the membrane to the test region where it is immobilized by the first anti-human NGAL coated on the membrane, leading to the formation of a colored band, which confirms a positive test results.
    Absence of this colored band in the test window indicates a negative test result.
    A built-in control line (C line) will always appear in the test window, regardless of the presence or absence of NGAL in the Specimen.
    组件
    2 cassetts per pouch
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  • 样本量
    100 µL
    实验时间
    5 min
    样品收集
    1. No prior special preparation of the patient is required before sample collection by approved techniques.
    2. Fresh morning urine is preferable. Urine may be stored at 2-8 °C up to 3 days in case of delay in testing. For long-term storage, freeze the specimen at -20 °C for 3 months or -70 °C for longer periods.
    3. Repeated freezing and thawing of the specimen should be avoided.
    4. Do not use haemolysed, clotted, contaminated, lipamic and viscous/turbid specimen.
    5. Specimen containing precipitates or particulate matter must be centrifuged and the clear supernatant only used for testing.Do not heat inactivate the Sample.
    实验流程

    1) Place the card Horizontally.
    2) Add 100 μL of biological fluids directly to the Sample Well.
    3) Wait for 3-5 Minutes.

    结果分析

    Results:

    Negative:
    Only the control C line appears.

    Positive:
    Both the C line and test T line appear, which indicates the presence of NGAL.

    Invalid: If after 20 minutes no C line appears, the result is invalid. The test should be repeated with a new Device.

    限制
    仅限研究用
  • 注意事项
    1. This kit is for IN VITRO research use and should be handled by PROFESSIONALS.
    2. Read the instructions carefully before performing the test.
    3. Follow standard lab procedure and biosafety guidelines, and handle all human specimens as potentially infectious. Wear gloves during the whole procedure.
    4. When the assay procedure is complete, dispose specimens after autoclaving them at 121°C for at least 20 min. Alternatively, they can be treated with 0.5% Sodium Hypochlorite for 1-2 hours before Disposal.
    储存条件
    RT
    储存方法
    Store the cards in their original packaging at room temperature.
    This product is stable for up to 18 months from the certified date.
    Freezing the strips is not Recommended.
    有效期
    18 months
  • 抗原
    Lipocalin 2 (LCN2)
    别名
    NGAL (LCN2 产品)
    别名
    LCN2 Kit, 24p3 Kit, MSFI Kit, NGAL Kit, AW212229 Kit, Sip24 Kit, lipocalin 2 Kit, LCN2 Kit, Lcn2 Kit
    背景
    NGAL, also known as oncogene 24p3 or Lipocalin-2 (LCN2) is involved in innate immunity by sequestrating iron that in turn limits bacterial growth.
    It is expressed in neutrophils and in low levels in the kidney, prostate, and epithelia of the respiratory and alimentary tracts.
    In the case of acute kidney injury (AKI), NGAL is secreted in high levels into the blood and urine within 2 hours of injury.
    Because NGAL is protease resistant and small, the protein is easily excreted and detected in the urine.
    NGAL levels in patients with AKI have been associated with the severity of their prognosis and can be used as a biomarker for AKI. NGAL can also be used as an early diagnosis for procedures such as chronic kidney disease, contrast induced nephropathy, and kidney transplant.
    Kidney health is most frequently measured by serum creatinine.
    Serum creatinine is a marker of kidney function, whereas NGAL is a marker of kidney injury. NGAL levels are a more precise and sensitive marker for diagnosing AKI than serum creatinine levels.
    In fact, the increase in urinary excretion of NGAL has been proven to be due to tubular alterations that take place before any damage can be detected by other methods.
    Therefore, monitoring NGAL levels reduces delayed AKI diagnosis and treatment. Using a more sensitive and specific marker allows for earlier diagnosis, correct responses to AKI, and reduced risk of morbidity and Mortality.
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