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FITC Mouse Anti-Rat Ig, κ Light Chain Antibody (S-4515)

价格 344.00 供应商现货 : 3-5个工作日
货号 S0B80113
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产品规格
  • 宿主来源

    Mouse
  • 抗原名称

    Rat Ig, κ Light Chain
  • 克隆号

    S-4515
  • 抗体类型

    Mouse mAb
  • 抗体同种型

    IgG1
  • 反应种属 ?

    Rt
  • 阳性样本

    C57BL/6 mouse splenocytes
  • 纯化方式

    Protein G
  • 浓度

    0.5 mg/ml
  • 标记

    FITC
  • 性状

    Liquid
  • 缓冲体系

    PBS, 1% BSA, 0.3% Proclin 300

  • 储存条件

    12 months from date of receipt / reconstitution, 2 to 8 °C as supplied

  • 应用

    FCM

  • 稀释度

    应用 稀释度 推荐种属
    FCM 0.25μg per million cells in 100μl volume Rt
背景介绍
  • Ig κ Light Chain is one of the two types of light chains (the other being the λ light chain) that constitute antibody (immunoglobulin) molecules. Composed of approximately 220 amino acids, it is linked to the heavy chain via disulfide bonds, together forming the basic structure of antibodies. In humans, the κ light chain is encoded by the IGK gene family located on chromosome 2, and its production involves the rearrangement of V (variable), J (joining), and C (constant) gene segments to generate high diversity for recognizing countless antigens. Under physiological conditions, the ratio of κ to λ light chains in serum is approximately 2:1, but this ratio may change under certain pathological conditions. For example, in multiple myeloma, abnormal plasma cells may overproduce free κ light chains (i.e., Bence Jones proteins), which can be excreted in the urine. Therefore, measuring κ light chains and their ratio to λ light chains in blood or urine holds important clinical value for diagnosing and monitoring B-cell-related disorders such as myeloma, amyloidosis, and lymphoproliferative diseases.

  • 流式分析

    • Flow cytometric analysis of rat Ig, κ light chain expression on C57BL/6 mouse splenocytes. C57BL/6 mouse splenocytes were stained with Alexa Fluor® 700 Rat Anti- Mouse IgD Antibody and either FITC Mouse IgG1 Isotype Control (left panel) or FITC Mouse Anti-Rat Ig, κ Light Chain Antibody (right panel) at 0.5 μl/test. Flow cytometry and data analysis were performed using Agilent NovoCyte Quanteon and FlowJo™ software.

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