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串联染料:在混合液中的稳定性及补偿考量

Tandem dyes: Stability in cocktails and compensation considerations.

作者信息

Johansson Ulrika, Macey Marion

机构信息

Haematology Oncology Diagnostics, Bristol Royal Infirmary, Bristol, BS2 8HW, United Kingdom.

出版信息

Cytometry B Clin Cytom. 2014 May;86(3):164-74. doi: 10.1002/cyto.b.21154. Epub 2014 Jan 10.

Abstract

BACKGROUND

The stability and performance of tandem-conjugated antibodies can be impaired when stored in antisera cocktails (Biancotto et al., J Immunol Methods 2011;363:245-261; Rawstron et al., Leukemia 2013;27:142-149). This, and the need for frequent re-compensation due to the possible spectral spillover variation between tandem lots, reduces the robustness of clinical flow cytometry panels that include tandems. Since tandems are required for standard 8-10 color screens, further studies of the stability of tandems in cocktails and their spillover variability are warranted.

METHODS

The performance of PE- and APC-tandems stored in cocktails was tested on fresh bone marrow, preserved blood and lyophilized cell samples over 1-, 6-, or 8-week periods, respectively, and their spillover matrices were compared. The observed correction factor differences were used as the basis for analyzing how the application of an incorrect compensation matrix could influence data interpretation.

RESULTS

Signal intensities and background fluorescence remained constant for all fluorochromes in the cocktails tested. Spillover correction factors for different PE-Cy7 mAbs did not exceed or were only marginally higher than those for non-tandem organic dye-conjugated mAb. By applying the correction factor differences observed between tandem mAb lots to clinical data, it was found that the over and under compensation would not alter the clinical interpretation.

CONCLUSIONS

Tandems can be safely stored and used in cocktails. However, each cocktail should be tested on relevant material prior to use. Exact compensation settings are a requirement for accurate data. Provided that careful evaluation of tandem compensation requirements is carried out, certain tandems may use a generic compensation matrix.

摘要

背景

串联共轭抗体在抗血清混合物中储存时,其稳定性和性能可能会受到损害(比安科托等人,《免疫学方法杂志》2011年;363:245 - 261;罗斯特龙等人,《白血病》2013年;27:142 - 149)。由于串联批次之间可能存在光谱溢出变化,需要频繁重新补偿,这降低了包含串联抗体的临床流式细胞术检测板的稳健性。由于标准的8 - 10色筛选需要串联抗体,因此有必要进一步研究串联抗体在混合物中的稳定性及其溢出变异性。

方法

分别在新鲜骨髓、保存血液和冻干细胞样本上,对储存在混合物中的PE和APC串联抗体进行1周、6周或8周的性能测试,并比较它们的溢出矩阵。观察到的校正因子差异被用作分析应用错误补偿矩阵如何影响数据解释的基础。

结果

在所测试的混合物中,所有荧光染料的信号强度和背景荧光保持恒定。不同PE - Cy7单克隆抗体的溢出校正因子不超过或仅略高于非串联有机染料偶联单克隆抗体的校正因子。通过将串联单克隆抗体批次之间观察到的校正因子差异应用于临床数据,发现过补偿和欠补偿不会改变临床解释。

结论

串联抗体可以安全地储存在混合物中并使用。然而,每种混合物在使用前都应在相关材料上进行测试。准确的数据需要精确的补偿设置。只要对串联补偿要求进行仔细评估,某些串联抗体可能使用通用补偿矩阵。

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