ASTM F1906-1998(2003)
用酶标记免疫分析试验、淋巴细胞扩散和细胞移动评价生物配伍中免疫反应的标准操作规程

Standard Practice for Evaluation of Immune Responses In Biocompatibility Testing Using ELISA Tests, Lymphocyte, Proliferation, and Cell Migration


ASTM F1906-1998(2003) 中,可能用到以下仪器设备

 

Luminex 200 液相芯片仪

Luminex 200 液相芯片仪

默克生命科学

 

Guava easyCyte 12系统

Guava easyCyte 12系统

默克生命科学

 

Guava easyCyte 6系统

Guava easyCyte 6系统

默克生命科学

 

Guava easyCyte 6HT系统

Guava easyCyte 6HT系统

默克生命科学

 

guava easyCyte 5系统

guava easyCyte 5系统

默克生命科学

 

Guava easyCyte 5HT系统

Guava easyCyte 5HT系统

默克生命科学

 

默克Millicell ERS-2 电阻仪

默克Millicell ERS-2 电阻仪

默克生命科学

 

Vectra™全自动定量病理学工作站(6片连载型)

Vectra™全自动定量病理学工作站(6片连载型)

珀金埃尔默企业管理(上海)有限公司PerkinElmer

 

Vectra™全自动定量病理学工作站200片连载型

Vectra™全自动定量病理学工作站200片连载型

珀金埃尔默企业管理(上海)有限公司PerkinElmer

 

赛默飞Attune NxT声波聚焦流式细胞仪

赛默飞Attune NxT声波聚焦流式细胞仪

赛默飞 AppliedBiosystems

 

autoMACS Pro 全自动磁性细胞分选仪

autoMACS Pro 全自动磁性细胞分选仪

德国美天旎生物技术和贸易(上海)公司Miltenyi Biotec

 

MACSQuant® Tyto 流式细胞分选仪

MACSQuant® Tyto 流式细胞分选仪

德国美天旎生物技术和贸易(上海)公司Miltenyi Biotec

 

美天旎MACSQuant® X高通量流式细胞仪

美天旎MACSQuant® X高通量流式细胞仪

德国美天旎生物技术和贸易(上海)公司Miltenyi Biotec

 

MACSQuant® 流式细胞仪

MACSQuant® 流式细胞仪

德国美天旎生物技术和贸易(上海)公司Miltenyi Biotec

 

MACSQuant® VYB流式细胞仪

MACSQuant® VYB流式细胞仪

德国美天旎生物技术和贸易(上海)公司Miltenyi Biotec

 

ClonePix 2细胞克隆筛选系统

ClonePix 2细胞克隆筛选系统

美谷分子仪器(上海)有限公司

 

皮升泵LPP01-100(细胞注射器)-LongerPump

皮升泵LPP01-100(细胞注射器)-LongerPump

保定兰格恒流泵有限公司

 

 

 

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标准号
ASTM F1906-1998(2003)
发布日期
1998年
实施日期
废止日期
2011-03-01
中国标准分类号
C04
国际标准分类号
11.020
发布单位
US-ASTM
代替标准
No_Replacement
适用范围

1.1 This practice covers the introduction of a foreign substance into mammalian body that may induce the formation of an immune response. The immune response may lead to inadvertent tissue damage and be an undesirable event. In the standard protocols for biocompatibility testing, various studies in animals are done. These animals or their blood and tissues could be used to determine if immune responses have occurred and what types have occurred. At the current time, the immunologic testing in biocompatibility protocols is very limited. Techniques can be developed in the future which are simple, reliable, and sensitive.

1.2 It is the purpose of this practice to delineate some possible test methods. It must be remembered that these are protocols for use in biocompatibility testing, they are not diagnostic tests for evaluation of human conditions. Diagnostic test for use on humans must go through evaluation at the regulatory agencies. The tests described here are clearly adaptable for use in humans and can be used for research purposes and provide data in clinical trials, but are not necessarily cleared for diagnostic purposes. This practice presents selected methods. Other validated methods may be equally applicable.

1.3 The values state in SI units are to be regarded as the standard.

1.4 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety and health practices and determine the applicability of regulatory limitations prior to use.


ASTM F1906-1998(2003) 中可能用到的仪器设备





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