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- 详细信息
- 文献和实验
- 技术资料
- 英文名:
Ham's F-12K (Kaighn's) Medium
- 规格:
500ml
描述
Ham's F-12K (Kaighn's) Medium is a modification of Ham's F-12 Nutrient Mixture. Ham's F-12K (Kaighn's) Medium was developed for primary human hepatocytes, as well as for some rat and chicken liver cells in a reduced serum environment.This F-12K (Kaighn's) Medium is manufactured as follows:
| With | Without |
| • L-glutamine | • HEPES |
| • Phenol Red |
The complete formulation is available.
Using Ham's F-12K
Ham's F-12K (Kaighn's) Medium contains many components not found in traditional basal media, such as putrescine, thymidine, hypoxanthine, zinc, and higher levels of all amino acids and sodium pyruvate. These additions allow the medium to be supplemented with very low levels of serum or defined components, for some cell types. Ham's F-12K (Kaighn's) Medium contains no proteins or growth factors, and is therefore often supplemented with growth factors and Fetal Bovine Serum (FBS). The FBS concentration must be optimized for each cell line. Ham's F-12K (Kaighn's) Medium uses a sodium bicarbonate buffer system (2.5 g/L), and therefore requires a 5–10% CO2 environment to maintain physiological pH.
Dual-site cGMP manufacturing
For supply chain continuity, we manufacture Ham's F-12K (Kaighn's) Medium at two separate facilities, located in Grand Island, NY and Scotland, UK. Both sites are compliant with cGMP-manufacturing requirements, are certified to ISO 13485, and are registered with the FDA as medical device manufacturers.
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文献和实验x-S的质控图是检验主管技师考试要求掌握的内容,医学教育网搜集整理相关内容供大家参考。 后来Henry和Segalove对X-R质控图进行了修改,他们以20次质控物的单次测定结果,计算其x及标准差(s),以x±2S为警告限,以x±3S为失控限,这也就是现在广为应用的Levey—Jennings质控图,从质控图的体系来说,它属于单值质控图中的x-S质控图。这个质控图适用于质控数据取得需要较长周期或费用昂贵时,其方法比较简单,易于推广。实际上这两种质控图的检定力是不同的,原
Henry和Segalove对X-R质控图进行了修改,他们以20次质控物的单次测定结果,计算其x及标准差(s),以x±2S为警告限,以x±3S为失控限,这也就是现在广为应用的Levey-Jennings质控图,从质控图的体系来说,它属于单值质控图中的x-S质控图。这个质控图适用于质控数据取得需要较长周期或费用昂贵时,其方法比较简单,易于推广。实际上这两种质控图的检定力是不同的,原Levey-Jennings质控图优于用单次测定结果绘制的医学`教育网搜集整理质控图,且提供了更多的质量
X-S图法由于它只需要单一浓度的未定值血清,绘图方法简单易懂,有较为成熟的理论和实际经验。因此,成为国内外目前采用最广泛的一种常规室内质量控制方法。一般步骤和具体做法如下: ⒈最佳条件和常规条件下的变异的测定及计算 选择含量均匀、稳定性良好的未定值质控血清,在“最佳条件”,对该批血清反复测定(至少20份),计算出20个结果的X、S和CV,此CV即为最佳条件下的变异(optimal condition variance,OCV)。取测过OCV的质量
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