The bottom image of Fig. 2b indicates the microscopic image of ex vivo mouse tissue based on the raster scanning [10].
A sensitive and selective method was elaborated for the determination of the anticonvulsant compounds levels in mice brain tissue, based on HPLC with diode array detector (DAD).
When tissue-specific differentially methylated regions (T-DMRs) in human and mouse tissues including heart, colon, kidney, testis, spleen, and muscle were compared, they could be distinguished clearly according to the corresponding tissues based on their methylation status [ 27].
To address these limitations, tissue based color targets have been proposed such as a section of mouse embryo stained in a standard way.
Total RNA was extracted from BAT, carefully excised to get rid of surrounding tissue based on the texture and color, of 6 WT and 6 Taf7l KO mice.
In this study, we compared one corresponding tissue based method and three co-expression based methods for assessing conservation of gene expression, in terms of their pair-wise agreements, using a frequently used human-mouse tissue expression dataset.
To compare the mouse oocyte proteome with other mouse tissue proteomes, we generated a combined database for the mouse based on the following mouse tissues and cell cultures characterized by LC-MS/MS: mouse heart [ 51], liver [ 51- 53], brain [ 51, 54], lung [ 51, 55], kidney [ 51], spleen [ 56], placenta[ 51], cortical neurons cell culture[ 57], sperm [ 58], islet alpha-cell culture [ 59].
Based on Northern analysis of mouse tissues, a 2.4 kilobase transcript is present in many tissues.
Properties of mouse gene expression were defined based on the microarray data of 61 mouse tissues (Su et al. 2004).
