Immunohistochemical analysis of formaldehyde - fixed paraffin - embedded canine neuronal tissue sections, labelling GFAP with ab7260 at a dilution of 1/1000 incubated for 90 minutes at 25 °C.
Immunohistochemical analysis of human tonsil tissue labeling Ki - 67 with ab16667 at 1/200.
Immunohistochemical analysis of paraffin - embedded human prostate carcinoma using unpurified ab32518 at 1/50 dilution.
Immunohistochemical analysis of Formaldehyde fixed, frozen rat spleen tissue sections labelling CD3 with ab16669 at a dilution of 1/500.
Immunohistochemical analysis of Formaldehyde fixed, paraffin - embedded pig spleen tissue sections labelling CD3 with ab16669 at a dilution of 1/100.
Immunohistochemical analysis of Formaldehyde fixed, paraffin - embedded rat spleen tissue sections labelling CD3 with ab16669 at a dilution of 1/100.
Immunohistochemical analysis of human subcutaneous adipose tissue showed that both BMI and adipocyte size were strong predictors of the percentage of CD68 - expressing macrophages.
Immunohistochemical analysis of perigonadal, perirenal, mesenteric, and subcutaneous adipose tissue revealed that the percentage of cells expressing the macrophage marker F4 / 80 (F4 / 80 +) was significantly and positively correlated with both adipocyte size and body mass.
In all
our immunohistochemical analyses of PRLR in mouse mammary tissue, we used PRLR - deficient mammary glands as a negative control to test the specificity of the staining.
Not exact matches
Image
analysis of the
immunohistochemical studies displayed in A (staining with an anti-IAPP antibody) was performed to estimate the percentage
of islets containing amyloid deposits (E) and the load
of IAPP aggregates (F), calculated as the percentage
of the stained area compared with the total islet area.
C,
immunohistochemical analysis for KLF4 expression was conducted for primary breast tumors and brain metastatic tumors, and the numbers
of nuclear or cytosolic staining were assessed under microscope.
Using an antibody that recognizes the CD68 antigen we performed
immunohistochemical analysis on these human samples and calculated the percentage
of CD68 expressing cells (Figure 9).
Therefore, this work would assess the prognostic role
of the Cyclin D1 expression through
immunohistochemical stain by Cyclin D1 protein scoring and quantitative value by image
analysis (IOD).
To further confirm the alteration
of DDX3 expression in cancer specimens, the expression profiles
of DDX3 were examined in normal - tumor paired HCC samples by
immunohistochemical staining
analysis using specific anti-DDX3 antibody.
Because DDX3 harbors growth - suppressive ability and transcriptional modulation activity
of the p21waf1 / cip1 promoter, in this work we further examined the deregulated expression
of DDX3 in tumors by a cancer profiling array and
immunohistochemical staining
analysis.
Jacquemier J, Moles JP, Penault - Llorca F, Adelaide J, Torrente M, Viens P, Birnbaum D, Theillet C. p53
immunohistochemical analysis in breast cancer with four monoclonal antibodies: comparison
of staining and PCR - SSCP results.