Immunohistochemistry Collagen Type VII Rabbit

Get tips on using CD34 Antibody (MEC 14.7): sc-18917 to perform Immunohistochemistry Mouse - CD34

Get tips on using IRE1α Antibody (B-12): sc-390960 to perform Immunohistochemistry Mouse - IRE1α

Get tips on using PR Antibody (F-4): sc-166169 to perform Immunohistochemistry Mouse - PR

Get tips on using PR Antibody (AB-52): sc-810 to perform Immunohistochemistry Mouse - PR

Get tips on using VWF Antibody (C-12): sc-365712 to perform Immunohistochemistry Mouse - vWF

Get tips on using VEGF Antibody (C-1): sc-7269 to perform Immunohistochemistry Mouse - VEGFA

Get tips on using Anti-Peptide YY/PYY antibody (ab131246) to perform Immunohistochemistry Mouse - PYY

Get tips on using Phospho-Histone H3 (Ser10) Antibody #9701 to perform Immunohistochemistry Mouse - PHH3

Cell cytotoxicity assays measure the ability of certain compounds or chemical mediators to reduce the viability of the cells. The term cell cytotoxicity assay can sometimes be used interchangeably with cell proliferation assay. Healthy living cells can be identified by the use of formazan dyes, protease biomarkers or by measuring ATP content. The formazan dyes are chromogenic products formed by the reduction of tetrazolium salts by dehydrogenases, such as lactate dehydrogenase (LDH) and reductases that are released during cell death. Common tetrazolium salts include INT, MTT, MTS and XTT. Cell cytotoxicity can also be measured by using the SRB and WST-1 assays. These assays can usually be used in a high-throughput fashion and can be quantitated by measuring absorbance, colorimetry or luminescence. All these assays require similar numbers of cell plating at the initiation, a time course of treatment with the cytotoxic agent and at least triplicates for each condition at every point of analysis. Cell shrinkage, plasma membrane blebbing, cell detachment, externalization of phosphatidylserine, nuclear condensation and ultimately DNA fragmentation are well-described features of apoptosis. The assays that rely on cell membrane integrity for their function, may not be able to quantify early apoptosis. Therefore, in order to distinguish early apoptotic vs. late apoptotic or necrotic cells, additional flow cytometry techniques can be used. A combination of Annexin V and PI (propidium iodide) can be used to distinguish early (Annexin V+/PI-) and late apoptotic (Annexin V+/PI+) cells. Sometimes, caspase assays are used in order to differentiate the stages of apoptosis.

Acid phosphatase detection heavily relies on determining the concentration of tartrate-resistant acid phosphatase (TRAP) in the sample. Hence, sample preparation is very crucial and it should be done strictly as per kit manufacturer instructions to avoid any inconsistency and poor sensitivity.