Immunohistochemistry chk2 Rabbit IgG Human

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Get tips on using SurePrint G3 Human CGH Microarray Kit, 4x180K to perform Microarray Comperative genomic hybridization - Human SKBR3

Products Agilent Technologies SurePrint G3 Human CGH Microarray Kit, 4x180K

Get tips on using GeneChip™ Human Genome U133A 2.0 Array to perform Microarray Comperative genomic hybridization - Human Tumor

Products Thermo Fisher Scientific GeneChip™ Human Genome U133A 2.0 Array

Get tips on using MammoCult™ Human Medium Kit to perform Stem cell culture media hMammospheres

Products STEMCELL technologies MammoCult™ Human Medium Kit

Get tips on using Human MesoEndo Cell Growth Medium to perform Mammalian cell culture media HCAEC

Products Cell Applications Inc Human MesoEndo Cell Growth Medium

Get tips on using Human MesoEndo Cell Growth Medium to perform Mammalian cell culture media HCtASMC

Products Cell Applications Inc Human MesoEndo Cell Growth Medium

Get tips on using Human MesoEndo Cell Growth Medium to perform Mammalian cell culture media HCtAEC

Products Cell Applications Inc Human MesoEndo Cell Growth Medium

Get tips on using Anti-p62 (SQSTM1) (Human) pAb to perform Autophagy assay cell type - A549

Products MBL international corporation Anti-p62 (SQSTM1) (Human) pAb

RNA siRNA / miRNA gene silencing Human Primary Endometrial Stromal Cells IGFBP1 (Insuline-like growth factor binding protein-1) Lipid

Flow cytometry is an immunophenotyping technique whereby sing cell suspensions are stained for either cell surface markers or intracellular proteins by fluorescently-labelled antibodies and analyzed with a flow cytometer, where fluorescently-labelled molecules are excited by the laser to emit light at varying wavelengths, which is then detected by the instrument. There are several key criteria which are required to be kept in mind while designing a flow experiment- 1. Antibody titration (optimal dilution of antibodies should be calculated in order to avoid over- or under- saturated signals for proper detection of surface and intracellular markers), 2. Precision (3 or more replicates of the sample should be used per experiment), 3. Specificity (proper isotype controls should be included in the experiment), 4. Day-to-day variability (experiments should be repeated 3 or more times to ensure consistency and avoid variability due to flow cytometer settings), 5. Antibody interaction (Fluorescence minus one or FMO should be used, which is the comparison of signals from panel minus one antibody vs. the full panel), and 6. Antibody stability (fluorescently-labelled antibodies should be stored at 4C).

Proteins Flow cytometry Anti-bodies Human CD49f/ITGA6

Get tips on using Anti-Human L1CAM Therapeutic Antibody Fab Fragment to perform Flow cytometry Anti-bodies Human - CD171/L1CAM

Products Creative BioLabs Anti-Human L1CAM Therapeutic Antibody Fab Fragment

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