anti-CD33 antibody product blog
Tags: Antibody; Monoclonal Antibody; CD33; anti-CD33 antibody;
The CD33 n/a (Catalog #MBS8504163) is an Antibody produced from Mouse and is intended for research purposes only. The product is available for immediate purchase. The Mouse anti-Human CD33, Purified mAb reacts with Human and may cross-react with other species as described in the data sheet. MyBioSource\'s CD33 can be used in a range of immunoassay formats including, but not limited to, Flow Cytometry (FC/FACS), Immunofluorescence (IF). Researchers should empirically determine the suitability of the CD33 n/a for an application not listed in the data sheet. Researchers commonly develop new applications and it is an integral, important part of the investigative research process.To buy or view more detailed product information and pricing, please click on the technical datasheet page below:
Please refer to the product datasheet for known applications of a given antibody. We\'ve tested the Mouse anti-Human CD33, Purified mAb with the following immunoassay(s):
Testing Data
4A6C5 reacts with CD33 andtigen, a 67 kDa type I transmembrane glycoprotein present on myeloid progenitors, monocytes andgranulocytes. CD33 is absent on lymphocytes, platelets, erythrocytes, hematopoietic stem cells and non-hematopoietic cystem. CD33 antigen can function as a sialic acid-dependent cell adhesion molecule and involved in negative selection of human self-regenerating hemetopoietic stem cells. This clone is cross reactive with non-human primate * identification of acute myelogenousnleukemia. Negative selection for human self-regenerating hematopoietic stem cells.
Experimental Methods: 1.Take 100mul peripheral blood anticoagulated by EDTA and add to the bottom of 5ml tube;
2.Add appropriate amount of antibody to the bottom of flow tube mixing with the whole blood, incubate for 30 minutes at room temperature;
3.Add 2 ml1�RBC lysis buffer, incubate for 10 minutes after mixing, dissolve red blood cells (recommended: RBC lysing Solution 10�);
4.Sample tube is set to 1000 rpm centrifugation for 5 minutes, discard the supernatant;
5.Add 2 ml PBS wash buffer to resuspend the cells, then 1000 rpm centrifugation for 5 minutes, discard the supernatant;
6.Add appropriate amount of fluorescent-labeled anti-mouse IgGs and incubate for 20 minutes away from light at room temperature.
7.Repeat step 5.
8.Add 0.5 ml PBS wash buffer to resuspend the cells and detect by flow cytometry (sample should be determined on the day on the machine and can also be added fixation overnight at 4 degree C then measured).
[PBS wash buffer: PBS +1% FBS +0.1% NaN3]
[Cell fixation: 2% formaldehyde solution]. In general, we may offer more than one antibody to a given target to enable options for the researcher. Available antibodies recognizing CD33 are readily searchable from our website. Different antibodies against the same target such as CD33 may be optimized or tested for different applications and species. This enables researchers to select the option that may be best for their model system, to screen more than antibody to determine which one may be best for their model system, as well as to use more than one antibody to follow up on and validate their results.