Product Information
Contents: Biotin anti-mouse CD34
Catalog Number: 13-0341
Sizes: 50 ug, 100 ug, 500 ug
Formulation: Phosphate buffer pH 7.2, 150 mM NaCl, 0.09% NaN3
Storage Conditions: Store at 4°C. DO NOT FREEZE.
Clone: RAM34
Isotype: Rat IgG2a, κ
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Two-color surface staining of mouse bone marrow with anti-mouse CD34 (RAM34), FITC (left) and APC (right), and anti-mouse Hematopoietic Lineage Flow Panel Biotin followed by SA-PE. Total viable cells were used for analysis.
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Questions? Please consult our answers to frequently asked questions at
http://www.ebioscience.com/faq.
Description
The RAM34 monoclonal antibody reacts with mouse CD34, also known as mucosialin. It has been reported that the RAM34 antibody can be used to detect CD34
+Sca-1
+c-Kit
+ cells. Upon further optimization, we have determined that the most effective RAM34 formats for this combination of antigen detection are biotin, FITC, and Alexa Fluor 647. Preliminary data suggest that some antibody conjugates (such as PE and APC fluorochromes) may negatively impact detection of CD34. Interestingly, the PE RAM34 conjugate is suitable for the staining of epithelial cells (NIH3T3).
CD34, a highly glycosylated (approximately 90-120 kDa) member of the sialomucin family, is expressed by capillary endothelial cells, BM stoma and a small subpopulation of mouse bone marrow cells. RAM34 has been used to purify mouse HSCs to near homogeneity. Unlike in humans, primitive adult mouse bone marrow HSCs were detected in the CD34 low to negative fraction.
CD34 expressed on endothelial cells is a ligand for CD62L and plays a role in adhesion. Simultaneous staining of mouse bone marrow cells with a cocktail of antibodies to lineage markers (CD3, CD11b, Ly6G, TER-119 and
CD45R/B220) reveals a subset of total BM cells staining with RAM34 that can express undetectable to low levels of the mentioned lineage markers.
Applications Reported
For research use only, not for diagnostic or therapeutic use. This RAM34 antibody has been reported for use in flow cytometric analysis.
Applications Tested
The RAM34 antibody is routinely tested by flow cytometric analysis of a mouse cell line (NIH/3T3) and mouse bone marrow (BM) cell suspensions. When using conjugates of RAM34 for staining of mouse BM cells, we routinely perform a two-color analysis using RAM34 in combination with Lineage Cocktail (cat.
88-7774) to identify lineage-committed BM cells and better visualize the minor subset of Lineage negative/low cells that normally stain with RAM34 as reported in the literature. Gating strategies that exclude cells with low level expression of lineage markers may significantly decrease the total number of RAM34-positive cells. If using a Lineage Cocktail and/or other markers such as CD117/c-Kit or Ly6AE/Sca-1, it is best to analyze data on two-color plots (dot-plots or contour-plots, etc.) for best visualization of the staining. If you are using only one-color staining, analyze data as a two-parameter plot of RAM34 staining vs. Forward Light Scatter (FSC). Collecting and analyzing >10,000 total events per sample is helpful in increasing the number of RAM34-positive cells.
It is recommended to use 1 µg per million BM cells in a 100 µl total staining volume. It is recommended that the antibody be carefully titrated for optimal performance in the assay of interest. For more detailed information on staining with RAM34, please reference the following publication
PubMed.
References
Osawa M, Hanada K, Hamada H, Nakauchi H. 1996. Long-term lymphohematopoietic reconstitution by a single CD34-low/negative hematopoietic stem cell. Science. 273(5272):242-5.
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