Human GloLIVE TRA-1-60(R) NorthernLights™ NL557-conjugated Antibody
Human GloLIVE TRA-1-60(R) NorthernLights™ NL557-conjugated Antibody Summary
To detect TRA-1-60(R) expression in live cells by immunocytochemical staining.
Why confirm marker expression in live cells before colony selection?
Maintaining pluripotent human embryonic stem cells and deriving induced pluripotent stem cells require colony selection and cell expansion. Picking colonies that contain pluripotent stem cells is typically achieved by manually analyzing colony morphology. Unfortunately, this critical process is time-consuming and labor-intensive.
In addition, morphology-based colony selection does not consistently guarantee pluripotent starting populations, since cells can fail to be fully reprogrammed or can naturally differentiate within a colony.
To address this need, R&D Systems offers GloLIVE™ antibodies that allow researchers to confirm stem cell marker expression in live cells before colony selection.
Live pluripotent stem cell imaging:
- Promotes the selection of high quality, undifferentiated stem cell colonies to reduce experimental variation.
- Verifies stem cell pluripotency in 30 minutes, ensuring efficient use of time and reagents.
- Allows for the continued culture of pluripotent cells with no adverse effects on cell proliferation or stemness following staining.
- GloLIVE NL557-conjugated Mouse Anti-Human TRA-1-60(R) Monoclonal Antibody.
- Supplied as 50X concentration of antibody in 0.5 mL PBS
Azide free and endotoxin tested (= 5 EU/mL), this antibody can be used for 12 tests, if a staining volume of 2 mL is used.
This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are guaranteed for 1 year from date of receipt.
Detection of TRA-1-60(R) in Live BG01V Human Embryonic Stem Cells. The stem cell marker TRA-1-60(R) was visualized in live BG01V human embryonic stem cells using a GloLIVE NL557-conjugated Mouse Anti-Human TRA-1-60(R) Monoclonal Antibody (Catalog # NLLC4770R; red). The nuclei were counterstained with Hoechst 33342 (blue). Positive staining for TRA-1-60(R) in human stem cells is an indicator of pluripotency.
TRA-1-60 is a monoclonal antibody raised against a cell surface antigen of human embryonal carcinoma (EC) cells (1). The TRA-1-60 epitope is also found on human embryonic stem (ES) cells and primordial germ cells, and TRA-1-60 serves as a serum marker in patients with germ cell tumors (2‑4). Investigation into the identity of the TRA-1-60 epitope demonstrated that it is a carbohydrate carried by a cell surface, sialylated, keratan sulfate proteoglycan (5). Subsequent evidence implicated podocalyxin as a carrier for the TRA-1-60 epitope (6).
- Andrews, P. et al. (1984) Hybridoma 3:347.
- Thomson, J. et al. (1998) Science 282:1145.
- Giwercman, A. et al. (1993) Cancer 72:1308.
- Marrink, J. et al. (1991) Int. J. Cancer 49:368.
- Badcock, G. et al. (1999) Cancer Res. 59:4715.
- Schopperle, W. and W. DeWolf (2007) Stem Cells 25:723.
Refer to the product datasheet for complete product details.
Use aseptic technique and sterile culturing conditions to prevent contamination.
GloLIVE NL557-conjugated Mouse Anti-Human TRA-1-60(R) Monoclonal Antibody. (Catalog # NLLC4770R):
Other Supplies Required
- Stem cell culture media
- Human or mouse pluripotent stem cells
- Pipettes and pipette tips
- Serological pipette
- 37 °C and 5% CO2 incubator
- Fluorescence microscope
Live Cell Immunocytochemistry Procedure Overview
To ensure sterility of cultures, all steps should be performed under sterile conditions.
- Add fluorochrome-conjugated primary antibody in appropriate culture media to cells.
- Incubate for 30 minutes.
- Replace with fresh culture media.
- Visualize using a fluorescence microscope.
Note: Culture with GloLIVE antibodies does not appear to affect cell proliferation or stemness as assayed by proliferation curves for 3 days post-antibody incubation and expression levels of TRA-1-60(R) and Oct-3/4.
Citations for Human GloLIVE TRA-1-60(R) NorthernLights™ NL557-conjugated Antibody
R&D Systems personnel manually curate a database that contains references using R&D Systems products. The data collected includes not only links to publications in PubMed, but also provides information about sample types, species, and experimental conditions.
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Robust and highly efficient hiPSC generation from patient non-mobilized peripheral blood-derived CD34+ cells using the auto-erasable Sendai virus vector
Authors: T Okumura, Y Horie, CY Lai, HT Lin, H Shoda, B Natsumoto, K Fujio, E Kumaki, T Okano, S Ono, K Tanita, T Morio, H Kanegane, H Hasegawa, F Mizoguchi, K Kawahata, H Kohsaka, H Moritake, H Nunoi, H Waki, SI Tamaru, T Sasako, T Yamauchi, T Kadowaki, H Tanaka, S Kitanaka, K Nishimura, M Ohtaka, M Nakanishi, M Otsu
Stem Cell Res Ther, 2019;10(1):185. 2019
Amenable epigenetic traits of dental pulp stem cells underlie high capability of xeno-free episomal reprogramming
Authors: S Thekkepara, S Sriram, S Subramania, S Cheng, WK Ong, S Rozen, NHA Kasim, S Sugii
Stem Cell Res Ther, 2018;9(1):68. 2018
What is the recommended starting confluence to observe staining?
The optimal confluence would depend on the purpose of the staining. If the plan is to use all the cells in the flask after they have proliferated, then one can wait for the cells to become confluent or almost confluent (80-90% confluent) and then check the staining. If the goal is to to check on the cells mid-way through their growth and there are sufficient cells in the flask, one could check the staining then as well. The staining is not dependent on how many cells are in the flask, as long as there are sufficient cells.
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