PE Anti-SAM Monoclonal Antibody Clone 84-3 | MAF00202-50

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50 µl
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PE Anti-SAM Monoclonal Antibody Clone 84-3 | MAF00202-50 | Arthus Biosystems

Product name         

R-Phycoerythrin-anti-SAM 1

Catalog Number     



R-Phycoerythrin (R-PE) conjugated anti-S-adenosylmethionine monoclonal antibody clone 84-3


MAF00202 shows the same specificity as un-conjugated mouse anti-SAM monoclonal antibody MA00202.




Storage instructions          

Store at 2-8°C in dark, do not freeze.


2-4nrig/m1 or lot specific

Storage buffer                    

50mM Tris, 150mM NaCI, pH8.0, 0.2% BSA (Sigma), 0.09%NaN3

Dilution buffer                   

PBS, pH 7.4, 1% fetal bovine serum or 0.5% BSA, 0.09%NaN3


>95% purified with Sephadex G-25 and Sephacryl S-300, free from un-conjugated antibody and R-Phycoerythrin



Clone number                    


Immunoglobin isotype      

mouse IgG2b

Research Areas                  

  • Methylation of biomolecules (DNA, RNA, proteins, hormones, neurotransmitters, etc.)
  • One-carbon metabolism
  • Signal Transduction
  • Metabolism
  • Pathways and Processes Cancer
  • Arthritis
  • Neurodegenerative diseases
  • Atherosclerosis
  • Liver diseases
  • Kidney diseases


The use of MAF00202 in the following applications has been tested. The application notes include recommended and tested dilutions. Optimal dilutions/concentrations should be determined by the end user based on the test environment and purposes.


  1. Flow Cytometry (FCM): 30-90 lag/ml
  2. lmmunofluorescence Laser Scanning Confocal Microscopy (LSCM): 30-60 lag/ml

Figure 1: Immunofluorescence (IF) LSCM results of normal liver cells L02 cultured in RPMI 1640 with 10%  for 40h (A1-A4) double stained with AF488-anti-SAH 839-6 (Cat# MAF00302) at 40pg/m1 and R-PE-anti-SAM  84-3 (Cat# MAF00202) at 40pg/m1 followed by DAPI staining. Hepatocellular carcinoma cell line HepG2 cells were cultured for 40h (B1-B4) and double stained with AF488-anti-SAH 839-6 (Cat# MAF00302) at 60pg/m1 and R-PE-anti-SAM 84-3 (Cat# MAF00202) at 60pg/m1 followed by DAPI staining. Photography was performed under the laser scanning confocal microscope Zeiss LSM 780 (x630). Different views are as follows: DAPI  (A1, B1); AF488 for SAH (A2, B2); R-PE for SAM (A3, B3); Overlap of all the three fluorescent signals (A4, B4). Expression patterns of SAM and SAH are different between L02 and HepG2 cells. In this case, both SAM and SAH are seen more in cytoplasm (more in mitochondria areas) than nuclear.

Figure 2 Flow Cytometry of L02 (B) and HepG2 (C) cells double stained with Alexa Fluro 488 conjugated anti-SAH antibody 839-6 (Cat# MAF00302) at 45 pg/ml and R-PE conjugated anti-SAM antibody 84-3 (Cat# MAF00202) at 45 pg/ml. 100% confluent cells (cultured in RPMI 1640 with 10% for 40h) were fixed and permeabilized with the nuclear fixation/permeabilization buffer (eBioscience 00-5523 FoxP3_TF Staining Buffer Set) and then double stained with antibodies indicated above. Cells were used for analysis with BD FACSCanto II Flow Cytometer. Both SAM and SAH are expressed ubiquitously yet rather dynamically. A: blank.

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