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Secondary

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Product group Antibodies
OriGene
ApplicationsFlow Cytometry, ImmunoFluorescence
ReactivityRat
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Product group Antibodies
OriGene
ApplicationsFlow Cytometry, ImmunoFluorescence
ReactivityRat
  • SizePrice
Product group Antibodies
OriGene
ApplicationsELISA
ReactivityRat
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Product group Antibodies
OriGene
ApplicationsFlow Cytometry, ImmunoFluorescence, ELISA
ReactivityRat
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<strong>Immunofluorescent Staining:</strong> BALB/c splenocytes were incubated with Rat IgM Isotype Control, Rat anti-Mouse CD22 (2D6, Rat IgG1), Rat anti-Mouse CD8 (53-6.7, Rat IgG2a), Rat anti-Mouse CD45 (LCA) (I3/2.3, Rat IgG2b), Rat anti-Mouse CD3(C363.29B, Rat IgG2c), and Rat anti-Mouse CD45RC (GL24, rat IgM). After washing, the cells were stained with PE-labeled Mouse Anti-Rat IgM. Small Lymphocytes were gated and analyzed on a FACScan(TM) flow cytometer (BDIS, San Jose, CA). Amount Used: &lt; / = 0.02 µg/10e6 cells.
Product group Antibodies
OriGene
ApplicationsFlow Cytometry, ImmunoFluorescence
ReactivityRat
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Product group Antibodies
OriGene
ApplicationsFunctional Assay
ReactivityRat
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<strong>B Cell Stimulation:</strong> 5 x 10e5 SD Rat splenocytes were incubated with the indicated concentrations of purified Mouse F(ab')2 Anti-Rat IgM, clone M2A1, for 48 hours. B cell proliferation was determined by 3H-thymidine
incorporation assay. Amount Used: &lt; / = 10 μg/mL
Product group Antibodies
OriGene
ApplicationsFunctional Assay
ReactivityRat
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Product group Antibodies
OriGene
ApplicationsELISA
ReactivityRat
  • SizePrice
Product group Antibodies
OriGene
ApplicationsFlow Cytometry, ELISA
ReactivityRat
  • SizePrice
Product group Antibodies
OriGene
ApplicationsFlow Cytometry
ReactivityRat
  • SizePrice
Product group Antibodies
OriGene
ApplicationsELISA
ReactivityRat
  • SizePrice
Product group Antibodies
OriGene
ApplicationsFlow Cytometry, ELISA
ReactivityRat
  • SizePrice

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