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Jackson/AMCA IgG Fraction Monoclonal Mouse Anti-Fluorescein (FITC)/0.5 mg/200-152-037
  • Jackson/AMCA IgG Fraction Monoclonal Mouse Anti-Fluorescein (FITC)/0.5 mg/200-152-037

Jackson/AMCA IgG Fraction Monoclonal Mouse Anti-Fluorescein (FITC)/0.5 mg/200-152-037

價(jià)格: ¥1320.00 市場(chǎng)價(jià): 3520.00

貨號(hào): 200-152-037
品牌: Jackson
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    • Information IgG fraction Monoclonal Mouse Anti-Fluorescein may be used either as direct conjugates, or for more sensitivity, they can be used unconjugated followed by a conjugated anti-mouse IgG (H+L) for signal enhancement.Usage Physical State: Freeze-dried solid

      Storage and Rehydration: Store freeze-dried solid at 2-8°C. Rehydrate with the indicated volume of dH2O (see product specification sheet) and centrifuge if not clear. Prepare working dilution on day of use. Product is stable for about 6 weeks at 2-8°C as an undiluted liquid.Extended Storage after Rehydration: Aliquot and freeze at -70°C or below. Avoid repeated freezing and thawing. Alternatively, add an equal volume of glycerol (ACS grade or better) for a final concentration of 50%, and store at -20°C as a liquid. Expiration date: one year from date of rehydration. The expiration date may be extended if test results are acceptable for the intended use.

      Purity:The IgG fraction was purified from mouse ascites by chromatographic procedures not involving affinity purification. Buffer: 0.01M Sodium Phosphate, 0.25M NaCl, pH 7.6 Stabilizer:15 mg/ml Bovine Serum Albumin (IgG-Free, Protease-Free) Preservative:0.05% Sodium Azide Conjugate

      Coumarin AMCA

      Amax: 350Emax: 450nm

      Aminomethylcoumarin Acetate (AMCA) conjugates absorb light maximally around 350 nm and fluoresce maximally around 450 nm. For fluorescence microscopy, AMCA can be excited with a mercury lamp and observed using a UV filter set. Since blue fluorescence is not well detected by the human eye, AMCA-conjugated secondary antibodies should be used only with the most abundant antigens in multiple-labeling experiments. Ways of improving the visibility of AMCA include dark adapting the eyes, using fluorite instead of glass objectives, avoiding mounting media that absorb UV light (such as plastic-based media), and capturing photographic images with blue-sensitive film or CCD cameras. AMCA fades rapidly in conventional epifluorescence and confocal microscopy, and therefore it should be used with mounting media containing an anti-fading agent such as n-propyl gallate.

      Images & References

      This product is for in vitro research use only. It is not a medical device and it is not intended for diagnostic or therapeutic purposes.

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