Slide Mounting Media
Electron Microscopy Sciences Citifluor™ Mountant Solution CFM-2, Glycerol Based, Non Hardening 25 ML
Citifluor mounting medium for immunofluorescence is designed to reduce the fading of the fluorescence of dyes used for labeling biological specimens. In the technique of fluorescence microscopy, the fluorescence is stimulated by high intensity UV and/or visible light. Absorption of the light populates an excited state of the dye (usually a singlet state) and this leads to fluorescence. However, the excited state of the dye may undergo chemical reaction, which leads to destruction as evidenced by the fading of the fluorescence and consequent loss of the image. Glycerol-tris amine buffered solution with a refractive index of ~1.52. pH 8.5.
Material: Glycerol Based
Type: Non Hardening
Electron Microscopy Sciences Citifluor™ Mountant Solution CFM-1, Glycerol Based, Non Hardening 25 ML
Citifluor mounting medium for immunofluorescence is designed to reduce the fading of the fluorescence of dyes used for labeling biological specimens. In the technique of fluorescence microscopy, the fluorescence is stimulated by high intensity UV and/or visible light. Absorption of the light populates an excited state of the dye (usually a singlet state) and this leads to fluorescence. However, the excited state of the dye may undergo chemical reaction, which leads to destruction as evidenced by the fading of the fluorescence and consequent loss of the image. Glycerol-PBS buffered solution with a refractive index of ~1.52. For TEM or epi-fluorescence.
Material: Glycerol Based
Type: Non Hardening
Electron Microscopy Sciences Citifluor™ Mountant Solution PVP-1, Glycerol Free, Hardening 25 ML
Citifluor mounting medium for immunofluorescence is designed to reduce the fading of the fluorescence of dyes used for labeling biological specimens. In the technique of fluorescence microscopy, the fluorescence is stimulated by high intensity UV and/or visible light. Absorption of the light populates an excited state of the dye (usually a singlet state) and this leads to fluorescence. However, the excited state of the dye may undergo chemical reaction, which leads to destruction as evidenced by the fading of the fluorescence and consequent loss of the image. Aqueous solution of poly(vinyl pyrrolidone).
Material: Glycerol Free
Type: Hardening
Rowley Biochemical Institute Inc ACETIC ACID 0.2 AQUEOUS 1 QT
NC3432185 ACETIC ACID 0.2 AQUEOUS 1 QT
Electron Microscopy Sciences SEM Hitachi S-450 M4 Mount Plain Surface 5/8",1/4" height, Aluminum
Hitachi S-450 SEM mounts with M4 tapered hole and female thread. Made from ultra-pure aluminum with standard lathe finish.
Head: 5/8"
Height: 1/4"
Enzo Life Sciences HIGHDEF IHC enhancer (DAB, plus) (15ml)
The HIGHDEF IHC enhancer (DAB, plus) is a DAB signal enhancer that can be used to increase intensity of immunostaining utilizing DAB as chromogen. Formulation: Liquid. 1X DAB chromogen enhancer. Appearance: Amber solution. Long Term Storage: Ambient. Applications: IHC .
BIOHIPPO AAV-hSyn-DIO-mito-EGFP-P2A-tdTomato-WPRE-hGH-polyA
Recombinant adeno associated virus expressing EGFP mito-EGFP tdTomato under the hSyn promoter with WPRE and hGH polyA elements. The Cre dependent configuration enables expression only after recombination, providing precise targeted control of targeted neurons. Offered under the Biohippo AAVX Series with multiple serotypes available including AAV2/1, AAV2/2, AAV2/5, AAV2/6, AAV2/6m, AAV2/6.2FF, AAV2/7m8, AAV2/8, AAV2/9, AAV2/DJ, AAV2/DJ8, AAV2/Retro, AAV2/PHP.eB, AAV2/PHP.B, AAV2/rh10, AAV2/PHP.S, AAV2/anc80, AAV2/B10, AAV2/olig001, AAV2/BI30, AAV2/BR1, AAV2/MG1.2, AAV1/2, AAV2/MaCPNS1, and AAV2/MaCPNS2. Regular titer is greater than or equal to 2.00E+12 vg per mL, with high titer greater than or equal to 1.00E+13 vg per mL available upon request at no additional cost. Customers may specify preferred serotype and titer when placing orders.
Electron Microscopy Sciences Citifluor™ Mountant Solution AF3, Glycerol Free, Non Hardening 25 ML
Citifluor mounting medium for immunofluorescence is designed to reduce the fading of the fluorescence of dyes used for labeling biological specimens. In the technique of fluorescence microscopy, the fluorescence is stimulated by high intensity UV and/or visible light. Absorption of the light populates an excited state of the dye (usually a singlet state) and this leads to fluorescence. However, the excited state of the dye may undergo chemical reaction, which leads to destruction as evidenced by the fading of the fluorescence and consequent loss of the image. PBS solution containing an amine-based antifadent.
Material: Glycerol Free
Type: Non Hardening
AdipoGen DAPI dihydrochloride
Chemical. CAS 28718-90-3. Formula C16H15N5 . 2HCl. MW 277.3 . 72.9. Synthetic. DAPI 4,6-Diamidino-2-phenylindole dihydrochloride is a cell permeable, fluorescent dye that is a minor groove-binding probe for DNA. Binds to the minor groove of double-stranded DNA preferentially to AT rich DNA, forming a stable complex which fluoresces approximately 20 times greater than DAPI alone. DAPI is several times more sensitive than ethidium bromide for staining DNA in agarose gels. It may be used for photofootprinting of DNA, to detect annealed probes in blotting applications by specifically visualizing the double-stranded complex, and to study the changes in DNA and analyze DNA content during apoptosis using flow cytometry. DAPI staining has also been shown to be a sensitive and specific detection method for mycoplasma. Spectral Data Excitation lambdaex 340 nm Emission lambdaem 488 nm only DAPI. Excitation lambdaex 360nm Emission lambdaem 460nm DAPI-DNA complex.
