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Alexa fluor 488 anti igg

Manufactured by Thermo Fisher Scientific
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Sourced in Japan

Alexa Fluor 488 anti-IgG is a fluorescently labeled secondary antibody that binds to immunoglobulin G (IgG) antibodies. It is designed for use in various immunoassay and cellular imaging applications.

Automatically generated - may contain errors

Lab products found in correlation

Ix81 fluorescence microscope, by Olympus (1 mentions) Blocking one, by Nacalai Tesque (1 mentions)

Close spelling variants of this product

Alexa Fluor 488 anti-mouse and 568 anti-rabbit IgGs Alexa fluor 488 conjugated anti-mouse IgG (H+L) Alexa Fluor 488 or 633 goat anti-mouse IgG Alexa Fluor 488 goat anti-mouse immunoglobulin G (IgG) (H+L) Alexa Fluor 488-conjugated goat anti-rat IgG antibody Alexa Fluor 488-labeled goat anti-mouse IgG Alexa Fluor 488-conjugated anti-mouse immunoglobulin G (IgG), Alexa Fluor 488-tagged donkey anti-mouse IgG Alexa Fluor® 488 conjugated Donkey Anti-Rabbit IgG (H + L) antibody Anti-rabbit IgG Alexa Fluor 488 conjugate

2 protocols using alexa fluor 488 anti igg

1

Pluripotency Marker Expression in hiPSCs

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hiPSC colonies were fixed in paraformaldehyde and permeabilized in Triton X-100 prior to Oct4 and Nanog staining. Cells were then stained with secondary antibody Alexa Fluor 488 anti- IgG (Molecular Probes). DAPI staining was performed to visualize the nucleus (Molecular probes). Cells were visualized using the Olympus IX81 fluorescence microscope and images were captured with using the Q Capture software.
Rao R.A., Dhele N., Cheemadan S., Ketkar A., Jayandharan G.R., Palakodeti D, & Rampalli S. (2015). Ezh2 mediated H3K27me3 activity facilitates somatic transition during human pluripotent reprogramming. Scientific Reports, 5, 8229.
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2

Immunofluorescent labeling of α-internexin

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The fixation of culture cells was performed in 0.1% glutaraldehyde containing phosphate saline buffer (pH 7.4). This was followed by blocking with Blocking One (Nacalai Tesque) and an incubation with the anti-α-internexin antibody (1:500, Abcam, Tokyo, Japan, ab10830) and then with Alexa Fluor 488 anti-IgG (Molecular Probes, Eugene, OR, United States).
Ooi H., Nasu R., Furukawa A., Takeuchi M, & Koriyama Y. (2022). Pyridoxamine and Aminoguanidine Attenuate the Abnormal Aggregation of β-Tubulin and Suppression of Neurite Outgrowth by Glyceraldehyde-Derived Toxic Advanced Glycation End-Products. Frontiers in Pharmacology, 13, 921611.
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