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Primary antibodies against cd63 and tsg101

Manufactured by Abcam
Sourced in United Kingdom

Primary antibodies against CD63 and TSG101 are used to detect the presence and levels of these proteins in biological samples. CD63 is a membrane protein involved in exosome biogenesis, while TSG101 is a protein that plays a role in the formation of multivesicular bodies. These antibodies can be used in various techniques, such as Western blotting, immunohistochemistry, and flow cytometry, to study the expression and localization of these proteins.

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3 protocols using primary antibodies against cd63 and tsg101

1

Exosome Marker Identification Protocol

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To identify exosome markers, we purchased primary antibodies against CD63 and TSG101 from Abcam (Cambridge, UK), and primary antibodies against Hsp 70 and Hsp 90 were obtained from Cell Signaling Technology (CST, Beverly, MA, USA). The secondary antibodies were F(ab)2 fragments of donkey anti-mouse immunoglobulin or donkey anti-rabbit immunoglobulin linked to horseradish peroxidase (Jackson ImmunoResearch, USA). Immunoblotting reagents from an electrochemiluminescence kit were used (Amersham Biosciences, Uppsala, Sweden).
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2

Exosome Marker Identification Protocol

Check if the same lab product or an alternative is used in the 5 most similar protocols
To identify exosome markers, primary antibodies against CD63 and TSG101 were purchased from Abcam (Cambridge, UK), and primary antibodies against Hsp 70 and Hsp 90 were obtained from Cell Signaling Technology (Beverly, MA, USA). The secondary antibodies were F(ab)2 fragments of donkey anti-mouse immunoglobulin or donkey anti-rabbit immunoglobulin linked to horseradish peroxidase (Jackson ImmunoResearch Laboratories, USA). Immunoblotting reagents from an electrochemiluminescence kit were used (Amersham Biosciences, Uppsala, Sweden).
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3

Exosome Protein Marker Detection

Check if the same lab product or an alternative is used in the 5 most similar protocols
To identify exosome markers, primary antibodies against CD63 and TSG101 were purchased from Abcam (Cambridge, UK), and primary antibodies against Hsp 70 and Hsp 90 were obtained from Cell Signaling Technology (CST, Beverly, MA, USA). The secondary antibodies were F(ab)2 fragments of donkey anti-mouse immunoglobulin or donkey anti-rabbit immunoglobulin linked to horseradish peroxidase (Jackson ImmunoResearch, Inc., USA). Immunoblotting reagents from an electrochemiluminescence kit were used (Amersham Biosciences, Uppsala, Sweden).
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