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Snail ha

Manufactured by Addgene

The Snail-HA is a lab equipment product that serves as an epitope tag for protein expression and detection. It is a small, genetically encoded tag derived from the protein Snail, which can be fused to a target protein to enable its identification and purification using antibodies specific to the HA epitope.

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2 protocols using snail ha

1

Silencing TEAD and SNAIL/SLUG genes

Check if the same lab product or an alternative is used in the 5 most similar protocols
Human or mouse TEF-1, TEF-3, TEF-4 and TEF-5 (TEAD1–4) siRNAs, and human SNAIL or SLUG siRNAs were obtained from Santa Cruz Technology. To silence gene expression, PepMute siRNA Transfection Reagent (SignaGen Laboratories) was used for all siRNAs transfection. Flag-Snail, Snail-HA, Slug-Myc, Flag-YAP, Flag-TAZ, and 8xGTIIC were obtained from Addgene. HA-Runx2 and 6xOSE reporter constructs were provided by G. Stein 16 (link). Snail, Slug, YAP and TAZ mutants were constructed by PCR. Where indicated, Flag-YAP and Flag-TAZ were cloned into pLentilox-IRS-GFP lentiviral vectors and used to transduce SSCs, with the expression of the exogenous proteins confirmed by Western blot. For gene transfection, COS-1 cells or osteoblast progenitors were transfected with Lipofectamine 2000 (Invitrogen). For reporter assays, COS-1 cells were transfected with expression vectors and either 8xGTIIC or 6xOSE reporters. Luciferase activity in cell lysates was determined as previously described 9 (link).
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2

Silencing TEAD and SNAIL/SLUG genes

Check if the same lab product or an alternative is used in the 5 most similar protocols
Human or mouse TEF-1, TEF-3, TEF-4 and TEF-5 (TEAD1–4) siRNAs, and human SNAIL or SLUG siRNAs were obtained from Santa Cruz Technology. To silence gene expression, PepMute siRNA Transfection Reagent (SignaGen Laboratories) was used for all siRNAs transfection. Flag-Snail, Snail-HA, Slug-Myc, Flag-YAP, Flag-TAZ, and 8xGTIIC were obtained from Addgene. HA-Runx2 and 6xOSE reporter constructs were provided by G. Stein 16 (link). Snail, Slug, YAP and TAZ mutants were constructed by PCR. Where indicated, Flag-YAP and Flag-TAZ were cloned into pLentilox-IRS-GFP lentiviral vectors and used to transduce SSCs, with the expression of the exogenous proteins confirmed by Western blot. For gene transfection, COS-1 cells or osteoblast progenitors were transfected with Lipofectamine 2000 (Invitrogen). For reporter assays, COS-1 cells were transfected with expression vectors and either 8xGTIIC or 6xOSE reporters. Luciferase activity in cell lysates was determined as previously described 9 (link).
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