full length srpk2 (Carna Inc)
Carna Inc is a verified supplier 
Carna Inc manufactures this product 
96
Structured Review
Carna Inc
full length srpk2
Full Length Srpk2, supplied by Carna Inc, used in various techniques. Bioz Stars score: 96/100, based on 2 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/04-161/SRPK2/pmc04762521-74-105-114
Average 96 stars, based on 2 article reviews
Full Length Srpk2, supplied by Carna Inc, used in various techniques. Bioz Stars score: 96/100, based on 2 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/04-161/SRPK2/pmc04762521-74-105-114
Average 96 stars, based on 2 article reviews
full length srpk2 - by Bioz Stars,
2026-09
96/100 stars
Images
Related Articles
De-Phosphorylation Assay:Article Title: Uncovering Phosphorylation-Based Specificities through Functional Interaction Networks Article Snippet: .. Dephosphorylation was then carried out with TSAP (Promega, Madison, MI, USA) at 37 °C for 1 h, and TSAP was inactivated by heating to 75 °C for 30 min. For in vitro kinase reaction, each 100 g of dephosphorylated proteins (1 g/ l) was reacted with 1 l of each recombinant kinase (0.5 g/ l) or distilled water as a control at 37 °C in kinase reaction buffer (40 mM Tris-HCl (pH 7.5), 20 mM MgCl2, 1 mM ATP) for 3 h. AKT2, catalytic domain [120–481(end), accession NP_001617.1], full-length EIF2AK4 [1–1649(end) accession Q9P2K8.2], full-length HIPK2 [1–1198(end) accession Q9H2X6] and Molecular & Cellular Proteomics 15.1 237 Article Title: Uncovering Phosphorylation-Based Specificities through Functional Interaction Networks Article Snippet: .. Dephosphorylation was then carried out with TSAP (Promega, Madison, MI, USA) at 37 °C for 1 h, and TSAP was inactivated by heating to 75 °C for 30 min. For in vitro kinase reaction, each 100 μg of dephosphorylated proteins (1 μg/μl) was reacted with 1 μl of each recombinant kinase (0.5 μg/μl) or distilled water as a control at 37 °C in kinase reaction buffer (40 m m Tris-HCl (pH 7.5), 20 m m MgCl 2 , 1 m m ATP) for 3 h. AKT2, catalytic domain [120–481(end), accession NP_001617.1 ], full-length EIF2AK4 [1–1649(end) accession Q9P2K8 .2], full-length HIPK2 [1–1198(end) accession Q9H2X6 ] and In Vitro:Article Title: Uncovering Phosphorylation-Based Specificities through Functional Interaction Networks Article Snippet: .. Dephosphorylation was then carried out with TSAP (Promega, Madison, MI, USA) at 37 °C for 1 h, and TSAP was inactivated by heating to 75 °C for 30 min. For in vitro kinase reaction, each 100 g of dephosphorylated proteins (1 g/ l) was reacted with 1 l of each recombinant kinase (0.5 g/ l) or distilled water as a control at 37 °C in kinase reaction buffer (40 mM Tris-HCl (pH 7.5), 20 mM MgCl2, 1 mM ATP) for 3 h. AKT2, catalytic domain [120–481(end), accession NP_001617.1], full-length EIF2AK4 [1–1649(end) accession Q9P2K8.2], full-length HIPK2 [1–1198(end) accession Q9H2X6] and Molecular & Cellular Proteomics 15.1 237 Article Title: Uncovering Phosphorylation-Based Specificities through Functional Interaction Networks Article Snippet: .. Dephosphorylation was then carried out with TSAP (Promega, Madison, MI, USA) at 37 °C for 1 h, and TSAP was inactivated by heating to 75 °C for 30 min. For in vitro kinase reaction, each 100 μg of dephosphorylated proteins (1 μg/μl) was reacted with 1 μl of each recombinant kinase (0.5 μg/μl) or distilled water as a control at 37 °C in kinase reaction buffer (40 m m Tris-HCl (pH 7.5), 20 m m MgCl 2 , 1 m m ATP) for 3 h. AKT2, catalytic domain [120–481(end), accession NP_001617.1 ], full-length EIF2AK4 [1–1649(end) accession Q9P2K8 .2], full-length HIPK2 [1–1198(end) accession Q9H2X6 ] and Recombinant:Article Title: Uncovering Phosphorylation-Based Specificities through Functional Interaction Networks Article Snippet: .. Dephosphorylation was then carried out with TSAP (Promega, Madison, MI, USA) at 37 °C for 1 h, and TSAP was inactivated by heating to 75 °C for 30 min. For in vitro kinase reaction, each 100 g of dephosphorylated proteins (1 g/ l) was reacted with 1 l of each recombinant kinase (0.5 g/ l) or distilled water as a control at 37 °C in kinase reaction buffer (40 mM Tris-HCl (pH 7.5), 20 mM MgCl2, 1 mM ATP) for 3 h. AKT2, catalytic domain [120–481(end), accession NP_001617.1], full-length EIF2AK4 [1–1649(end) accession Q9P2K8.2], full-length HIPK2 [1–1198(end) accession Q9H2X6] and Molecular & Cellular Proteomics 15.1 237 Article Title: Uncovering Phosphorylation-Based Specificities through Functional Interaction Networks Article Snippet: .. Dephosphorylation was then carried out with TSAP (Promega, Madison, MI, USA) at 37 °C for 1 h, and TSAP was inactivated by heating to 75 °C for 30 min. For in vitro kinase reaction, each 100 μg of dephosphorylated proteins (1 μg/μl) was reacted with 1 μl of each recombinant kinase (0.5 μg/μl) or distilled water as a control at 37 °C in kinase reaction buffer (40 m m Tris-HCl (pH 7.5), 20 m m MgCl 2 , 1 m m ATP) for 3 h. AKT2, catalytic domain [120–481(end), accession NP_001617.1 ], full-length EIF2AK4 [1–1649(end) accession Q9P2K8 .2], full-length HIPK2 [1–1198(end) accession Q9H2X6 ] and Control:Article Title: Uncovering Phosphorylation-Based Specificities through Functional Interaction Networks Article Snippet: .. Dephosphorylation was then carried out with TSAP (Promega, Madison, MI, USA) at 37 °C for 1 h, and TSAP was inactivated by heating to 75 °C for 30 min. For in vitro kinase reaction, each 100 g of dephosphorylated proteins (1 g/ l) was reacted with 1 l of each recombinant kinase (0.5 g/ l) or distilled water as a control at 37 °C in kinase reaction buffer (40 mM Tris-HCl (pH 7.5), 20 mM MgCl2, 1 mM ATP) for 3 h. AKT2, catalytic domain [120–481(end), accession NP_001617.1], full-length EIF2AK4 [1–1649(end) accession Q9P2K8.2], full-length HIPK2 [1–1198(end) accession Q9H2X6] and Molecular & Cellular Proteomics 15.1 237 Article Title: Uncovering Phosphorylation-Based Specificities through Functional Interaction Networks Article Snippet: .. Dephosphorylation was then carried out with TSAP (Promega, Madison, MI, USA) at 37 °C for 1 h, and TSAP was inactivated by heating to 75 °C for 30 min. For in vitro kinase reaction, each 100 μg of dephosphorylated proteins (1 μg/μl) was reacted with 1 μl of each recombinant kinase (0.5 μg/μl) or distilled water as a control at 37 °C in kinase reaction buffer (40 m m Tris-HCl (pH 7.5), 20 m m MgCl 2 , 1 m m ATP) for 3 h. AKT2, catalytic domain [120–481(end), accession NP_001617.1 ], full-length EIF2AK4 [1–1649(end) accession Q9P2K8 .2], full-length HIPK2 [1–1198(end) accession Q9H2X6 ] and |