HEXIM1 (AAH06460, 1 a.a. ~ 360 a.a) full-length recombinant protein with GST tag. MW of the GST tag alone is 26 KDa.
Conjugate
Unconjugated
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IHC-P analysis of placenta tissue by HEXIM1 antibody. IHC-P was performed using sections of the formalin-fixed paraffin-embedded placenta tissue. Antigen was retrieved through addition of boiling Tris/EDTA buffer pH 9 in a pressure cooker for 3 min. Endogenous peroxidase activity was quenched by incubating the sections with 3% H2O2 for 30 min at room temperature. The sections were then incubated with HEXIM1 antibody at 7.5 µg/mL at room temperature for 1 h. Poly-peroxidase conjugated goat anti-mouse IgG was used as the secondary antibody. Diaminobenzidine was used as the chromogen. The section was counterstained with hematoxylin. A tissue section incubated with phosphate-buffered saline followed by incubation with the secondary antibody was used as the background control. Result: Decidual cells and trophoblastic cells are positively stained at the nuclei and cytoplasm.
Expression of this gene is induced by hexamethylene-bis-acetamide in vascular smooth muscle cells. This gene has no introns. Mouse monoclonal antibody raised against a full-length recombinant HEXIM1.
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Citations
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Krueger, BJ; Varzavand, K; et al. The Mechanism of Release of P-TEFb and HEXIM1 from the 7SK snRNP by Viral and Cellular Activators Includes a Conformational Change in 7SK. PLOS ONE 5:-(2010).
Breuer, D; Kotelkin, A; et al. CDK2 Regulates HIV-1 Transcription by Phosphorylation of CDK9 on Serine 90. RETROVIROLOGY 9:-(2012).
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Anti-HEXIM1 monoclonal antibody
IHC-P analysis of placenta tissue by HEXIM1 antibody. IHC-P was performed using sections of the formalin-fixed paraffin-embedded placenta tissue. Antigen was retrieved through addition of boiling Tris/EDTA buffer pH 9 in a pressure cooker for 3 min. Endogenous peroxidase activity was quenched by incubating the sections with 3% H2O2 for 30 min at room temperature. The sections were then incubated with HEXIM1 antibody at 7.5 µg/mL at room temperature for 1 h. Poly-peroxidase conjugated goat anti-mouse IgG was used as the secondary antibody. Diaminobenzidine was used as the chromogen. The section was counterstained with hematoxylin. A tissue section incubated with phosphate-buffered saline followed by incubation with the secondary antibody was used as the background control. Result: Decidual cells and trophoblastic cells are positively stained at the nuclei and cytoplasm.
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