Biotinylation Labelling Kit formatted 10 x 1mg

SKU
AR100089
Biotinylation Labelling Kit formatted 10 x 1mg
  $5,400.00
3 Days*
Specifications
Specifications
Product Data
Features
  • Can be used with up to 10 mg/ml (1%) BSA as a carrier protein
  • Reaction complete in as little as 10 minutes
  • Room temperature-stable active biotinylation reagent
  • Pre-measured active biotinylation reagent coated onto a tube surface
  • Completely scalable: conjugate anywhere from 0.1 to 1 gram IgG per reaction
  • Highly efficient Biotin incorporation
  • Purification not usually required
Overview Biotin labeling kit contains all the reagents needed to biotinylate the stated amount of IgG and includes a highly pure solution of 104 mg/ml BSA for final formulation.
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Description Biotinylation Labelling Kit formatted 10 x 1mg
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MicroRNA-124 expression in the brains of rats during early cerebral ischemia and reperfusion injury is associated with cell apoptosis involving STAT3
Zhang, Meng
Exp Ther Med (2019) 17 (4), 2870-2876 DOI: 10.3892/etm.2019.7220
AI Summary: OriGene's SPlink detection kit (cat. no. AR100089) was used to block tissue sections prior to immunohistochemical analysis of apoptosis-related proteins in this study.
Snippet: Then the sections were blocked in buffer with 10% goat serum from a SPlink detection kit (cat. no. AR100089;OriGene Technologies, Inc., Beijing, China) at room temperature for 15 min. Caspase-3, Bcl-2 and Bax primary antibodies (1:500 dilution) were added to the sections and incubated overnight at 4°C
MicroRNA‑124 expression in the brains of rats during early cerebral ischemia and reperfusion injury is associated with cell apoptosis involving STAT3
Zhang, Meng
Exp Ther Med (2019)
AI Summary: OriGene products, specifically the primary antibodies for caspase-3, Bcl-2, and Bax, were used in this study to detect and analyze apoptosis-related protein expression in rat brain tissue during cerebral ischemia and reperfusion injury.
Snippet: no. AR100089;OriGene Technologies, Inc., Beijing, China) at room temperature for 15 min. Caspase‑3, Bcl‑2 and Bax primary antibodies (1:500 dilution) were added to the sections and incubated overnight at 4˚C. The sections were washed with 0.01 M PBS for 3 min
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