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- Table of Contents
PIK3R1 antibody (A00318-1) performs well in ELISA, Flow Cytometry, IF, IHC, ICC, WB and shows reactivity with Human, Mouse, Rat.
| Reactive Species | Host | Application |
|---|---|---|
| Human, Mouse, Rat | Rabbit | ELISA, Flow Cytometry, IF, IHC, ICC, WB |
PIK3R1 antibody was positively detected by WB in:
human Jurkat whole cell, human Hela whole cell, rat PC-12 whole cell, mouse RAW2647 whole cell
Suggested blocking solution with 5% non-fat milk or BSA; (*)Recommended protein loading: 20-40 ug per lane
PIK3R1 antibody was positively detected by IHC in:
human lung cancer tissue, human lymphoma tissue, human testicular cancer tissue, mouse brain tissue, rat brain tissue
Use TE buffer pH 9.0 for antigen retrieval; (*) citrate buffer pH 6.0 is an alternative.
PIK3R1 antibody was positively detected by ICC/IF in:
Caco-2 cell
PIK3R1 antibody was positively detected by FC in:
HL-60 cell
* It is recommended to optimize the amount of this reagent in each experimental system to achieve the best results.
Note: For flow cytometry (FCM), suitable for fixed cells only. Not suitable for FACS or surface flow cytometry using live cells.
83.6 kDa
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| SKU | A00318-1 |
|---|---|
| Application | Western Blot |
| Sample | Mouse brain tissue |
| Sample Processing Description | Mouse brain tissue was lysed in RIPA buffer supplemented with protease inhibitors at 4°C for 2 hours. The lysate was centrifuged to collect the supernatant, and protein concentration was determined. After adjusting the concentration, samples were mixed with 5× protein loading buffer and heated at 95–100°C for 10 minutes to denature. Then, 15 μL of each protein sample was loaded per lane for electrophoresis. |
| Other Reagents | Blocking buffer |
| Primary Antibody | PI 3 Kinase p85 alpha/PIK3R1 Antibody Picoband® |
| Primary Incubation | 1:2000, overnight at 4 ℃ |
| Secondary Antibody | HRP Goat Anti-Rabbit IgG |
| Secondary Incubation | 1:10000, 1 hour in room temperature |
| Detection | Substrate: ECL, Imaging system:ChemiDoc MP |
| Results Summary | The figure shows a schematic representation of Western blot results for PIK3R1 and the loading control β-actin in mouse brain tissues from normal mice, model group, and mice treated with high and low doses of drug AB. Although the expression differences between experimental groups are not pronounced, the Western blot results obtained with this antibody are still clear and well-defined. |
Yetao Ju, Liaoning Univ. of TCM
Verified customer
Submitted 2025-12-25

| SKU | A00318-1 |
|---|---|
| Application | Western Blot |
| Sample | Mouse hippocampus tissue |
| Sample Processing Description | The mouse hippocampus was lysed with RIPA lysis buffer containing protease inhibitors, followed by protein quantification. The samples were then mixed with 5× protein loading buffer and heated for 10 minutes for denaturation. Five microliters of protein sample were loaded into each lane for SDS-PAGE. |
| Primary Antibody | Anti-PI 3 Kinase p85 alpha/PIK3R1 Antibody Picoband® |
| Primary Incubation | overnight at 4 ℃ |
| Secondary Antibody | HRP-conjugated Anti-Rabbit IgG Secondary Antibody |
| Secondary Incubation | 1 hour in room temperature |
| Detection | Substrate: Ultra-sensitive ECL luminescent reagent , Imaging system:ChemiDoc MP |
| Results Summary | The antibody shows clear bands with no non-specific signals in WB, and is suitable for detecting PIK3R1 protein in mouse hippocampus by Western blot. |
Yali Yang, LNUTCM
Verified customer
Submitted 2025-11-10
We promise Anti-PI 3 Kinase p85 alpha/PIK3R1 Antibody Picoband® performs excellently in relevant applications for ELISA, Flow Cytometry, IF, IHC, ICC, WB. If it doesn't perform as promised, we will refund the product. Learn more
We promise all of our products perform as described in datasheets.
This product is for Research Use Only. Not for use in diagnostic procedures.