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- Table of Contents
Il6 antibody (PA1352) performs well in IHC, WB and shows reactivity with Mouse, Rat.
| Reactive Species | Host | Application |
|---|---|---|
| Mouse, Rat | Rabbit | IHC, WB |
Il6 antibody was positively detected by WB in:
recombinant rat IL6 protein, mouse spleen tissue, rat thymus tissue, rat spleen tissue
Suggested blocking solution with 5% non-fat milk or BSA; (*)Recommended protein loading: 20-40 ug per lane
Il6 antibody was positively detected by IHC in:
rat spleen tissue
Use TE buffer pH 9.0 for antigen retrieval; (*) citrate buffer pH 6.0 is an alternative.
* It is recommended to optimize the amount of this reagent in each experimental system to achieve the best results.
24.4 kDa
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| SKU | PA1352 |
|---|---|
| Application | Western Blot |
| Sample | PC-12 (rat adrenal pheochromocytoma cells, highly differentiated) |
| Sample Processing Description | ① Normal PC12 cells (rat adrenal pheochromocytoma cells, highly differentiated)② PC12 cells are treated with β-amyloid (Aβ) to establish an in vitro Alzheimer's disease (AD) model.③ The AD in vitro model is treated with the therapeutic drug. |
| Other Reagents | RIPA lysis buffer, Protease inhibitor, Electrophoresis buffer, Transfer buffer, Blocking buffer |
| Primary Antibody | Interleukin-6 IL6 Antibody Picoband® |
| Primary Incubation | 1:2500, overnight at 4 ℃ |
| Secondary Antibody | HRP-conjugated goat anti-rabbit IgG |
| Secondary Incubation | 1:10000, 1 hour in RT |
| Detection | Substrate: ECL substrate; Image system: ChemiDoc MP |
| Results Summary | ① Normal PC-12 cells (rat adrenal pheochromocytoma cells (highly differentiated)) ② PC12 cells were induced with β-amyloid protein (Aβ) to establish an in vitro model of Alzheimer's disease (AD) ③ The AD in vitro model was treated with therapeutic drugs. Experimental results showed clear target bands. After modeling, the total expression level of MAPK14 protein was upregulated, and the expression level decreased after drug treatment, which was in line with expectations. |
Yue Zhang, Chengdu University of Traditional Chinese Medicine
Verified customer
Submitted 2026-08-26

| SKU | PA1352 |
|---|---|
| Application | Western Blot |
| Sample | Human mcf-7 cells |
| Sample Processing Description | RIPA lysis buffer supplemented with a protease inhibitor cocktail was added to the cell culture dish, and the cells were lysed on ice for 30 min. The lysates were then centrifuged, and the supernatants were collected. Protein concentration was determined, and samples were adjusted to equal concentrations. Subsequently, 5× protein loading buffer was added, and the samples were denatured at 100 °C for 10 min. A total of 15 μL of protein sample was loaded per lane for SDS-PAGE electrophoresis. |
| Other Reagents | Blocking buffer |
| Primary Antibody | CRCP Rabbit Monoclonal Antibody |
| Primary Incubation | 1:2000, overnight at 4 ℃ |
| Secondary Antibody | HRP Conjugated AffiniPure Goat Anti-Rabbit IgG (H+L) |
| Secondary Incubation | 1 hour in room temperature |
| Detection | Substrate: ECL, Imaging system:ChemiDoc MP |
| Results Summary | As shown in the figure, the expression levels of CRCP protein in MCF-7 cells at different drug treatment time points are presented. The Western blot results obtained with this antibody are clear; although there are a few faint nonspecific bands above, they do not affect result interpretation. It can be observed that the expression of the target protein in MCF-7 cells increases with longer drug treatment times. |
Siyuan Bu, LUTCM
Verified customer
Submitted 2025-12-26
We promise Anti-Interleukin-6 IL6 Antibody Picoband® performs excellently in relevant applications for IHC, 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.