Ki67 Recombinant Rabbit Monoclonal Antibody

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- 20μL
- ¥620
- 1-3个工作日
-
- 50μL
- ¥1250
- 1-3个工作日
-
- 100μL
- ¥2200
- 1-3个工作日
Product Details | Host Species: Rabbit | Reactivity: Human,Mouse,Rat | Molecular Wt: Predicted MW: 359 kDa | |||
| Clonality: Monoclonal | Isotype: IgG | Concentration: 1.065mg/ml | |||
| Other Names: Antigen KI 67; Antigen KI-67; Antigen Ki67; Ki 67; KI67; KIA; MKI67; MIB; MIB 1; Antigen identified by monoclonal antibody Ki 67; Antigen identified by monoclonal antibody Ki-67; PPP1R105; Proliferation marker protein Ki-67; Proliferation related Ki 67 antigen | |||||
| Formulation: Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide. | |||||
| Purification: Affinity-chromatography | |||||
| Storage: Store at -20°C. Stable for one year after shipment. Aliquoting is unnecessary for -20°C storage. | |||||
Applications | WB 1:500-1:2000 | |||||
Immunogen | Gene Name: MKI67 | Protein Name: Proliferation marker protein Ki-67 | ||||
| Gene ID: 4288 (Human) | SwissPro: P46013 (Human) | ||||
| Subcellular Location: Chromosome. Nucleus. Nucleus, nucleolus. | |||||
| Immunogen: Synthetic peptide within human Ki67. AA range: 1040-1080. | |||||
| Specificity: Ki67 Monoclonal Antibody detects endogenous levels of Ki67 protein. |
Product images | |
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Fig: Multiplex immunohistochemistry analysis of Mouse-spleen tissue (Formalin/PFA-fixed paraffin-embedded sections). Merged staining of anti-Ki67 (AWA10320; green; TSA-520:AWI0688), anti-AGMAT (AWA54578; red; TSA-570: AWI0689), anti-CD20 (AWA10037; white; TSA-690: AWI0691). Antibody Wash Solution (for mIHC) (AWI0707, 37℃, 20 minutes) was used in between rounds of tyramide signal amplification to remove the antibody from the previous round, to avoid any cross-reactivity. The section was incubated in three rounds of staining; in the order of Ki67 (AWA10320) (1/800 dilution), anti-AGMAT (AWA54578) (1/200 dilution), anti-CD20 (AWA10037) (1/200 dilution); each using a separate fluorescent tyramide signal amplification system. DAPI (blue, AWC0291) was used as a nuclear counter stain. Microscopy and pseudocoloring of individual TSA dyes was performed using a pannoramic midi. This image was generated from the hybridoma version. |
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Fig : Western blot analysis of Ki67 on different lysates. Proteins were transferred to a NC membrane and blocked with 5% NF-Milk in TBST for 1 hour at room temperature. The primary antibody (AWA10320, 1/1000) was used in TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody (AWS0002) at 1:5,000 dilution was used for 1 hour at room temperature. Positive control: Lane 1: A431 cell Lane 2: A549 cell Lane 3: SIHa cell Lane 4: HepG2 cell Lane 5: CAL27 cell Lane 6: MCF-7 cell Lane 7: Raji cell Lane 8: HaCaT cell Lane 9: PANC-1 cell Predicted molecular weight:359 kDa Observed molecular weight:359 kDa |
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Fig : Western blot analysis of Ki67 on different lysates. Proteins were transferred to a NC membrane and blocked with 5% NF-Milk in TBST for 1 hour at room temperature. The primary antibody (AWA10320, 1/1000) was used in TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody (AWS0002) at 1:5,000 dilution was used for 1 hour at room temperature. Positive control: Lane 1: SIHa cell Lane 2: EL-4-B5 cell Predicted molecular weight:359 kDa Observed molecular weight:359 kDa |
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Fig: Immunocytochemistry analysis of U2SO cells labeling Ki67 with Rabbit anti-Ki67 antibody (AWA10320) at 1/50 dilution(green). Cells were fixed in 4% paraformaldehyde for 10 minutes at 37 ℃, permeabilized with 0.03% Triton X-100 in PBS for 30 minutes, and then blocked with 5% BSA for 60 minutes at 37 ℃. Cells were then incubated with Rabbit anti-Ki67 antibody (AWA10320) at 1/50 dilution in 2% negative goat serum overnight at 4 ℃. Goat Anti-Rabbit IgG H&L (iFluor™488, AWS0005) was used as the secondary antibody at 1/200 dilution for 60 minutes at 37 ℃. Nuclear DNA was labelled in blue with DAPI(AWC0291). |
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Fig : Immunohistochemical analysis of paraffin-embedded Mouse-large intestine tissue with Rabbit anti-Ki67 antibody (AWA10320) at 1/200 dilution. The section was pre-treated using heat mediated antigen retrieval with Sodium citrate buffer (pH 6.0) for 20 minutes. The tissues were blocked in 3% H2O2 for 15 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (AWA10320) at 1/200 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system(ABIOWELL, AWI0629). DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX. |
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Fig : Immunohistochemical analysis of paraffin-embedded Mouse-heart tissue with Rabbit anti-KI67 (AWA10320) at 1/800 dilution. The section was pre-treated using heat mediated antigen retrieval with Sodium citrate buffer (pH 6.0) for 20 minutes. The tissues were blocked in 3% H2O2 for 15 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (AWA10320) at 1/800 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system(ABIOWELL, AWI0629). DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX. |
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Fig : Immunohistochemical analysis of paraffin-embedded Rat-heart tissue with Rabbit anti-KI67 (AWA10320) at 1/800 dilution. The section was pre-treated using heat mediated antigen retrieval with Sodium citrate buffer (pH 6.0) for 20 minutes. The tissues were blocked in 3% H2O2 for 15 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (AWA10320) at 1/800 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system(ABIOWELL, AWI0629). DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX. |
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Fig : Immunohistochemical analysis of paraffin-embedded rat-testicle tissue with Rabbit anti-Ki67 (AWA10320) at 1/100 dilution. The section was pre-treated using heat mediated antigen retrieval with Sodium citrate buffer (pH 6.0) for 20 minutes. The tissues were blocked in 3% H2O2 for 15 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (AWA10320) at 1/100 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system(ABIOWELL, AWI0629). DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX. |
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Fig : Immunohistochemical analysis of paraffin-embedded rat-spleen tissue with Rabbit anti-Ki67 (AWA10320) at 1/100 dilution. The section was pre-treated using heat mediated antigen retrieval with Sodium citrate buffer (pH 6.0) for 20 minutes. The tissues were blocked in 3% H2O2 for 15 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (AWA10320) at 1/100 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system(ABIOWELL, AWI0629). DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX. |
1. Peng, Ying et al. “S100A2 upregulates GLUT1 expression to promote glycolysis in the progression of nasopharyngeal carcinoma.” Histology and histopathology vol. 39,12 (2024): 1669-1683. doi:10.14670/HH-18-778. PubMed:38940398
2. Li, Wei et al. “4,5-Dimethoxycanthin-6-one Inhibits Glioblastoma Stem Cell and Tumor Growth by Inhibiting TSPAN1 Interaction with TM4SF1.” Neurochemical research vol. 49,10 (2024): 2897-2909. doi:10.1007/s11064-024-04211-y. PubMed:39060768
3. Lin, Long et al. “Nrf2 activator tertiary butylhydroquinone enhances neural stem cell differentiation and implantation in Alzheimer's disease by boosting mitochondrial function.” Brain research vol. 1849 (2025): 149341. doi:10.1016/j.brainres.2024.149341. PubMed:39566569
-
-
- 20μL
- ¥620
- 1-3个工作日
-
- 50μL
- ¥1250
- 1-3个工作日
-
- 100μL
- ¥2200
- 1-3个工作日
-
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