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AB206633

Alexa Fluor® 488 Anti-Ki67 antibody [KI67]

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(7 Publications)

Mouse Monoclonal Ki67 antibody - conjugated to Alexa Fluor® 488. Suitable for ICC, Flow Cyt (Intra) and reacts with Human samples. Cited in 7 publications. Immunogen corresponding to Cell preparation containing MKI67 protein.

View Alternative Names

Proliferation marker protein Ki-67, Antigen identified by monoclonal antibody Ki-67, Antigen KI-67, Antigen Ki67, MKI67

3 Images
Flow Cytometry (Intracellular) - Alexa Fluor® 488 Anti-Ki67 antibody [KI67] (AB206633)
  • Flow Cyt (Intra)

Supplier Data

Flow Cytometry (Intracellular) - Alexa Fluor® 488 Anti-Ki67 antibody [KI67] (AB206633)

Surface staining of PHA-stimulated (for 3 days) PBMC with anti-Ki-67 (Ki-67) Alexa Fluor 647.

Flow Cytometry (Intracellular) - Alexa Fluor® 488 Anti-Ki67 antibody [KI67] (AB206633)
  • Flow Cyt (Intra)

Supplier Data

Flow Cytometry (Intracellular) - Alexa Fluor® 488 Anti-Ki67 antibody [KI67] (AB206633)

Intracellular Flow Cytometry analysis of human peripheral blood mononuclear cells stimulated with PHA.Surface staining of CD25was followed by permeabilization and nuclear staining of Ki-67.

Immunocytochemistry - Alexa Fluor® 488 Anti-Ki67 antibody [KI67] (AB206633)
  • ICC

Supplier Data

Immunocytochemistry - Alexa Fluor® 488 Anti-Ki67 antibody [KI67] (AB206633)

Immunocytochemistry analysis of U2OS cells labelling Ki67 with ab206633 at 1 μg/mL. DAPI (blue) was used as a nuclear stain.

Key facts

Host species

Mouse

Clonality

Monoclonal

Clone number

KI67

Isotype

IgG1

Conjugation

Alexa Fluor® 488

Excitation/Emission

Ex: 495nm, Em: 519nm

Carrier free

No

Reacts with

Human

Applications

ICC, Flow Cyt (Intra)

applications

Immunogen

Cell preparation containing MKI67 protein. The exact immunogen used to generate this antibody is proprietary information.

P46013

Reactivity data

{ "title": "Reactivity Data", "filters": { "stats": ["", "Species", "Dilution Info", "Notes"], "tabs": { "all-applications": {"fullname" : "All Applications", "shortname": "All Applications"}, "ICC" : {"fullname" : "Immunocytochemistry", "shortname":"ICC"}, "FlowCytIntra" : {"fullname" : "Flow Cytometry (Intracellular)", "shortname":"Flow Cyt (Intra)"} }, "product-promise": { "all": "all", "testedAndGuaranteed": "tested", "guaranteed": "expected", "predicted": "predicted", "notRecommended": "not-recommended" } }, "values": { "Human": { "ICC-species-checked": "testedAndGuaranteed", "ICC-species-dilution-info": "1 µg/mL", "ICC-species-notes": "<p></p>", "FlowCytIntra-species-checked": "testedAndGuaranteed", "FlowCytIntra-species-dilution-info": "4 µL for 10^6 Cells", "FlowCytIntra-species-notes": "<p></p>" } } }

Product details

This antibody is designed for intracellular flow cytometric analysis of human blood cells using 4 μl reagent per 100 μl of whole blood, or 106 cells in a suspension. The contents of a vial (0.4 ml) is sufficient for 100 tests.

Properties and storage information

Form
Liquid
Purification technique
Size-exclusion chromatography
Storage buffer
pH: 7.4 Preservative: 0.0975% Sodium azide Constituents: PBS
Shipped at conditions
Blue Ice
Appropriate short-term storage conditions
+4°C
Appropriate long-term storage conditions
+4°C
Storage information
Store in the dark

Supplementary information

This supplementary information is collated from multiple sources and compiled automatically.

Ki67 is a nuclear protein often referred to as MKI67 with a molecular weight of approximately 345 kDa. This protein is strongly associated with cell proliferation. Scientists commonly use Ki67 staining techniques to identify and quantify proliferating cells in tissues. Ki67 is expressed in the nucleus during active cell cycle phases—G1 S G2 and M—but not in resting cells in G0 phase. It is detectable through methods such as Ki67 immunofluorescence and Ki67 flow cytometry which are important for analyzing cell division.
Biological function summary

The Ki67 protein plays an essential role in cellular proliferation processes. It does not form part of a stable complex but interacts transiently with other cell cycle-related proteins. Research indicates that Ki67 maintains the structure of the perichromosomal layer during mitosis impacting chromosome separation. It is particularly active in tissues with high cell turnover such as bone marrow and lymphoid organs.

Pathways

Ki67 influences several key cellular pathways that control cell proliferation and differentiation. The protein acts within the regulation of the cell cycle and the PI3K/AKT signaling pathway important for cell growth and survival. Within these pathways Ki67 interacts with proteins like cyclin-dependent kinases (CDKs) which regulate transitions between different phases of the cell cycle.

Ki67 has significant implications in oncology and can be used as a biomarker for cancer prognosis. Its expression levels help determine the aggressiveness of tumors especially in breast cancer and prostate cancer. High Ki67 levels correlate with poor prognosis as it indicates rapid cell division. In cancer Ki67 associates with p53 a protein that regulates the cell cycle and function as a tumor suppressor.

Product protocols

For this product, it's our understanding that no specific protocols are required. You can visit:

Target data

Protein that associates with the surface of mitotic chromosomes and acts both as a chromosome repellent during early mitosis and chromosome attractant during late mitosis (PubMed : 27362226, PubMed : 32879492, PubMed : 35513709, PubMed : 39153474). Required to maintain individual mitotic chromosomes dispersed in the cytoplasm following nuclear envelope disassembly (PubMed : 27362226). During early mitosis, relocalizes from nucleoli to the chromosome surface where it forms extended brush structures that cover a substantial fraction of the chromosome surface (PubMed : 27362226). The MKI67 brush structure prevents chromosomes from collapsing into a single chromatin mass by forming a steric and electrostatic charge barrier : the protein has a high net electrical charge and acts as a surfactant, dispersing chromosomes and enabling independent chromosome motility (PubMed : 27362226). During mitotic anaphase, the MKI67 brush structure collapses and MKI67 switches from a chromosome repellent to a chromosome attractant to promote chromosome clustering and facilitate the exclusion of large cytoplasmic particles from the future nuclear space (PubMed : 32879492, PubMed : 39153474). Mechanistically, dephosphorylation during mitotic exit and simultaneous exposure of a conserved basic patch induce the RNA-dependent formation of a liquid-like condensed phase on the chromosome surface, promoting coalescence of neighboring chromosome surfaces and clustering of chromosomes (PubMed : 39153474). Binds premature ribosomal RNAs during anaphase; promoting liquid-liquid phase separation (PubMed : 28935370, PubMed : 39153474). Binds DNA, with a preference for supercoiled DNA and AT-rich DNA (PubMed : 10878551). Does not contribute to the internal structure of mitotic chromosomes (By similarity). May play a role in chromatin organization; it is however unclear whether it plays a direct role in chromatin organization or whether it is an indirect consequence of its function in mitotic chromosome (PubMed : 24867636).
See full target information MKI67

Publications (7)

Recent publications for all applications. Explore the full list and refine your search

Cells 14: PubMed40643462

2025

Insulin Modulates NK Cell Activity in Liver Fibrosis MASH Patients via the STING Pathway.

Applications

Unspecified application

Species

Unspecified reactive species

Johnny Amer,Ahmad Salhab,Amiram Ariel,Rifaat Safadi

Gut pathogens 16:16 PubMed38521943

2024

Constituents of stable commensal microbiota imply diverse colonic epithelial cell reactivity in patients with ulcerative colitis.

Applications

Unspecified application

Species

Unspecified reactive species

Ruta Inciuraite,Rolandas Gedgaudas,Rokas Lukosevicius,Deimante Tilinde,Rima Ramonaite,Alexander Link,Neringa Kasetiene,Mindaugas Malakauskas,Gediminas Kiudelis,Laimas Virginijus Jonaitis,Juozas Kupcinskas,Simonas Juzenas,Jurgita Skieceviciene

Scientific reports 14:4456 PubMed38396014

2024

Prolonged culturing of colonic epithelial organoids derived from healthy individuals and ulcerative colitis patients results in the decrease of LINE-1 methylation level.

Applications

Unspecified application

Species

Unspecified reactive species

Ruta Inciuraite,Ruta Steponaitiene,Odeta Raudze,Ugne Kulokiene,Vytautas Kiudelis,Rokas Lukosevicius,Rasa Ugenskiene,Kestutis Adamonis,Gediminas Kiudelis,Laimas Virginijus Jonaitis,Juozas Kupcinskas,Jurgita Skieceviciene

EBioMedicine 91:104577 PubMed37068348

2023

Microwave hyperthermia represses human papillomavirus oncoprotein activity and induces cell death due to cell stress in 3D tissue models of anogenital precancers and cancers.

Applications

Unspecified application

Species

Unspecified reactive species

Michaela J Conley,Ilaria Epifano,Anna Kirk,Andrew Stevenson,Sheila V Graham

International journal of molecular sciences 24: PubMed36614145

2022

E3 Ubiquitin Ligase Midline 1 Regulates Endothelial Cell ICAM-1 Expression and Neutrophil Adhesion in Abdominal Sepsis.

Applications

Unspecified application

Species

Unspecified reactive species

Feifei Du,Avin Hawez,Zhiyi Ding,Yongzhi Wang,Carl-Fredrik Rönnow,Milladur Rahman,Henrik Thorlacius

Acta pharmacologica Sinica 43:1843-1856 PubMed34845369

2021

Ras inhibitor farnesylthiosalicylic acid conjugated with IR783 dye exhibits improved tumor-targeting and altered anti-breast cancer mechanisms in mice.

Applications

Unspecified application

Species

Unspecified reactive species

Qiu-Ju Huang,Guo-Chao Liao,Xue-Rong Zhuang,Meng-Lan Yang,Jing-Jing Yao,Jian-Hua Deng,Yan-Min Zhang,Ying Wang,Xiao-Xiao Qi,Dong-Feng Pan,Yang Guan,Zhi-Ying Huang,Feng-Xue Zhang,Zhong-Qiu Liu,Lin-Lin Lu

Oncology letters 22:637 PubMed34295384

2021

Targeting FHL2-E-cadherin axis by miR-340-5p attenuates colon cancer cell migration and invasion.

Applications

Unspecified application

Species

Unspecified reactive species

Anwar Algaber,Raed Madhi,Avin Hawez,Carl-Fredrik Rönnow,Milladur Rahman
View all publications

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