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anti-Mouse (Murine) KI-67 Antibodies:
anti-Human KI-67 Antibodies:
anti-Rat (Rattus) KI-67 Antibodies:
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Human Polyclonal KI-67 Primary Antibody for WB - ABIN3042997
Liu, Zhou, Wang, Geng, Liu: Roux-en-Y gastric bypass-induced improvement of glucose tolerance and insulin resistance in type 2 diabetic rats are mediated by glucagon-like peptide-1. in Obesity surgery 2011
Show all 30 Pubmed References
Human Polyclonal KI-67 Primary Antibody for ICC, IHC (p) - ABIN3044570
Shan, Li, Newton, Zhao, Li, Guo: A novel protein extracted from foxtail millet bran displays anti-carcinogenic effects in human colon cancer cells. in Toxicology letters 2014
Show all 30 Pubmed References
Human Monoclonal KI-67 Primary Antibody for IHC (p) - ABIN1687925
Mellick, Plummer, Nolan, Gao, Bambino, Hahn, Catena, Turner, McDonnell, Benezra, Brink, Swarbrick, Mittal: Using the transcription factor inhibitor of DNA binding 1 to selectively target endothelial progenitor cells offers novel strategies to inhibit tumor angiogenesis and growth. in Cancer research 2010
Show all 379 Pubmed References
Human Monoclonal KI-67 Primary Antibody for IHC (p) - ABIN1687135
Sanmamed, Rodriguez, Schalper, Oñate, Azpilikueta, Rodriguez-Ruiz, Morales-Kastresana, Labiano, Pérez-Gracia, Martín-Algarra, Alfaro, Mazzolini, Sarno, Hidalgo, Korman, Jure-Kunkel, Melero: Nivolumab and Urelumab Enhance Antitumor Activity of Human T Lymphocytes Engrafted in Rag2-/-IL2Rγnull Immunodeficient Mice. in Cancer research 2015
Show all 406 Pubmed References
Dog (Canine) Monoclonal KI-67 Primary Antibody for ICC, IHC (fro) - ABIN269440
Koya, Lu, Sun, Purich, Atkinson, Li, Yang et al.: Reversal of streptozotocin-induced diabetes in mice by cellular transduction with recombinant pancreatic transcription factor pancreatic duodenal homeobox-1: a novel protein transduction domain-based ... in Diabetes 2008
Show all 28 Pubmed References
Human Polyclonal KI-67 Primary Antibody for ICC, IHC (fro) - ABIN152984
Gerdes, Li, Schlueter, Duchrow, Wohlenberg, Gerlach, Stahmer, Kloth, Brandt, Flad: Immunobiochemical and molecular biologic characterization of the cell proliferation-associated nuclear antigen that is defined by monoclonal antibody Ki-67. in The American journal of pathology 1991
Show all 58 Pubmed References
Human Polyclonal KI-67 Primary Antibody for ICC, FACS - ABIN409932
Baek, Pishvaian, Tang, Kim, Yang, Zouhairi, Mendelson, Shetty, Kallakury, Berry, Shin, Mishra, Reddy, Kim, Mishra: Transforming growth factor-β adaptor, β2-spectrin, modulates cyclin dependent kinase 4 to reduce development of hepatocellular cancer. in Hepatology (Baltimore, Md.) 2011
Show all 31 Pubmed References
Human Polyclonal KI-67 Primary Antibody for IF (cc), IF (p) - ABIN677858
Kim, Lim, Kim, Kim, Kim, Tian, Park, Park, Choung: The oncoprotein, gankyrin, is up-regulated in middle ear cholesteatoma. in Acta oto-laryngologica 2014
Show all 16 Pubmed References
Human Polyclonal KI-67 Primary Antibody for FACS, ICC - ABIN409934
Mobley, Bryant, Richard, Brann, Firestein, Greer: Age-dependent regional changes in the rostral migratory stream. in Neurobiology of aging 2013
Show all 12 Pubmed References
Human Polyclonal KI-67 Primary Antibody for ICC, IF - ABIN409940
Fung, Jonkman, Tannock et al.: Quantitative immunohistochemistry for evaluating the distribution of Ki67 and other biomarkers in tumor sections and use of the method to study repopulation in xenografts after treatment with ... in Neoplasia (New York, N.Y.) 2012
Show all 8 Pubmed References
After intrastromal scanning of cornea, expression of Ki-67 increases.
injection of a b3-adrenergic receptor (b3-AR) agonist for continuous 5 days increased the number of Ki67-positive brown adipocytes even at Day 1 but not that of SV cells. In addition, the b3-AR antagonist, but not b1-AR antagonist, attenuated the cold exposure-induced increase in the number of Ki67-positive brown adipocytes
Ki67-positive cells are localized near inner enamel epithelium and supra-IEE, the stellate reticulum next to these is Ki67-negative. The IEE and supra-IEE contain intense Ki67-immunoreactivity, outer enamel epithelium lacks proliferative cells in mice.
Whey proteins reduced Ki-67 and 8-OHdG expression in the skin of chronically UVB-irradiated mice.
Both HDAC1 (show HDAC1 Antibodies) and HDAC2 (show HDAC2 Antibodies) play crucial roles in the regulation of liver regeneration. The loss of HDAC1 (show HDAC1 Antibodies)/2 inhibits Ki67 expression and results in defective hepatocyte mitosis and impaired liver regeneration.
Intratumoral FLT uptake level markedly decreased at 6 h and then gradually increased with time.
Late stage cathepsin C (show CTSC Antibodies), CXCL13 (show CXCL13 Antibodies) and Ki-67 overexpression correlate with regional neuropathology in a bovine spongiform encephalopathy transgenic murine model.
The majority of tumours showed strong p16 (show CDKN2A Antibodies), p21 (show D4S234E Antibodies), p27 (show CDKN1B Antibodies), pRb (show PGR Antibodies) and cyclin D1 (show CCND1 Antibodies) staining and little or no p53 (show TP53 Antibodies) expression. Tumours harbouring dysplasia were significantly more likely to be p53 (show TP53 Antibodies)-positive and exhibit up-regulated p21 (show D4S234E Antibodies) and p27 (show CDKN1B Antibodies).
Vascular endothelial growth factor (VEGF) expression correlates with p53 and ki-67 expressions in tongue squamous cell carcinoma.
Age-related changes in proliferative markers in labial (show LAT2 Antibodies) salivary glands: a study of argyrophilic nucleolar organizer regions (AgNORs) and Ki-67
p63 (show CKAP4 Antibodies) protein is essential for the embryonic development of vibrissae and teeth; while it localizes with K5 in vibrissae, it is not fully colocalized with nuclear Ki67 expression
Here the authors show how Ki-67 and RepoMan form mitotic exit phosphatases by recruiting PP1 (show PPA1 Antibodies), how they distinguish between distinct PP1 (show PPA1 Antibodies) isoforms and how the assembly of these two holoenzymes are dynamically regulated by Aurora B kinase (show AURKB Antibodies) during mitosis.
Ki-67 before and after NAC (show NLRP1 Antibodies), as well as the change of Ki-67 before and after NAC (show NLRP1 Antibodies) might be prognostic factors for OS and DFS (show FST Antibodies) for breast cancer patients.
Ki67 depletion results in the dissociation of both pre-ribosomal RNAs and nucleolar proteins from the perichromosomal layer (PCL (show PKD2L1 Antibodies)), which indicates that Ki67 is required for the PCL (show PKD2L1 Antibodies) accumulation of pre-ribosomal RNAs, to which several nucleolar proteins are associated.
Variants near TTN (show TTN Antibodies) and CCDC8 (show CCDC8 Antibodies) were associated with KI67 expression, and rs2288563 and rs2562832 in TTN (show TTN Antibodies) are potential biomarkers for the prediction of clinical outcomes in hepatitis B-related hepatocellular carcinoma patients.
suggest that upregulation of NG2/CSPG4 (show MCSP Antibodies) rather than changes in CD44 (show CD44 Antibodies) or Ki-67 expression is associated with low overall survival in glioblastoma multiforme patients, supporting NG2/CSPG4 (show MCSP Antibodies) as a potential prognostic marker in glioblastoma
There are considerable differences between the different Ki-67 antibodies in their capacity to detect proliferating tumor cells and to separate low- and high-risk breast cancer patient groups.
Study shows that a Ki67 increase occurs in a significant proportion of patients with entero-pancreatic neuroendocrine neoplasms at time of disease progression, particularly in those with pancreatic origin.
Anillin (ANLN (show ANLN Antibodies)) expression in tumor cells is correlated to poor prognosis in breast cancer patients, independent of Ki-67 or tumor size.
Differences in Ki67 expressions between pre- and post-neoadjuvant chemotherapy specimens might predict early recurrence of breast cancer.
Neoadjuvant therapy in microsatellite-stable colorectal carcinoma induces concomitant loss of MSH6 (show MSH6 Antibodies) and Ki-67 expression.
This gene encodes a nuclear protein that is associated with and may be necessary for cellular proliferation. Alternatively spliced transcript variants have been described. A related pseudogene exists on chromosome X.
antigen identified by monoclonal antibody Ki-67
, antigen KI-67-like
, antigen KI-67
, proliferation-related Ki-67 antigen