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Human KI-67 ELISA Kit for Sandwich ELISA - ABIN832326
Chiu, Nakano, Chen, Hsu, Lai, Huang, Cheng, Goto, Chen: Repeated-measures implication of hepatocellular carcinoma biomarkers in living donor liver transplantation. in PLoS ONE 2015
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 ELISA Kits) and HDAC2 (show HDAC2 ELISA Kits) play crucial roles in the regulation of liver regeneration. The loss of HDAC1 (show HDAC1 ELISA Kits)/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 ELISA Kits), CXCL13 (show CXCL13 ELISA Kits) and Ki-67 overexpression correlate with regional neuropathology in a bovine spongiform encephalopathy transgenic murine model.
The majority of tumours showed strong p16, p21, p27 (show CDKN1B ELISA Kits), pRb (show PGR ELISA Kits) and cyclin D1 (show CCND1 ELISA Kits) staining and little or no p53 (show TP53 ELISA Kits) expression. Tumours harbouring dysplasia were significantly more likely to be p53 (show TP53 ELISA Kits)-positive and exhibit up-regulated p21 and p27 (show CDKN1B ELISA Kits).
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 ELISA Kits) salivary glands: a study of argyrophilic nucleolar organizer regions (AgNORs) and Ki-67
p63 (show CKAP4 ELISA Kits) 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
The results demonstrate that high expression of Ki-67 contributes to radiation resistance and acts a poor prognosis indicator in patients with locally advanced nasopharyngeal carcinoma.
Here the authors show how Ki-67 and RepoMan form mitotic exit phosphatases by recruiting PP1 (show PPA1 ELISA Kits), how they distinguish between distinct PP1 (show PPA1 ELISA Kits) isoforms and how the assembly of these two holoenzymes are dynamically regulated by Aurora B kinase (show AURKB ELISA Kits) during mitosis.
Ki-67 before and after NAC (show NLRP1 ELISA Kits), as well as the change of Ki-67 before and after NAC (show NLRP1 ELISA Kits) might be prognostic factors for OS and DFS (show FST ELISA Kits) for breast cancer patients.
Ki67 depletion results in the dissociation of both pre-ribosomal RNAs and nucleolar proteins from the perichromosomal layer (PCL), which indicates that Ki67 is required for the PCL accumulation of pre-ribosomal RNAs, to which several nucleolar proteins are associated.
Variants near TTN (show TTN ELISA Kits) and CCDC8 (show CCDC8 ELISA Kits) were associated with KI67 expression, and rs2288563 and rs2562832 in TTN (show TTN ELISA Kits) are potential biomarkers for the prediction of clinical outcomes in hepatitis B-related hepatocellular carcinoma patients.
suggest that upregulation of NG2/CSPG4 (show MCSP ELISA Kits) rather than changes in CD44 (show CD44 ELISA Kits) or Ki-67 expression is associated with low overall survival in glioblastoma multiforme patients, supporting NG2/CSPG4 (show MCSP ELISA Kits) 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 ELISA Kits)) 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.
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