生物源
mouse
共軛
unconjugated
抗體表格
ascites fluid
無性繁殖
DCS-22, monoclonal
分子量
antigen 31-34 kDa
包含
15 mM sodium azide
物種活性
canine, human, rat, monkey, mouse
技術
immunocytochemistry: suitable
immunohistochemistry (formalin-fixed, paraffin-embedded sections): suitable
immunoprecipitation (IP): suitable
indirect ELISA: suitable
microarray: suitable
western blot: 1:4,000 using a rat osteosarcoma cell line (ROS) extract
同型
IgG1
運輸包裝
dry ice
儲存溫度
−20°C
基因資訊
human ... CCND3(896)
mouse ... Ccnd3(12445)
rat ... Ccnd3(25193)
特異性
It does not cross-react with other D-type cyclins.
免疫原
recombinant human cyclin D3 protein.
International journal of cancer, 65(3), 323-327 (1996-01-26)
The D-type cyclins are positive regulators of the G1 phase of the mammalian cell cycle. Cyclins D1 or D2 are over-expressed in several types of cancer, transform rodent cells in culture and therefore harbor hallmarks of cellular proto-oncogenes. In contrast
Journal of virology, 80(11), 5577-5587 (2006-05-16)
In its course of human infection, varicella-zoster virus (VZV) infects rarely dividing cells such as dermal fibroblasts, differentiated keratinocytes, mature T cells, and neurons, none of which are actively synthesizing DNA; however, VZV is able to productively infect them and
Toxicology letters, 155(1), 73-85 (2004-12-09)
The influence of single-walled carbon nanotubes (SWCNTs) on human HEK293 cells is investigated with the aim of exploring SWCNTs biocompatibility. Results showed that SWCNTs can inhibit HEK293 cell proliferation, decrease cell adhesive ability in a dose- and time-dependent manner. HEK293
Proceedings of the National Academy of Sciences of the United States of America, 102(34), 12129-12134 (2005-08-16)
Rhabdoid tumors are aggressive pediatric malignancies for which, currently, there are no effective or standard treatment strategies. Rhabdoid tumors arise because of the loss of the tumor suppressor gene INI1. We have previously demonstrated that INI1 represses Cyclin D1 transcription
Glia, 57(2), 222-233 (2008-08-30)
In previous studies, we showed that endothelin-1 increased astrocyte proliferation and glucose uptake. These effects were similar to those observed with other gap junction inhibitors, such as carbenoxolone (CBX). Because 24-h treatment with endothelin-1 or CBX downregulates the expression of
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