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腫瘤蛋白p53(P53)活性蛋白

Active Tumor Protein p53 (P53)

TP53; LFS1; TRP53; Li-Fraumeni Syndrome; Cellular tumor antigen p53; Antigen NY-CO-13; Phosphoprotein p53; Tumor suppressor p53

  • 腫瘤蛋白p53(P53)活性蛋白產品包裝(模擬)
  • 腫瘤蛋白p53(P53)活性蛋白產品包裝(模擬)
  • 腫瘤蛋白p53(P53)活性蛋白Figure. Gene Sequencing (Extract)
  • APA928Hu01.pngFigure. SDS-PAGE
  • 腫瘤蛋白p53(P53)活性蛋白Figure. Western Blot
  • Certificate通過ISO 9001、ISO 13485質量體系認證

活性實驗

Figure. Inhibition of Jurkat cell proliferation after stimulated with TP53
Tumor protein p53, also known as p53, cellular tumor antigen p53 (UniProt name), phosphoprotein p53, tumor suppressor p53, antigen NY-CO-13, or transformation- related protein 53 (TRP53), is any isoform of a protein encoded by homologous genes in various organisms, such as TP53 (humans) and Trp53 (mice). TP53 involved in cell cycle regulation as a trans-activator that acts to negatively regulate cell division by controlling a set of genes required for this process. One of the activated genes is an inhibitor of cyclin-dependent kinases. To test the effect of TP53 on cell apoptosis, Jurkat cells were seeded into triplicate wells of 96-well plates at a density of 5,000 cells/well with 1% serum standard 1640 including various concentrations of recombinant human TP53. After incubated for 72h,?cells were observed by inverted microscope and cell proliferation was measured by Cell Counting Kit-8 (CCK-8). Briefly, 10μL of CCK-8 solution was added to each well of the plate, then the absorbance at 450nm was measured using a microplate reader after incubating the plate for 1-4 hours at 37℃. Proliferation of Jurkat cells after incubation with TP53 for 72h observed by inverted microscope was shown in Figure 1. Cell viability was assessed by CCK-8 (Cell Counting Kit-8) assay after incubation with recombinant TP53 for 72h. The result was shown in Figure 2. It was obvious that TP53 significantly inhibit cell viability of Jurkat cells.
(A) Jurkat cells cultured in 1640, stimulated with 1ug/mL TP53 for 72h;
(B) Unstimulated Jurkat cells cultured in 1640 for 72h.

Figure. Inhibition of Jurkat cell proliferation after stimulated with TP53.

用法

Reconstitute in ddH2O to a concentration of 0.1-1.0 mg/mL. Do not vortex.

儲存

避免反復凍融。2-8°C不超過一個月,-80°C不超過12個月。

穩(wěn)定性

熱穩(wěn)定性以損失率顯示。損失率是由加速降解試驗決定,具體方法如下:在37°C孵育48小時,沒有顯著的降解或者沉淀產生。保質期內,在適當的條件下存儲,損失率低于5%。

相關產品

編號適用物種:Homo sapiens (Human,人)應用(僅供研究使用,不用于臨床診斷!)
RPA928Hu01腫瘤蛋白p53(P53)重組蛋白Positive Control; Immunogen; SDS-PAGE; WB.
RPA928Hu02腫瘤蛋白p53(P53)重組蛋白Positive Control; Immunogen; SDS-PAGE; WB.
RPA928Hu03腫瘤蛋白p53(P53)重組蛋白Positive Control; Immunogen; SDS-PAGE; WB.
APA928Hu01腫瘤蛋白p53(P53)活性蛋白Cell?culture;?Activity?Assays.
PAA928Hu01腫瘤蛋白p53(P53)多克隆抗體WB; IHC; ICC/IF
PAA928Hu02腫瘤蛋白p53(P53)多克隆抗體WB; IHC; FCM
LAA928Hu71腫瘤蛋白p53(P53)多克隆抗體(生物素標記)WB; IHC; ICC.
MAA928Hu22腫瘤蛋白p53(P53)單克隆抗體WB
MAA928Hu24腫瘤蛋白p53(P53)單克隆抗體WB; IHC; ICC; IP.
MAA928Hu25腫瘤蛋白p53(P53)單克隆抗體WB
MAA928Hu27腫瘤蛋白p53(P53)單克隆抗體WB
MAA928Hu21腫瘤蛋白p53(P53)單克隆抗體WB
MAA928Hu23腫瘤蛋白p53(P53)單克隆抗體WB
FAA928Hu04抗腫瘤蛋白p53(P53)單克隆抗體FCM
FAA928Hu02抗腫瘤蛋白p53(P53)單克隆抗體FCM
SEA928Hu腫瘤蛋白p53(P53)檢測試劑盒(酶聯免疫吸附試驗法)Enzyme-linked immunosorbent assay for Antigen Detection.
SCA928Hu腫瘤蛋白p53(P53)檢測試劑盒(化學發(fā)光免疫分析法)Chemiluminescent immunoassay for Antigen Detection.
LMA928Hu腫瘤蛋白p53(P53)等多因子檢測試劑盒(流式熒光發(fā)光法)FLIA Kit for Antigen Detection.
KSA928Hu01腫瘤蛋白p53(P53)檢測試劑盒DIY材料(酶聯免疫吸附試驗法)Main materials for "Do It (ELISA Kit) Yourself".

參考文獻

雜志參考文獻
Anticancer ResearchAnalysis of p53 and miRNA expression after irradiation of glioblastoma cell lines[PubMed: 23155233]
Microscopy Research and TechniqueTherapeutic role of curcumin in oxidative DNA damage caused by formaldehyde[PubMed: 25761397]
J Nutr BiochemSupplementation with Selenium yeast on the prooxidant–antioxidant activities and anti-tumor effects in breast tumor xenograft-bearing mice[PubMed: 26344777]
Biochemical and Biophysical Research CommunicationsTranscription factor HBP1: A regulator of senescence and apoptosis of preadipocytes[Pubmed: 31331641]
Folia BiologicaEffect of Graviola (Annona Muricata l.) and Ginger (Zingiber Officinale Roscoe) on Diabetes Mellitus Induced in Male Wistar Albino Rats[]
Non-POU Domain-Containing Octamer-Binding (NONO) Protein Stability Regulated by PIN1 is Crucial for Breast Cancer Tumorigenicity Via the MAPK/β?…[]