Cdc25C (G210) pAb host: Rabbit
- Known as:
- Cdc25C (G210) pAb production species: Rabbit
- Catalog number:
- bs1047
- Product Quantity:
- USD
- Category:
- -
- Supplier:
- Bioworld
- Gene target:
- Cdc25C (G210) pAb host: Rabbit
Related genes to: Cdc25C (G210) pAb host: Rabbit
- Gene:
- CDC25C NIH gene
- Name:
- cell division cycle 25C
- Previous symbol:
- CDC25
- Synonyms:
- PPP1R60
- Chromosome:
- 5q31.2
- Locus Type:
- gene with protein product
- Date approved:
- 1992-02-06
- Date modifiied:
- 2017-12-06
- Gene:
- PPP1R18 NIH gene
- Name:
- protein phosphatase 1 regulatory subunit 18
- Previous symbol:
- KIAA1949
- Synonyms:
- phostensin
- Chromosome:
- 6p21.33
- Locus Type:
- gene with protein product
- Date approved:
- 2004-03-02
- Date modifiied:
- 2016-10-05
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guanine nucleotide binding protein alpha inhibiting activity polypeptide 1 (GNAI1) polyclonal antibody kinase suppressor of ras (KSR) polyclonal antibody'F 4_80 Antigen (mouse) Host Rat'F 4_80 Antigen (mouse) Host Rat(Alpha)_ 1 _ antitrypsin (A1AT) POLYCLONAL Rabbit anti_human(Alpha)_ Feto Protein (AFP) POLYCLONAL Rabbit anti_human(Alpha)_ Feto Protein (AFP) POLYCLONAL Rabbit anti_human(Alpha)_1_ antitrypsin (A1AT) POLYCLONAL Rabbit anti_human(Arg6,b_cyclohexyl_Ala8,D_Tic16,Arg17,Cys18)_Atrial Natriuretic Factor (6_18) amide (mouse, rabbit, rat) Salt _ Binding (Disulfide_bond) Synonym A71915 SumFormula C69H116N26O15S2(Arg6,b_cyclohexyl_Ala8,D_Tic16,Arg17,Cys18)_Atrial Natriuretic Factor (6_18) amide (mouse, rabbit, rat) Salt _ Binding (Disulfide_bond) Synonym A71915 SumFormula C69H116N26O15S2(Arg6,β-cyclohexyl-Ala8,D-Tic16,Arg17,Cys18)-Atrial Natriuretic Factor (6-18) amide (mouse, rabbit, rat)
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- Studies have shown that PANoptosis is increasingly involved in cancer and cancer treatment. The Cordycepin has also been found to be involved in the development of various cancers. However, relevant research on both in lung adenocarcinoma (LUAD) remains relatively scarce. The present study aims to identify potential prognostic genes in LUAD and elucidate their impact on the prognosis of LUAD patients, with the goal of providing novel insights into the therapeutic strategies for this disease. - Source: PubMed
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Xu HaoranHuang WenhuiYang QingChen YueweiSu PeiyuanFu Bing - Oral squamous cell carcinoma (OSCC) remains a substantial global health burden. According to the latest global cancer statistics, it accounts for an estimated 300,000 new cases and 100,000 deaths annually. This study aimed to investigate the pharmacological effects of digitoxin, a cardenolide glycoside, on the modulation of proliferative capacity and apoptotic induction in human OSCC human tongue squamous carcinoma (HSC-3) cells. - Source: PubMed
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Tang WenruiWang LinYan XudongZhang JishengYu LonggangChen HanZheng ChungeDong ZihuiZheng QianyouHan LinJiang Yan - Polyethylene terephthalate (PET), one of the most widely used synthetic polymers globally, has emerged as a potential environmental risk factor for human health. However, the molecular mechanisms linking PET exposure to hepatocellular carcinoma (HCC) remain poorly understood. - Source: PubMed
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Chen PengLiu XinYuan DongmeiZheng LanDu YuminGong DacaiWei XingWang DanXu GeGe Bin - Subsequently to the publication of the above article, a concerned reader drew to the Editor's attention that the β‑actin bands featured in Fig. 1A were also apparently included in the 'Ctrl' experiments for the phospho‑P53 protein bands in Fig. 1B. In addition, a specific pair of P53 bands in Fig. 1B had also apparently been re‑used as phospho‑CDC25C bands in Fig. 6A, suggesting that these figures may have potentially undergone inappropriate editing. After having evaluated these data independently in the Editorial Office, the concerns of the reader were shown to have been well‑founded. Therefore, in view of the uncertainties regarding the assembly of some of the western blot data in Figs. 1 and 6, the Editor of has decided that this paper should be retracted from the Journal on account of uncertainties with the presentation of the abovementioned data. The authors were asked for an explanation to account for these concerns, but the Editorial Office did not receive a reply.The Editor apologizes to the readership for any inconvenience caused. [Oncology Reports 35: 2707‑2714, 2016; DOI: 10.3892/or.2016.4674]. - Source: PubMed
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