This is a Validated Antibody Database (VAD) review about BrdU/bromodeoxyuridine, based on 74 published articles (read how Labome selects the articles), using BrdU/bromodeoxyuridine product in experiments. It is aimed to help Labome visitors find the most suited BrdU/bromodeoxyuridine. Please note the number of articles fluctuates since newly identified citations are added and citations for discontinued catalog numbers are removed regularly.
synonym: nonradioactive BrdU–based cell proliferation assay, BrdU labeling reagent, BrdU, BrdU-labelling reagent, BrdU detection kit, Bromodeoxyuridine labeling reagent, FITC BrdU Flow Kit, kit for bromodeoxyuridine (BrdU) incorporation assays, colorimetric 5-bromo-2-deoxyuridine (BrdU) Cell Proliferation ELISA Kit, BrdU labeling and detection kit I, BrdU-labeling assay kit, bromodeoxyuridine, BrdU Immunohistochemistry System, BrdU-POD

Roche BrdU was used to perform cell labeling in order to study the role of Hedgehog signaling pathway in neuroblast proliferation and neurogenesis to the paper
Roche Applied Sciences BrdU was used in 20 mg/ml to perform BrdU labeling in order to show that mammals may have cardiac regeneration ability for a brief period after birth to the paper
Roche anti-BrdU-POD antibody was used to perform immunohistochemistry in order to show that beta 1 integrin-mediated adhesion signalling plays an important role in epidermal progenitor cell expansion to the paper
Roche mouse monoclonal anti-BrdU antibody was used to perform immunohistochemistry in order to show that the I268N mutation in Egr2 can lead to abnormal peripheral nerve myelination to the paper
Roche BrdU-labeling assay kit was used for cell BrdU incorporation in order to study the effect of the interaction of CRTC1 with AP-1 on cell proliferation and transformation to the paper
Roche bromodeoxyuridine was used to treat the cells in order to study the function of beta-catenin in mediating the effects of ionizing radiation in fibroblasts to the paper
Roche Applied Science kit for bromodeoxyuridine (BrdU) incorporation assays were used to assess DNA synthesis in order to study the role for gamma-aminobutyric acid in suppressing small airway-derived lung adenocarcinoma in sections from hamster lung tissues to the paper
Abcam anti-BrdU antibody was used in immunohistochemistry in order to demonstrate that BIM is required for caspase-dependent cell death in the mammary gland and that in the absence of primary death mechanisms, such as apoptosis, alternative clearance mechanisms contribute to proper lumen formation in the mammary gland in vivo Ab6326to the paper
Abcam rat monoclonal anti-BrdU was used in 1:200 to perform immunocytochemistry in order to show that obesity in db/db mice could be rescued by hypothalamic neuron transplantation to the paper
Abcam rat monoclonal anti-BrdU was used in 1:25 to perform immunohistochemistry in order to show that mammals may have cardiac regeneration ability for a brief period after birth to the paper
Abcam rat polyclonal anti-BrdU was used to perform immunohistochemistry in order to show that Agouti expression could be affected by environment resulting in color pattern evolution to the paper
Abcam Inc BrdU antibody was used to perform immunohistochemistry in order to investigate the relations between cholecystokinin-2 receptor and colorectal cancer to the paper
Abcam anti-alpha-BrdU antibody was used to perform ChIP assays in order to study the regulation effect of cyclin A-cdk1 to the paper
Abcam BrdU antibody was used for immunohistochemistry in order to investigate the effect of merlin on glial cell growth to the paper
Abcam rat anti-BrdU antibody was used to perform immunocytochemistry in order to study the contribution of hSRBC epigenetic inactivation to the malignant progression in gastric cancer through attenuated p53 response to stresses to the paper
Abcam rat anti-BrdU antibody was used in immunohistochemistry to study a role for Lhx2 in maintaining the growth and undifferentiated properties of hair follicle progenitors to the paper
Invitrogen BrdU labeling reagent was used in immunocytochemistry in order to study the role of trefoil factor 3 (TFF3) in beta-cell replication to the paper
AbD Serotec anti-BrdU antibody was used to perform western blot in order to study synaptic plasticity to the paper
AbD Serotec rat monoclonal anti-BrdU was used at 1:300 to perform immunohistochemistry in order to show that mammalian cerebral cortex contains fate-restricted neural progenitors to the paper
Oxford Biotech anti-BrdU was used in 1:100 dilution to perform immunohistochemistry in order to show that clonogenic neoblasts can be used for planarian regeneration to the paper
Serotec Rat anti-BrdU antibody was used to carry out immunofluorescence assays in order to determine the nature for epithelial defects in cornea of mice with a destrin deletion to the paper
Novus Biologicals rat anti-BrdU was used to perform immunohistochemistry in order to show that CNS synaptogenesis and repair were regulated by region-restricted astrocyte allocation to the paper
Sigma mouse monoclonal anti-BrdU was used in 1:50 to perform immunohistochemistry in order to show that proper organogenesis needs B-type lamins in mice B2531to the paper
Sigma BrdU was used to perform drug treatment in order to study the function of NDE1 in S phase of early neural progenitor differentiation to the paper
Sigma BrdU was used to perform cell labeling in order to investigate the roles of Vav2 and Vav3 in skin cancer to the paper
Sigma BrdU was used to perform flow cytometry in order to investigate the importance of TCR signaling to natural killer T cell development to the paper
Sigma mouse anti-BrdU antibody was used to perform immunohistochemistry in order to study the role of Hedgehog signaling pathway in neuroblast proliferation and neurogenesis to the paper
Sigma Aldrich BrdU was used to perform flow cytometry in orde to investigate the importance of phosphatase activity in B cell selection in germinal centers to the paper
Sigma-Aldrich BrdU was used to perform cell cycle analysis in order to investigate the regulatory effect of PD-1 on IgA selection and the composition of the gut microflora to the paper
Sigma-Aldrich BrdU was used in 100 mg/kg to perform BrdU staining in order to show that obesity in db/db mice could be rescued by hypothalamic neuron transplantation to the paper
Sigma BrdU was used in 0.5 mg/ml to perform BrdU immunostaining in order to show that Drosophila stem cell proliferation could be promoted by Wolbachia to the paper
Fluka BrdU was in 5 mg/mL used to perform immunohistochemistry in order to show that clonogenic neoblasts can be used for planarian regeneration to the paper
Sigma-Aldrich anti-BrdU antibody was used in immunohistochemistry in order to investigate the mechanism of how the unfolded protein response (UPR) promotes hypoxic tumor cells survival through autophagy to the paper
Sigma BrdU was used in BrdU incorporation assays in order to investigate the influence of gankyrin protein on p53 and Mdm2 to the paper
Sigma BrdU was used to assess cell proliferation in order to study the important role Ngn2 and NeuroD1 play in controlling neuronal commitment and hippocampal granule neuroblast formation to the paper
Sigma BrdU was used to label replication tracks in order to study the different mechanisms of the effect of Claspin and Chk1 on replication fork stability to the paper
Sigma-Aldrich BrdU was used to culture cells in DNA damage induction in order to study the role of MERIT40 in controlling BRCA1 Rap80 complex integrity and recruitment to DNA double-strand breaks to the paper
Sigma BrdU was used to perform labeling in order to study the function of C/EBP beta transactivated by p57Kip2 in changing chondrocytes from proliferation to hypertrophic differentiation to the paper
Sigma mouse anti-BrdU was used to perform immunohistochemistry in order to illustrate that the Bmi1 functions on neurons oxidative metabolism are associated with repression of p53 pro-oxidant activity to the paper
Sigma-Aldrich BrdU was used to inject to pregnant mice in order to demonstrate that embryonic lethality can be caused by mitochondrial degeneration rather than apoptosis in ceramide transfer protein mutant mice to the paper
Sigma 5-bromo-2-deoxyuridine (BrdU) was used for immunohistochemistry in order to investigate the effect of merlin on glial cell growth to the paper
Sigma primary antibody to BrdU was used to perform immunohistochemistry in order to study whether genetic manipulation of periostin expression in the heart affect myocyte content, cell cycle activity or cardiac repair to the paper
Sigma Chemical BrdU was used to label siRNA-treated keratinocytes in order to study the role for RhoE in keratinocyte differentiation and stratification to the paper
Sigma Bromodeoxyuridine labeling reagent was used in immunocytochemistry in order to investigate the regulatory role of transforming growth factor-beta in valve interstitial cell function during wound repair to the paper
Sigma BrdU was used to treat pregnant females mice in order to examine the consequences of over-expression of Pax6 for the eye and its axonal connections to the paper
Sigma-Aldrich BrdU was used to treat rats in order to study the effect of capsaicin on the nodose ganglia of adult rats to the paper
Sigma BrdU (50 uM) were used in proliferation analysis in order to gain insights into the molecular program that maintains DP cell fate to the paper
Sigma BrdU (5-bromo-2-deoxyuridine) was used to administer to mice in order to study the effect of antidepressant sertraline on the phenotype, neurogenesis, and BDNF levels in the R6/2 Huntington s disease mouse model to the paper
GE Healthcare Life Biosciences
Amersham anti-BrdU antibody was used in immunohistochemistry in order to demonstrate that BIM is required for caspase-dependent cell death in the mammary gland and that in the absence of primary death mechanisms, such as apoptosis, alternative clearance mechanisms contribute to proper lumen formation in the mammary gland in vivo RPN 202to the paper
Amersham mouse anti-BrdU was used in 1:100 to perform immunohistochemistry in order to show that Drosophila stem cell proliferation could be promoted by Wolbachia to the paper
Amersham BrdU-labelling reagent was used in cell proliferation assays in order to study the role of adhesion molecule nectin-1 in the regulation of desmosome assembly in mice to the paper
Accurate rat monoclonal anti-BrdU was used in 1:200 to perform immunohistochemistry in order to show that interneurons from the same progenitor cells could assemble together in the neocortex to the paper
Accurate rat anti-BrdU was used in 1:200 to perform immunohistochemistry in order to show that scars formed after spinal cord injury are derived from pericytes to the paper
Accurate Chemical anti-BrdU antibody was used to perform immunohistochemistry in order to study the roles of Atoh1 in sonic hedgehog signaling during the development of cerebellum to the paper
Promega BrdU (Accurate; diluted 1:1,000) was used in immunostaining in order to show that miR-9 suppresses TLX expression to negatively regulate neural stem cell proliferation and accelerate neural differentiation to the paper
Dako polyclonal anti-BrdU antibody was used in immunocytochemistry in order to investigate the influence of gankyrin protein on p53 and Mdm2 to the paper
DAKO BrdU antibody was used in immunohistochemistry to study the role of notch signaling in hair cell increases and cell differentiation in COUP-TFI-/- mice to the paper
BD Europe anti-BrdU was used to perform flow cytometry in order to show that TH2 inflammation will induce local macrophage proliferation B44to the paper
Anti-BrdU antibody was used for immunofluorescence, in order to study the mechanism by which Cry1/2 protect genomic integrity to the paper
Becton Dickinson anti-BrdU was used to perform immunohistochemistry in order to study the effect of histone supply on S phase timing and cell cycle progression to the paper
BD Pharmingen Flow BrdU kit was used to perform proliferation assays in order to study the oncogene-dependent apoptosis promoted by a component of the mir-17-92 polycistronic oncomir to the paper
BD Biosciences mouse monoclonal anti-BrdU antibody was used to perform immunohistochemistry in order to investigate the roles of Vav2 and Vav3 in skin cancer to the paper
BD BrdU Flow Kit was used to perform flow cytometry in order to investigate the importance of TCR signaling to natural killer T cell development to the paper
BD Biosciences BrdU staining kit was used to perform cell labeling in order to investigate the role of miR-146a in mouse hematopoietic stem cells to the paper
BD Biosciences FITC-conjugated anti-BrdU antibody was used to perform flow cytometry in order to investigate the regulatory effect of Ca2+ influx through TRPV4 cation channels on vascular function to the paper
BD Bioscience BrdU flow kit was used to perform cell cycle analysis in order to investigate the regulatory effect of PD-1 on IgA selection and the composition of the gut microflora to the paper
BD Pharmingen BrdU was used to perform cell cycle analysis in order to show that p53-dependent cell proliferation and survival could be regulated by atg7 to the paper
BD Biosciences BrdU flow kit was used to perform BrdU staining in order to show that lysosome function and macrophage homeostasis were disrupted without ENT3 to the paper
BD Pharmingen anti-BrdU was used to perform flow cytometry in order to show that antioxidant responses could be achieved by pyruvate kinase M2 inactivation to the paper
BD APC BrdU Flow Kit was used to perform immunohistochemistry in order to show that cell fate choice could be modulated by chromatin "prepattern" and histone modifiers to the paper
BD Bioscience anti-BrdU antibody was used to carry out immunofluorescence assays in order to investigate the role for CHBP protein from Burkholderia pseudomallei as a potent inhibitor of the eukaryotic ubiquitination pathway to the paper
BD Biosciences anti-BrdU antibody (1:25) was used in immunohistochemistry in order to demonstrate C/EBPalpha and C/EBPbeta are essential for sebocyte differentiation and epidermal squamous differentiation in adult mouse skin to the paper
BD Pharmingen BrdU was used to perform BrdU proliferation assays in order to show macrophages that expresses arginase-1 can suppress the inflammation and fibrosis induced by Th2 cytokine to the paper
BD Biosciences BrdU was used to evaluate T cell proliferation in order to show that the mice with decay-accelerating factor-deficient T cells can develop focal and segmental glomerulosclerosis easily to the paper
BD mouse monoclonal anti-BrdU antibody was used in immunofluorescence staining to conduct sectioned tissue in order to conform Sfrp regulation of Wnt5a signaling controls oriented cell division to develop the gut epithelium to the paper
BD BrdU was used to treat cells in order to study the role for NBA1 in IR resistance, cell cycle regulation, and the recruitment of BRCA1 to sites of DNA damage to the paper
Becton Dickinson anti-BrdU antibody was used to carry out immunohistochemical analysis in order to investigate the regulation of cytoprotective factors and cell proliferation by intestinal epithelial TAK1 signaling to the paper
BD anti-alpha-BrdU antibody was used to perform ChIP assays in order to study the regulation effect of cyclin A-cdk1 to the paper
BD Pharmingen BrdU was used to inject intraperitoneally into mice in order to emphasize the importance of the calcineurin-NFAT-Egr2 pathway in the development of the NKT lymphocyte lineage to the paper
Becton Dickinson BrdU antibody was used in immunohistochemistry in order to demonstrate that the brain tuberous sclerosis complex (TSC) can be caused by the loss of function of Tsc2 in radial glia to the paper
BD PharMingen BrdU Flow kit was used to assay CD4+ T-cell proliferation in vitro by measuring BrdU incorporation in order to investigate the role of PKC in the regulation of Th2 establishment and allergic airway inflammation in vivo to the paper
BD Bioscience BrdU detection kit was used for immunostained in order to study the effect of Zinc finger protein ZBTB20 on alpha-fetoprotein gene transcription in liver to the paper
BD Pharmingen FITC BrdU Flow Kit was used in flow cytometry in order to determine the functional significance of c-Myc regulation of nucleotide metabolism to the paper
Calbiochem anti-BrdU antibody was used to detect BrdU in immunohistochemistry in order to reveal viral oncoprotein E6 regulates the expression of tumor-suppressive miR-34a in cervical cancer-derived cell lines containing oncogenic HPVs to the paper
Calbiochem BrdU immunohistochemistry System was used to perform staining in order to study the function of C/EBP beta transactivated by p57Kip2 in changing chondrocytes from proliferation to hypertrophic differentiation to the paper
Developmental Studies Hybridoma Bank
DSHB anti-BrdU antibody was used to perform immunohistochemistry in order to study the role of E2f3b in myogenic differentiation to the paper
Developmental Studies Hybridoma Bank anti-BrdU antibody was used in immunohistochemistry to study E-catenin connects cell-density dependent adherens junctions with the developmental hedgehog pathway to the paper
Articles Reviewed
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  29. House J, Zhu S, Ranjan R, Linder K, Smart R. C/EBPalpha and C/EBPbeta are required for Sebocyte differentiation and stratified squamous differentiation in adult mouse skin. PLoS ONE. 2010;5:e9837 pubmed publisher
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  37. Matsuyama M, Aizawa S, Shimono A. Sfrp controls apicobasal polarity and oriented cell division in developing gut epithelium. PLoS Genet. 2009;5:e1000427 pubmed publisher
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  39. Roybon L, Hjalt T, Stott S, Guillemot F, Li J, Brundin P. Neurogenin2 directs granule neuroblast production and amplification while NeuroD1 specifies neuronal fate during hippocampal neurogenesis. PLoS ONE. 2009;4:e4779 pubmed publisher
  40. Scorah J, McGowan C. Claspin and Chk1 regulate replication fork stability by different mechanisms. Cell Cycle. 2009;8:1036-43 pubmed
  41. Wang B, Hurov K, Hofmann K, Elledge S. NBA1, a new player in the Brca1 A complex, is required for DNA damage resistance and checkpoint control. Genes Dev. 2009;23:729-39 pubmed publisher
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  46. Hirata M, Kugimiya F, Fukai A, Ohba S, Kawamura N, Ogasawara T, et al. C/EBPbeta Promotes transition from proliferation to hypertrophic differentiation of chondrocytes through transactivation of p57. PLoS ONE. 2009;4:e4543 pubmed publisher
  47. Katsuno Y, Suzuki A, Sugimura K, Okumura K, Zineldeen D, Shimada M, et al. Cyclin A-Cdk1 regulates the origin firing program in mammalian cells. Proc Natl Acad Sci U S A. 2009;106:3184-9 pubmed publisher
  48. Lazarevic V, Zullo A, Schweitzer M, Staton T, Gallo E, Crabtree G, et al. The gene encoding early growth response 2, a target of the transcription factor NFAT, is required for the development and maturation of natural killer T cells. Nat Immunol. 2009;10:306-13 pubmed publisher
  49. Canettieri G, Coni S, Della Guardia M, Nocerino V, Antonucci L, Di Magno L, et al. The coactivator CRTC1 promotes cell proliferation and transformation via AP-1. Proc Natl Acad Sci U S A. 2009;106:1445-50 pubmed publisher
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  51. Yang J, Leitges M, Duran A, Diaz Meco M, Moscat J. Loss of PKC lambda/iota impairs Th2 establishment and allergic airway inflammation in vivo. Proc Natl Acad Sci U S A. 2009;106:1099-104 pubmed publisher
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  53. Wang X, Rao R, Kosakowska Cholody T, Masood M, Southon E, Zhang H, et al. Mitochondrial degeneration and not apoptosis is the primary cause of embryonic lethality in ceramide transfer protein mutant mice. J Cell Biol. 2009;184:143-58 pubmed publisher
  54. Asp P, Acosta Alvear D, Tsikitis M, van Oevelen C, Dynlacht B. E2f3b plays an essential role in myogenic differentiation through isoform-specific gene regulation. Genes Dev. 2009;23:37-53 pubmed publisher
  55. Houshmandi S, Emnett R, Giovannini M, Gutmann D. The neurofibromatosis 2 protein, merlin, regulates glial cell growth in an ErbB2- and Src-dependent manner. Mol Cell Biol. 2009;29:1472-86 pubmed publisher
  56. Lorts A, Schwanekamp J, Elrod J, Sargent M, Molkentin J. Genetic manipulation of periostin expression in the heart does not affect myocyte content, cell cycle activity, or cardiac repair. Circ Res. 2009;104:e1-7 pubmed publisher
  57. Gurung A, Uddin F, Hill R, Ferguson P, Alman B. Beta-catenin is a mediator of the response of fibroblasts to irradiation. Am J Pathol. 2009;174:248-55 pubmed publisher
  58. Zhang W, Zhao J, Chen L, Urbanowicz M, Nagasaki T. Abnormal epithelial homeostasis in the cornea of mice with a destrin deletion. Mol Vis. 2008;14:1929-39 pubmed
  59. Liebig T, Erasmus J, Kalaji R, Davies D, Loirand G, Ridley A, et al. RhoE Is required for keratinocyte differentiation and stratification. Mol Biol Cell. 2009;20:452-63 pubmed publisher
  60. Liu A, Gotlieb A. Transforming growth factor-beta regulates in vitro heart valve repair by activated valve interstitial cells. Am J Pathol. 2008;173:1275-85 pubmed publisher
  61. Barron M, Brookes S, Draper C, Garrod D, Kirkham J, Shore R, et al. The cell adhesion molecule nectin-1 is critical for normal enamel formation in mice. Hum Mol Genet. 2008;17:3509-20 pubmed publisher
  62. Xie Z, Zhang H, Tsai W, Zhang Y, Du Y, Zhong J, et al. Zinc finger protein ZBTB20 is a key repressor of alpha-fetoprotein gene transcription in liver. Proc Natl Acad Sci U S A. 2008;105:10859-64 pubmed publisher
  63. Liu Y, Li F, Handler J, Huang C, Xiang Y, Neretti N, et al. Global regulation of nucleotide biosynthetic genes by c-Myc. PLoS ONE. 2008;3:e2722 pubmed publisher
  64. Manuel M, Pratt T, Liu M, Jeffery G, Price D. Overexpression of Pax6 results in microphthalmia, retinal dysplasia and defective retinal ganglion cell axon guidance. BMC Dev Biol. 2008;8:59 pubmed publisher
  65. Czaja K, Burns G, Ritter R. Capsaicin-induced neuronal death and proliferation of the primary sensory neurons located in the nodose ganglia of adult rats. Neuroscience. 2008;154:621-30 pubmed publisher
  66. Schuller H, Al Wadei H, Majidi M. Gamma-aminobutyric acid, a potential tumor suppressor for small airway-derived lung adenocarcinoma. Carcinogenesis. 2008;29:1979-85 pubmed publisher
  67. Rendl M, Polak L, Fuchs E. BMP signaling in dermal papilla cells is required for their hair follicle-inductive properties. Genes Dev. 2008;22:543-57 pubmed publisher
  68. Fueger P, Schisler J, Lu D, Babu D, Mirmira R, Newgard C, et al. Trefoil factor 3 stimulates human and rodent pancreatic islet beta-cell replication with retention of function. Mol Endocrinol. 2008;22:1251-9 pubmed publisher
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