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Mouse fibroblast growth factor 10(FGF10) ELISA Kit

  • 中文名稱:
    小鼠成纖維細胞生長因子10(FGF10)酶聯免疫試劑盒
  • 貨號:
    CSB-E13045m
  • 規格:
    96T/48T
  • 價格:
    ¥3600/¥2500
  • 其他:

產品詳情

  • 產品描述:
    小鼠成纖維細胞生長因子10(FGF10)酶聯免疫試劑盒(CSB-E13045m)為雙抗夾心法ELISA試劑盒,定量檢測血清、血漿、組織培養上清液、組織勻漿樣本中的FGF10含量。FGF10,也稱為成纖維細胞生長因子10,是一種肝素結合生長因子,屬于FGF家族。它在多種生物過程中發揮重要作用,包括胚胎發育、細胞生長、形態發生、組織修復和腫瘤生長。FGF10通過與其受體FGFR結合,激活信號通路,從而影響細胞增殖、分化和遷移。研究顯示,FGF10在心臟修復、脂肪生成和器官形態發生中具有關鍵作用。試劑盒檢測范圍為1.56 pg/mL-100 pg/mL,可廣泛應用于細胞因子分泌研究、組織微環境分析、疾病模型建立等科研領域,尤其適用于發育生物學、再生醫學及炎癥相關機制研究中的FGF10動態監測。本品僅用于科研,不用于臨床診斷,產品具體參數及操作步驟詳見產品說明書。
  • 別名:
    Fgf10Fibroblast growth factor 10 ELISA Kit; FGF-10 ELISA Kit; Keratinocyte growth factor 2 ELISA Kit
  • 縮寫:
  • Uniprot No.:
  • 種屬:
    Mus musculus (Mouse)
  • 樣本類型:
    serum, plasma, cell culture supernates, tissue homogenates
  • 檢測范圍:
    1.56 pg/mL-100 pg/mL
  • 靈敏度:
    0.39 pg/mL
  • 反應時間:
    1-5h
  • 樣本體積:
    50-100ul
  • 檢測波長:
    450 nm
  • 研究領域:
    Cardiovascular
  • 測定原理:
    quantitative
  • 測定方法:
    Sandwich
  • 精密度:
    Intra-assay Precision (Precision within an assay): CV%<8%
    Three samples of known concentration were tested twenty times on one plate to assess.
    Inter-assay Precision (Precision between assays): CV%<10%
    Three samples of known concentration were tested in twenty assays to assess.
  • 線性度:
    To assess the linearity of the assay, samples were spiked with high concentrations of mouse FGF10 in various matrices and diluted with the Sample Diluent to produce samples with values within the dynamic range of the assay.
    SampleSerum(n=4)
    1:1Average %96
    Range %90-102
    1:2Average %102
    Range %97-107
    1:4Average %89
    Range %86-92
    1:8Average %94
    Range %89-99
  • 回收率:
    The recovery of mouse FGF10 spiked to levels throughout the range of the assay in various matrices was evaluated. Samples were diluted prior to assay as directed in the Sample Preparation section.
    Sample TypeAverage % RecoveryRange
    Serum (n=5) 10398-108
    EDTA plasma (n=4)9590-110
  • 標準曲線:
    These standard curves are provided for demonstration only. A standard curve should be generated for each set of samples assayed.
    pg/mlOD1OD2AverageCorrected
    1002.194 2.345 2.270 2.102
    501.494 1.465 1.480 1.312
    250.889 0.967 0.928 0.760
    12.50.594 0.556 0.575 0.407
    6.250.384 0.383 0.384 0.216
    3.120.302 0.290 0.296 0.128
    1.560.212 0.225 0.219 0.051
    00.167 0.168 0.168
  • 數據處理:
  • 貨期:
    3-5 working days

產品評價

靶點詳情

  • 功能:
    Plays an important role in the regulation of embryonic development, cell proliferation and cell differentiation. Required for normal branching morphogenesis. May play a role in wound healing.
  • 基因功能參考文獻:
    1. It is concluded that during early pseudoglandular stage of lung development Ptch1 patterns Fgf10 and regulates Foxf1 expression in the lung mesenchyme to direct branch formation and this is essential for proper lobe formation and lung function. PMID: 28939119
    2. small interfering RNA knockdown of FGFR2 suppressed PI3K/Akt pathway activation by FGF10 and abolished its anti-apoptotic and neurite repair effects in vitro. PMID: 28981091
    3. the response of FGF10(+) progenitors and differentiated Airway smooth muscle cells to growth factor treatment in real time using lineage tracing in the background of an air-liquid interface (ALI) culture system. PMID: 28387977
    4. Inactivation of ALX4/Alx4 causes lacrimal gland aplasia in both human and mouse. These results reveal a key role of Alx4 in mediating FGF-Shp2-FGF signaling in the neural crest for lacrimal gland development. PMID: 29028795
    5. show that during homeostasis, basal stem/progenitor cells in cartilaginous airways maintain their stem cell state by downregulating the Hippo pathway (resulting in increased nuclear Yap), which generates a localized Fgf10-expressing stromal niche PMID: 29017029
    6. that miR-205 in the surface ectoderm functions to ensure robust activation of pathways associated with Fgf10 signaling. PMID: 28511845
    7. Mesenchymal FGF10 controls the size of the taste bud papillary area, while overall patterning remains unchanged. Results show that FGF signaling negatively affects the extent of canonical Wnt signaling, which is the main activation pathway during fungiform papillae development; however, this effect does not occur at the level of gene transcription. PMID: 28506989
    8. Sox9 is positively regulated by mesenchymal Fgf10, a process that requires active Erk signaling during salivary gland development PMID: 28506998
    9. Fgf10 is expressed in the mesenchyme around developing submucosal glands. All nasal glands require FGF10 for branching morphogenesis. FGF10 is required for gland budding and ductal morphogenesis of the Steno's gland and the maxillary sinus glands. PMID: 27590203
    10. FGFR2c signaling regulates branching morphogenesis through the activation of FGFR2b signaling via increased FGF10 autocrine. These results provide new insight into the mechanisms by which crosstalk between FGFR2b and FGFR2c results in efficient branching morphogenesis. PMID: 27206683
    11. Decreased Fgf10 mRNA levels lead to congenital lung defects, which are compatible with postnatal survival, but which compromise the ability of the lungs to cope with sub-lethal hyperoxic injury. PMID: 27770432
    12. Fgf10 enhances the formation of tissue-engineered small intestine. PMID: 23468377
    13. Lhx9 expression overlapped markedly with FGF10 expression cells in the limb mesenchyme and was associated with proliferative cells of the progress zone. PMID: 26220830
    14. Hypoplasia of the salivary glands led to a significant reduction in saliva production in Fgf10 heterozygous adult mice PMID: 26321752
    15. Fgf10 signaling has an essential role in the formation of lipofibroblasts during late lung development PMID: 26511927
    16. novel allele of Alx4 results in reduced Fgf10 expression and failure of eyelid fusion in mice PMID: 25673119
    17. regulates regional cardiomyocyte proliferation in the foetal heart through a FOXO3/p27(kip1) pathway PMID: 25344367
    18. Fgf10 alters epithelial cell differentiation in the small intestinal mucosa. PMID: 25721301
    19. Fgf10 plays a dual role in cochlear development: to regulate outgrowth of the duct and subsequently as a bidirectional signal that sequentially specifies Reissners membrane and outer sulcus non-sensory domains. PMID: 25624266
    20. FGF10 has a role in protecting neuron against oxygen-glucose deprivation injury through inducing heme oxygenase-1 PMID: 25446127
    21. A signaling mechanism based on FGF10 and SHH directs outgrowth of the lung bud via a ligand-receptor-based Turing mechanism and a geometry effect in the embryonic mouse. PMID: 25359721
    22. Results thus show how Pbx1 controls Fgf10 in the developing lung. PMID: 24591256
    23. Data identify autocrine activation of FGF signaling as an essential mechanism in promoting Pten-deficient skin tumors. PMID: 24582960
    24. apical ectodermal ridge-Fibroblast growth factors activate sub-apical ectodermal ridge mesenchymal Fgf10 transcription via the downstream Mek-Erk pathway, Etv1, and Ewsr1 in an AGAAAR cluster-dependent manner. PMID: 25109552
    25. FGF10 and FGF2 were identified as stromal ligands that control distinct aspects of mammary ductal branching. PMID: 25078648
    26. FGF10, which was produced from tumor cells, was essential for the proliferation of tumor cell itself and also supports proliferation of endothelial cells. PMID: 24320134
    27. Fgf10-expressing cells represent a pool of mesenchymal progenitors in the embryonic and postnatal lung. PMID: 24353064
    28. Fgf-10 and Fgf-18 are expressed specifically within ventral tanycyte subpopulations. PMID: 23804023
    29. Fgf10 prevents ciliated cell differentiation and promotes basal cell differentiation. PMID: 23924632
    30. inhibition of FGF-10 by inflammatory signaling involves the NF-kappaB-dependent interactions between RELA, SP3, and the Fgf-10 promoter. PMID: 23558680
    31. The sclera of myopic eyes had higher FGF10 levels. The risk G allele of SNP rs339501 was associated with extreme myopia in human and caused a higher gene expression in the luciferase assay. PMID: 23599340
    32. These studies provide direct evidence in support of hypothalamic neurogenesis during late postnatal and adult life, and identify Fgf10(+) tanycytes as a source of parenchymal neurons with putative roles in appetite and energy balance. PMID: 23554498
    33. the FGF10-FGFR2b signaling pathway is not required for epithelial proliferation and differentiation during adult glandular stomach homeostasis PMID: 23133671
    34. Gata3 directly activates Fgf10 in the early inner ear, and does so through a single binding site PMID: 23220102
    35. Fibroblast growth factor 10 gene regulation in the second heart field by Tbx1, Nkx2-5, and Islet1 reveals a genetic switch for down-regulation in the myocardium PMID: 23093675
    36. show that the Fgf10(iCre) line can be used for conditional gene inactivation in an inducible fashion during early developmental stages PMID: 22719891
    37. Results demonstrate that organ fate commitment and progenitor cell expansion are coordinately controlled by the activity of a Sox9/Fgf10/Fgfr2b feed-forward loop in the pancreatic niche. PMID: 22874919
    38. Using tissue specific Fgf9 versus Pitx2 loss of function approaches in the gut epithelium and/or mesenchyme, we determined that FGF9 signals to the mesenchyme via Pitx2 to induce mesenchymal Fgf10 expression, which leads to epithelial cecal bud formation. PMID: 22819677
    39. GAG controls lacrimal gland induction by restricting the diffusion of Fgf10 PMID: 22745308
    40. [review] Preadipocyte proliferation and adipogenesis are greatly impaired in Fgf10 knockout mouse embryos. PMID: 21696361
    41. Functional analysis of Fgf signaling revealed precise reciprocal interactions, which showed that mesenchymal Fgf10 rather than Fgf7 modulates tongue epithelial differentiation via Fgfr2b in a temporal- and spatial-specific manner. PMID: 21720756
    42. deletion of Fgf10 led to absence of the CVP, identifying FGF10 as the first inductive, mesenchyme-derived factor for taste papillae PMID: 21655085
    43. Fgf3 and Fgf10 are not required for specification of cardiovascular progenitors, but rather for their normal developmental coordination. PMID: 21664901
    44. show that Wnt2 signaling is necessary and sufficient for activation of a transcriptional and signaling network critical for smooth muscle specification and differentiation including myocardin/Mrtf-B and the signaling factor Fgf10 PMID: 21704027
    45. Results identify a myocardial to epicardial fibroblast growth factor (FGF) signal, mediated by FGF10 and FGFR2b, that is essential for movement of cardiac fibroblasts into the compact myocardium. PMID: 21750042
    46. FGF-10 induced cardiomyocyte differentiation from ES cells and iPS cells, which may have potential for translation into clinical applications PMID: 21203390
    47. study proposes that Alk5 functions upstream of Fgf10 to regulate transit-amplifying cell proliferation and stem cell maintenance and that this signaling mechanism is crucial for stem cell-mediated tooth regeneration PMID: 21402782
    48. Fgf10-Fgfr2b signaling and lacrimal gland development are controlled by 2-O- and 6-O-sulfated heparan sulfate PMID: 21357686
    49. role of two crucial morphogens, fibroblast growth factor 10 and sonic hedgehog, in the formation of periodically alternating cartilaginous and non-cartilaginous domains in the ventral mesenchyme PMID: 21148187
    50. demonstrate that FGF10-signaling targets include ETS-family transcription factors, which have previously been shown to regulate epithelial maturation and tumor progression PMID: 20883684

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  • 亞細胞定位:
    Secreted.
  • 蛋白家族:
    Heparin-binding growth factors family
  • 組織特異性:
    Expressed abundantly in embryos and the lung, and at much lower levels in brain and heart.
  • 數據庫鏈接:


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