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Human A disintegrin and metalloproteinase with thrombospondin motifs 9(ADAMTS9) ELISA kit

  • 中文名稱:
    人A解聚素和金屬蛋白酶及血小板反應蛋白基序9(ADAMTS9)酶聯免疫試劑盒
  • 貨號:
    CSB-EL001316HU
  • 規格:
    96T/48T
  • 價格:
    ¥3600/¥2500
  • 其他:

產品詳情

  • 產品描述:
    人A解聚素和金屬蛋白酶及血小板反應蛋白基序9(ADAMTS9)酶聯免疫試劑盒(CSB-EL001316HU)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ADAMTS9含量。ADAMTS9是一種具有血小板反應蛋白基序的ADAM金屬肽酶,編碼ADAMTS蛋白家族成員。該家族成員共享多個蛋白質模塊,包括前肽區域、金屬蛋白酶結構域等,參與蛋白聚糖裂解、器官形狀控制及血管生成抑制。研究機制涉及ADAMTS9與蛋白聚糖、細胞外基質等相互作用,以及其在多種疾病如遺傳性腎腫瘤、早產胎膜早破等中的作用。試劑盒檢測范圍為0.78 ng/mL-50 ng/mL,適用于體外培養細胞模型中蛋白酶分泌機制研究、疾病動物模型組織內源性ADAMTS9水平檢測,以及通過臨床前樣本(如血清、血漿)探索其與特定病理過程的相關性,為探究ADAMTS9在組織修復、血管生成及代謝調控中的分子機制提供可靠的科研工具。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:
    ADAMTS9 ELISA Kit; KIAA1312 ELISA Kit; A disintegrin and metalloproteinase with thrombospondin motifs 9 ELISA Kit; ADAM-TS 9 ELISA Kit; ADAM-TS9 ELISA Kit; ADAMTS-9 ELISA Kit; EC 3.4.24.- ELISA Kit
  • 縮寫:
    ADAMTS9
  • Uniprot No.:
  • 種屬:
    Homo sapiens (Human)
  • 樣本類型:
    serum, plasma, cell culture supernates, tissue homogenates
  • 檢測范圍:
    0.78 ng/mL-50 ng/mL
  • 靈敏度:
    0.195 ng/mL
  • 反應時間:
    1-5h
  • 樣本體積:
    50-100ul
  • 檢測波長:
    450 nm
  • 研究領域:
    Cell Biology
  • 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 human ADAMTS9 in various matrices and diluted with the Sample Diluent to produce samples with values within the dynamic range of the assay.
     SampleSerum(n=4)
    1:5Average %90
    Range %85-96
    1:10Average %95
    Range %91-100
    1:20Average %92
    Range %86-98
    1:40Average %90
    Range %86-98
  • 回收率:
    The recovery of human ADAMTS9 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) 10097-106
    EDTA plasma (n=4)8794-93
  • 標準曲線:
    These standard curves are provided for demonstration only. A standard curve should be generated for each set of samples assayed.
    ng/mlOD1OD2AverageCorrected
    502.500 2.488 2.494 2.398
    251.458 1.376 1.417 1.321
    12.50.717 0.684 0.701 0.605
    6.250.358 0.339 0.349 0.253
    3.120.227 0.214 0.221 0.125
    1.560.161 0.159 0.160 0.064
    0.780.126 0.118 0.122 0.026
    00.097 0.095 0.096  
  • 數據處理:
  • 貨期:
    3-5 working days

產品評價

靶點詳情

  • 功能:
    Cleaves the large aggregating proteoglycans, aggrecan (at the '1838-Glu-|-Ala-1839' site) and versican (at the '1428-Glu-|-Ala-1429' site). Has a protease-independent function in promoting the transport from the endoplasmic reticulum to the Golgi apparatus of a variety of secretory cargos.
  • 基因功能參考文獻:
    1. ADAMTS9 gene cytosine-adenine repeat polymorphism may be used to determine the prognosis for knee osteoarthritis radiologic progression. PMID: 27230574
    2. expression by synovial cells induced by hemoglobin at low doses, suggesting a possible role for hemoglobin in cartilage damage after intra-articular hemorrhage PMID: 29137610
    3. By inhibiting ADAMTS-9, miR-338-5p suppressed the proliferation and metastasis of rheumatoid arthritis synovial fibroblasts. PMID: 28850027
    4. Exogenous expression of ADAMTS9 in colorectal cancer cell lines inhibited cell proliferation and migration through the regulation of cell cycle and apoptosis. PMID: 29186710
    5. Our data showed that four SNPs (rs73832338, rs9985304, rs4317088, and rs9831846) in the ADAMTS9 gene were significantly associated with cognitive aging among the subjects. Additionally, we found that interactions between the ADAMTS9 rs9985304 and ADAMTS9 rs76346246 SNPs influenced cognitive aging. PMID: 28225792
    6. we identified the top 10 highly differentiated SNPs in Brazilian Amerindian ancestry compared to Asian, European, and African Genomes.SNPs within or proximal to CIITA (rs6498115), SMC6 (rs1834619), and KLHL29 (rs2288697) were most differentiated in the Amerindian-specific branch. SNPs in ADAMTS9 (rs7631391), DOCK2 (rs77594147), SLC28A1 (rs28649017), ARHGAP5 (rs7151991), and CIITA (rs45601437) in the Asian comparison. PMID: 28100790
    7. study identified a suggestive genome-wide significant association of ADAMTS9 with asthma in Spanish subjects PMID: 26620591
    8. NF-kappaBp65 bound to elements located at -1177 and -1335 in the ADAMTS9 promoter region, in contrast to the untreated samples. The results of the present study suggested that NF-kappaB may be involved in IL-1beta-induced activation of ADAMTS9 in human chondrocytes PMID: 25760020
    9. A deletion at ADAMTS9-MAGI1 locus is associated with psoriatic arthritis risk. PMID: 25990289
    10. LncRNA ADAMTS9-AS2 is regulated by DNMT1 and inhibits migration of glioma cells. PMID: 24833086
    11. The present study reveals ADAMT-9 expression by mast cells(MCs) and that MC activation regulates the expression of the protease, thus implicating the ADAMT-9 of protease in MC function. PMID: 23154421
    12. The pathways MAPK and NF-kappaB were responsible pathways for the induction of ADAMTS9 gene. PMID: 23175174
    13. PPARG2 and ADAMTS9 variants are both associated with type 2 diabetes mellitus and with insulin resistance, whereas only ADAMTS9 may be related to beta cell function. PMID: 23161442
    14. ADAMTS9 acts as a functional tumor suppressor in gastric cancer through inhibiting oncogenic AKT/mTOR signaling pathway PMID: 22907434
    15. ADAMTS9 and GON-1 in the ER that promotes protein transport from the ER to the Golgi. This function is GON-domain dependent but protease activity independent. PMID: 22419820
    16. Data show that the expression of ADAMTS4, 9, 16 and was up-regulated during chondrogenesis, ADAMTS1 and 5 were down-regulated. PMID: 22562232
    17. four of the six aggrecanases are expressed in immortalized chondrocyte cell-lines and can be upregulated in response to inflammatory cytokines PMID: 20568084
    18. Results indicate that ADAMTS9 contributes an important function in the tumor microenvironment that acts to inhibit angiogenesis and tumor growth in both esophageal cancer and nasophageal cancer. PMID: 20551050
    19. These data identify ADAMTS9 as a novel, constitutive, endogenous angiogenesis inhibitor that operates cell-autonomously in endothelial cells. PMID: 20093484
    20. These data identify for the first time the cellular chaperones associated with secretion of an ADAMTS protease and suggest a role for gp96 in modulating pro-ADAMTS9 processing. PMID: 19875450
    21. ancillary domains of ADAMTS-9 are required both for specific extracellular localization and for its versicanase and aggrecanase activities PMID: 12514189
    22. negative effect of TGFbeta1 on ADAMTS-1, -5, -9, and -15 coupled with increases in their inhibitor, TIMP-3 may aid the accumulation of versican in the stromal compartment of the prostate in BPH and prostate cancer PMID: 15599946
    23. TSR-1 domain-bearing truncated ADAMTS-9 demonstrates positive GAG-binding ability & displayed low aggrecanase activity. PMID: 16507336
    24. pro-ADAMTS9 is processed at the cell surface by furin PMID: 16537537
    25. this study identifies and provides functional evidence for a critical region associated with tumor suppression on 3p14.2 and provides the first evidence that ADAMTS9, mapping to this region, may contribute to esophageal cancer development PMID: 16799631
    26. ADAMTS9 expression was downregulated or lost in 17 of 23 (73.9%) lymph node metastatic nasopharyngeal carcinoma (NPC) specimens. After transfection of the ADAMTS9 gene into 7 NPC cell lines, a dramatic reduction of colony forming ability was observed. PMID: 18449890
    27. Study show that polymorphisms in ADAMTS9 were associated with type 2 diabetes risk in the studied population. PMID: 18694974
    28. These findings may provide a better understanding of the NFATc1 regulation of ADAMTS9 expression induced by inflammatory cytokines such as IL-1 beta. PMID: 19052845
    29. present study is novel in evaluating the prevalence of ADAMTS9 methylation based on a large number of tumor samples and showing that epigenetic regulation of ADAMTS9 was associated with carcinogenesis PMID: 19963134

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  • 亞細胞定位:
    Secreted, extracellular space, extracellular matrix. Endoplasmic reticulum.
  • 組織特異性:
    Highly expressed in all fetal tissues. Expressed in a number of adult tissues with highest expression in heart, placenta and skeletal muscle.
  • 數據庫鏈接:

    HGNC: 13202

    OMIM: 605421

    KEGG: hsa:56999

    STRING: 9606.ENSP00000418735

    UniGene: Hs.656071



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