在线日韩日本国产亚洲丨少妇伦子伦情品无吗丨欧美性猛交xxxx免费看蜜桃丨精品人妻系列无码一区二区三区丨亚洲精品无码不卡在线播放

Your Good Partner in Biology Research

FTL Antibody, Biotin conjugated

  • 中文名稱:
    FTL兔多克隆抗體, Biotin偶聯
  • 貨號:
    CSB-PA11409D0Rb
  • 規格:
    ¥880
  • 其他:

產品詳情

  • 產品名稱:
    Rabbit anti-Homo sapiens (Human) FTL Polyclonal antibody
  • Uniprot No.:
  • 基因名:
  • 別名:
    Ferritin L chain antibody; Ferritin L subunit antibody; Ferritin light chain antibody; Ferritin light polypeptide antibody; ferritin light polypeptide like 3 antibody; FRIL_HUMAN antibody; FTL antibody; LFTD antibody; NBIA 3 antibody; NBIA3 antibody
  • 宿主:
    Rabbit
  • 反應種屬:
    Human
  • 免疫原:
    Recombinant Human Ferritin light chain protein (2-175AA)
  • 免疫原種屬:
    Homo sapiens (Human)
  • 標記方式:
    Biotin
  • 克隆類型:
    Polyclonal
  • 抗體亞型:
    IgG
  • 純化方式:
    >95%, Protein G purified
  • 濃度:
    It differs from different batches. Please contact us to confirm it.
  • 保存緩沖液:
    Preservative: 0.03% Proclin 300
    Constituents: 50% Glycerol, 0.01M PBS, PH 7.4
  • 產品提供形式:
    Liquid
  • 應用范圍:
    ELISA
  • Protocols:
  • 儲存條件:
    Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
  • 貨期:
    Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.
  • 用途:
    For Research Use Only. Not for use in diagnostic or therapeutic procedures.

產品評價

靶點詳情

  • 功能:
    Stores iron in a soluble, non-toxic, readily available form. Important for iron homeostasis. Iron is taken up in the ferrous form and deposited as ferric hydroxides after oxidation. Also plays a role in delivery of iron to cells. Mediates iron uptake in capsule cells of the developing kidney.
  • 基因功能參考文獻:
    1. Mossbauer spectra of human liver ferritin and its pharmaceutical analogues Ferrum Lek and Maltofer(R) measured at various temperatures, are reported. PMID: 27372204
    2. Determining serum ferritin is a convenient and nonexpensive method to determine the outcome of the treatment of the cases with oral squamous cell carcinoma . Its potential as prognostic marker could not be overlooked PMID: 28862225
    3. The functional significance of the observed patch of carboxylate side chains and resulting metallocluster for biomineralization emerges from the lower iron oxidation rate measured in the E60AE61AE64A variant of human L-ferritin, leading to the proposal that the observed metallocluster corresponds to the suggested, but yet unobserved, nucleation site of L-ferritin PMID: 28202724
    4. The clinical measurement of ferritin in cerebrospinal fluid is a better biomarker than serum levels of ferritin for diagnosing and assessing the progression of amyotrophic lateral sclerosis patients. PMID: 27804118
    5. Our patient's transferrin saturation was 27% and HFE analysis revealed that she had neither H63D nor C282Y mutations that are known to predispose to hemochromatosis. Besides being an iron storage protein, ferritin is also one of the so-called acute phase proteins PMID: 28636169
    6. This is the first Australian report of the c.-167 C>T mutation in a large family with multiple affected individuals. PMID: 27096259
    7. Baseline serum ferritin (SF) did not influence bloodstream infections (BSIs), but higher levels resulted in more invasive fungal infections (IFIs) PMID: 28585071
    8. High serum ferritin expression is associated with metabolic syndrome. PMID: 27390880
    9. Hepatitis E virus ORF1 encoded macro domain protein interacts with light chain subunit of human ferritin and inhibits its secretion. PMID: 27170377
    10. indicate an important role of ferritin light chains in neurodegeneration PMID: 26994418
    11. This study demostrated that FTL mutation progressive brain iron dysregulation, morphological signs of early neurodegeneration and motor coordination deficits show PMID: 25447222
    12. FTL expression was higher in glioblastoma than in low-grade glioma, and decreased expression of FTL correlated with increased survival in glioblastoma patients. PMID: 26871431
    13. FTL gene mutation and persistent hyperferritinemia without iron deficiency anemia after phlebotomy PMID: 25720123
    14. Ferritin plasma levels increased significantly following stem cell transplantation in graft rejection patients. PMID: 26611853
    15. Single nucleotide polymorphisms in HAMP, BMP2, FTL and SLC40A1 genes have phenotype-modifying roles in hereditary hemochromatosis type 1. PMID: 25976471
    16. Genome-wide association study identifies variants in PMS1 associated with serum ferritin in a Chinese population. PMID: 25162662
    17. Urine ferritin levels are elevated significantly in systemic lupus erythematosus and correlate with disease activity. PMID: 22871034
    18. findings expand the genetic and clinical diversity of neuroferritinopathy and suggest CSF ferritin levels as a novel potential biochemical marker for the diagnosis of neuroferritinopathy. PMID: 24825732
    19. Plasma hepcidin-25 and ferritin light chain levels correlate with a malignant breast cancer diagnosis. PMID: 24306042
    20. provide a new mechanism for selective autophagy of ferritin and reveal a previously unappreciated role for autophagy and NCOA4 in the control of iron homeostasis in vivo PMID: 25327288
    21. Genetic testing confirmed the diagnosis of hereditary hyperferritinemia cataract syndrome (HHCS), demonstrating a C39>G (c.-161C>G) mutation into FTL gene. PMID: 24983587
    22. A c.-171C>G mutation in the iron-regulatory element of FTL was found in 2 members of a Spanish family with hyperferritinemia-cataract syndrome. PMID: 24022025
    23. Elevated cerebrospinal ferritin reliably (but unspecifically) indicates severe central nervous system disease. PMID: 24821637
    24. Through combining serum ferritin and MS spectral data, the diagnosis sensitivity and specificity of our model for prewarning severe aGVHD (III~IV degrees aGVHD) before transplant all increased to 90.0% PMID: 24195075
    25. Increased levels of ferritin light chain protein is associated with breast cancer. PMID: 23969999
    26. Together, our results suggest that iron can increase gamma-secretase activity through promoting the level of FTL that interacts with and stabilizes PEN-2 PMID: 23685131
    27. Elevated levels of ferritin are associated with type 2 diabetes mellitus. PMID: 23381919
    28. Data show the transcriptional regulation of the human ferritin gene by coordinated regulation of Nrf2 and protein arginine methyltransferases PRMT1 and PRMT4. PMID: 23699174
    29. Noncoding G-to-T transversion (c.-168G>T) located in the iron response element (IRE) of the gene coding for ferritin light chain (FTL) cosegregated with cataract in the family. PMID: 23592921
    30. The Badalona 36C > U and Heidelberg 52 G > C mutations within the L-ferritin Iron-Responsive Element only mildly alter the binding capacity of the Iron Regulatory Proteins but are still causative for hyperferritinaemia cataract syndrome. PMID: 23421845
    31. Elevation in ferritin is associated with response to trastuzumab in breast cancer. PMID: 23300545
    32. Plasma levels of FLT and S100A9 proteins are up-regulated and CNDP1 levels are down-regulated in patients with glioblastoma. PMID: 23029420
    33. data demonstrate an enhanced propensity of mutant ferritin to undergo iron-catalyzed oxidative damage and support this as a mechanism causing disruption of ferritin structure and iron mishandling that contribute to pathology of hereditary ferritinopathy PMID: 22348978
    34. Two novel missense L-ferritin variants are associated with hyperglycosylation, p.Gln26Ile and p.Ala27Val, and with benign hyperferritinemia in two unrelated patients. PMID: 22535864
    35. High ferritin is associated with poor treatment response in hematological neoplasms. PMID: 22248276
    36. The data strongly suggest that FTL and SCCA1 may serve as coreceptors in HBV cellular attachment and virus entry into hepatocytes. PMID: 22359459
    37. Molecular genetic analysis revealed point mutations within the FTL IRE. PMID: 22020773
    38. genetic variations in the HFE gene, but not plasma ferritin may have a role in coronary heart disease in Chinese PMID: 21696736
    39. Genetic analysis revealed mutation G32A in Pedigree 1 and mutation G32T in Pedigree 2, both heterozygous and located in the iron-responsive element of the ferritin light chain mRNA in hyperferritinemia cataract syndrome. PMID: 21907119
    40. FTL is a target gene of the BACH1 transcription factor according to ChIP-seq analysis in HEK 293 cells. PMID: 21555518
    41. In the family with hyperferritinemia cataract syndrome a G-->C heterozygous mutation at position +32 of FTL was identified. PMID: 21541272
    42. Somatic mutations in the iron response elements (IRE) of the L-ferritin gene are infrequent in the age-related cataract. PMID: 21139976
    43. This protein has been found differentially expressed in thalami from patients with schizophrenia. PMID: 20471030
    44. Toluene diisocyanate (TDI) regulates haem oxygenase-1/ferritin expression: implications for toluene diisocyanate-induced asthma. PMID: 20345975
    45. biochemical and crystallographic characterization of pathogenic FTL mutant p.Phe167SerfsX26 showing that it is a functional ferritin with an altered conformation of the C terminus PMID: 20159981
    46. This protein has been found differentially expressed in the anterior cingulate cortex from patients with schizophrenia PMID: 20381070
    47. indicate that cellular iron imbalance and oxidative damage produced by the over-expression in of two pathogenic L-ferritin variants are primary causes of cell death, while aggregate formation is a secondary effect PMID: 19781644
    48. the x-ray crystallographic structure and report functional studies of ferritin homopolymers formed from the mutant FTL polypeptide PMID: 19923220
    49. Finding not only supports direct evidence for a regulatory role of L-ferritin in neuroectodermal cell pigmentation but also integrates a new player within a complicated network governing iron homeostasis in the dopamine neurons of substantia nigra. PMID: 19318681
    50. The genetic defects in the FTL gene are unlikely to be a common cause of typical PD, at least in a North America population. PMID: 12459518

    顯示更多

    收起更多

  • 相關疾病:
    Hyperferritinemia with or without cataract (HRFTC); Neurodegeneration with brain iron accumulation 3 (NBIA3); L-ferritin deficiency (LFTD)
  • 蛋白家族:
    Ferritin family
  • 數據庫鏈接:

    HGNC: 3999

    OMIM: 134790

    KEGG: hsa:2512

    STRING: 9606.ENSP00000366525

    UniGene: Hs.433670



主站蜘蛛池模板: 精品香蕉久久久午夜福利| 插插插精品亚洲一区| 无码纯肉动漫在线观看| 国产成人av性色在线影院色戒| 亚洲伊人久久精品影院| 青青草视频在线观看| 一出一进一爽一粗一大视频| 日日噜噜夜夜狠狠久久蜜桃| 无线日本视频精品| 成人免费无码不卡毛片视频| 久久大香国产成人av| .精品久久久麻豆国产精品| 欧美疯狂性受xxxxx喷水| 成年午夜精品久久久精品| 亚洲日韩看片无码超清| 手机真实国产乱子伦对白视频| 久久精品无码精品免费专区| 婷婷四房色播| 无码人妻aⅴ一区二区三区玉蒲团| 精品国内自产拍在线观看| 亚洲老熟女av一区二区在线播放| 男女猛烈xx00免费视频试看| 人人妻人人藻人人爽欧美一区| 夜夜欢性恔免费视频| 亚洲国产欧美在线观看片不卡 | 一线二线三线天堂| 人人澡人摸人人添| 韩国午夜福利片在线| 欧美写真视频在线观看| 色婷婷综合中文久久一本 | 亚洲欧美日本久久综合网站| 人妻出差精油按摩被中出| 18禁无遮挡啪啪无码网站| 国产免费又爽又色又粗视频| 色综合久久久久无码专区| 精品服丝袜无码视频一区| 免费国产线观看免费观看| 亚洲精品色午夜无码专区日韩| 国产偷抇久久精品a片69| 亚洲成a人v欧美综合天堂下载| 免费无码又爽又刺激激情视频软件 |