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

NRXN1 Antibody

  • 中文名稱:
    NRXN1兔多克隆抗體
  • 貨號:
    CSB-PA347832ESR2HU
  • 規格:
    ¥440
  • 圖片:
    • Immunohistochemistry of paraffin-embedded human brain tissue using CSB-PA347832ESR2HU at dilution of 1:100
  • 其他:

產品詳情

  • 產品名稱:
    Rabbit anti-Homo sapiens (Human) NRXN1 Polyclonal antibody
  • Uniprot No.:
  • 基因名:
  • 別名:
    DKFZp313P2036 antibody; FLJ35941 antibody; Hs.22998 antibody; KIAA0578 antibody; Neurexin 1 alpha antibody; Neurexin 1 beta antibody; Neurexin I-alpha antibody; Neurexin-1 antibody; Neurexin-1-alpha antibody; NRX1A_HUMAN antibody; NRXN1 antibody; PTHSL2 antibody; SCZD17 antibody
  • 宿主:
    Rabbit
  • 反應種屬:
    Human
  • 免疫原:
    Recombinant Human Neurexin-1 protein (31-310AA)
  • 免疫原種屬:
    Homo sapiens (Human)
  • 標記方式:
    Non-conjugated
  • 克隆類型:
    Polyclonal
  • 抗體亞型:
    IgG
  • 純化方式:
    Antigen Affinity Purified
  • 濃度:
    It differs from different batches. Please contact us to confirm it.
  • 保存緩沖液:
    PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
  • 產品提供形式:
    Liquid
  • 應用范圍:
    ELISA, IHC
  • 推薦稀釋比:
    Application Recommended Dilution
    IHC 1:20-1:200
  • 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:
    Cell surface protein involved in cell-cell-interactions, exocytosis of secretory granules and regulation of signal transmission. Function is isoform-specific. Alpha-type isoforms have a long N-terminus with six laminin G-like domains and play an important role in synaptic signal transmission. Alpha-type isoforms play a role in the regulation of calcium channel activity and Ca(2+)-triggered neurotransmitter release at synapses and at neuromuscular junctions. They play an important role in Ca(2+)-triggered exocytosis of secretory granules in pituitary gland. They may effect their functions at synapses and in endocrine cells via their interactions with proteins from the exocytotic machinery. Likewise, alpha-type isoforms play a role in regulating the activity of postsynaptic NMDA receptors, a subtype of glutamate-gated ion channels. Both alpha-type and beta-type isoforms may play a role in the formation or maintenance of synaptic junctions via their calcium-dependent interactions (via the extracellular domains) with neuroligin family members, CBLN1 or CBLN2. In vitro, triggers the de novo formation of presynaptic structures. May be involved in specification of excitatory synapses. Alpha-type isoforms were first identified as receptors for alpha-latrotoxin from spider venom.
  • 基因功能參考文獻:
    1. Dual mutations of NRXN1 and TP53 proteins are associated with different drug responses in gastric cancer. PMID: 27708434
    2. findings did not support a major role of prominent NRXN1 gene polymorphisms in tardive dyskinesia PMID: 28120489
    3. The results support the importance of exons near the 5' end of NRXN1 in the expression of neurodevelopmental disorders. Intronic NRXN1 deletions do not appear to substantially increase the risk for clinical phenotypes PMID: 27195815
    4. that alpha-Neurexin binding to alpha2delta of N-type calcium channels is a conserved mechanism for regulating synaptic transmission PMID: 28669545
    5. NRXN1 copy number variants (deletions) were associated with increased risk of Tourette syndrome. PMID: 28641109
    6. MDGAs regulate the formation of neuroligin-neurexin trans-synaptic bridges by sterically blocking access of neurexins to neuroligins. PMID: 28641112
    7. In a Mexican Mestizo population, greater consumption of cigarettes was influenced by polymorphisms in the NRXN1 and CHRNA5 genes. PMID: 27355804
    8. Results demonstrate that NRXN1 alternative isoform expression is temporally regulated during critical periods of human neocortical development and identify potential differential molecular contributions of NRXN1-alpha and -beta to schizophrenia and bipolar disorder PMID: 26216298
    9. the top-ranked discordances were subsequently selected for validation by quantitative polymerase chain reaction (qPCR), from which one single ~120kb deletion in NRXN1 on chromosome 2 (bp 51017111-51136802) was validated PMID: 26899349
    10. Atypical hand-foot-genital syndrome and developmental delay due to de novo mutations in HOXA13 and NRXN1 PMID: 26590955
    11. The rare variants in NRXN1 were significantly associated with smoking status. PMID: 25450229
    12. NRXN1 has an affinity for binding to LRRTM2 in hippocampal synapses. PMID: 26785044
    13. heterozygous inactivation of NRXN1 directly impairs synaptic function in human neurons. PMID: 26279266
    14. Increasing expression of TGF-beta1 protein, decreasing expressions of Ghrelin, Neurexin, and Neuroligin proteins can induce the loss or dysfunction of ganglion cells in distal intestinal canal PMID: 25399301
    15. Results indicate that the neurexin and neuroligin synaptic complex is intrinsically involved in the regulation of DISC1 function, thus contributing to a better understanding of the pathology of schizophrenia. PMID: 26078884
    16. Study suggests a role of rare missense variants at NRXN1 and AKAP9 in schizophrenia susceptibility, probably related to alteration of the excitatory/inhibitory synaptic balance, deserving further investigation PMID: 25943950
    17. The phenotype found in the microdeletions of alpha exons of the NRXN1 gene is clearly distinguishable from the one found in the microdeletions of beta exons, with macrocephaly, epilepsy and mental retardation. PMID: 25710691
    18. The role of NRXN1 in in paranoid schizophrenia development in Russians. PMID: 26410934
    19. A further patient with a biallelic homozygous deletion in NRXN1 is reported here. PMID: 25486015
    20. study did not find any of the 4 mutations identified in patients meeting the diagnostic criteria for autism with intellectual disability in either the schizophrenia patient group or the control group despite expected genetic overlap among autism, intellectual disability and schizophrenia PMID: 25242362
    21. Mutation screening of the NRXN1gene in patients with ID and ASD may be useful to identify potential variants predisposing to ID and ASD PMID: 24832020
    22. Study provides statistically significant evidence of association of NRXN1 rs12467557 and rs10490162 with atypical antipsychotic treatment response in a placebo-controlled, in-patient treatment response study PMID: 24633560
    23. This study demonistrated that NRXN1 deletions are more frequent in patients with schizophrenia than in healthy individuals. PMID: 24680031
    24. study identified a homozygous mutation in RBBP8, which co-segregates with microcephaly-associated intellectual disability syndrome in a Pakistani family; also identified a heterozygous deletion encompassing the NRXN1 in this family, which is present in 2 affected sibs with complex phenotype and the mother with mild phenotype PMID: 24440292
    25. These data reinforce a role for synaptic defects of NRXN1beta in neurodevelopmental disorders. PMID: 24064682
    26. The rs10187911(NRXN1 protein) on 2p16.3 was significantly associated with lung cancer development (dominant model, OR of TG or GG, 1.58, P = 0.025). PMID: 23772147
    27. based on in vitro models, NRXN1 deletions impact several biological processes during neurodevelopment, including synaptic adhesion and neuron differentiation. PMID: 23536886
    28. alpha- or beta-NRXN-1 isoforms expressed under C. elegans nrx-1 promoter rescue impairment of exploratory behavior and sinusoidal postural movement in nrx-1 C elegans mutant. PMID: 23638761
    29. study supports a pathogenic role for heterozygous exonic deletions of NRXN1 in neurodevelopmental disorders PMID: 23533028
    30. The results are consistent with the proposal that rare CNVs play a role in TS aetiology and suggest a possible role for rearrangements in the COL8A1 and NRXN1 gene regions PMID: 23533600
    31. Expression levels of neurexin and neuroligin in ENS are significantly down-regulated in HSCR, which may be involved in the pathogenesis of HSCR. PMID: 23264101
    32. Deletions in both affected and control individuals were clustered in the 5' portion of NRXN1. PMID: 23472757
    33. Patients with exonic deletions in NRXN1 manifested intellectual disability, infantile hypotonia and ASDs. PMID: 22617343
    34. In both human and mouse, NRXN1 is co-expressed with numerous cell signaling genes and known schizophrenia candidates. PMID: 22832527
    35. We conclude that exon-disrupting deletions of NRXN1 represent a genetic risk factor in the genetically complex predisposition of common idiopathic generalized epilepsies PMID: 23294455
    36. Five genes have been directly disrupted in Tourette Syndrome by independent genomic rearrangements and copy number variations with unique breakpoints. PMID: 22948383
    37. a possible gene-dose effect of NRXN1 mutations on type and severity of mental illness PMID: 22337556
    38. The data reported here support a role for synaptic defects of neurexin-1beta in neurodevelopmental disorders. PMID: 22504536
    39. This study demonistrated that there was a statistically significant association of neurexin-1 SNP P300P (rs2303298) with risk of autism in Chinese Han population. PMID: 22405623
    40. Neurexin-1alpha is a component of the beta-cell secretory machinery and contributes to secretory granule docking, most likely through interactions with granuphilin. PMID: 22235116
    41. Biallelic NRXN1 mutations result in a severe recessive mental retardation syndrome. PMID: 21964664
    42. These results suggest that the rs1045881 NRXN1 polymorphism may influence clozapine response. PMID: 21890328
    43. Presenilin/gamma-secretase regulates neurexin processing at synapses PMID: 21559374
    44. Truncating mutations in NRXN1 is associated with autism spectrum disorders and schizophrenia PMID: 21424692
    45. The mutational testing found a heterozygous deletion in NRXN1 in one patient. PMID: 21827697
    46. a neural and cognitive susceptibility mechanism by which the NRXN1 gene confers risk for both schizophrenia and autism spectrum disorders PMID: 21687627
    47. Schizophrenia patients antipsychotic response may be altered depending on the synaptic connectivity. NRXN1 deletions have also been associated with schizophrenia. observed a trend toward association of clozapine response with the rs12467557 PMID: 20860064
    48. findings suggest that NRXN1 might represent a major susceptibility gene for schizophrenia in Chinese Han population. PMID: 21477380
    49. The results of this study do not suggest the existence of rare, highly penetrant NRXN1 mutations in patients with schizophrenia. PMID: 21288692
    50. The rs6721498 and rs2193225 of NRXN1 were genotyped in 2516 Japanese with various smoking habits. PMID: 20414139

    顯示更多

    收起更多

  • 相關疾病:
    Pitt-Hopkins-like syndrome 2 (PTHSL2)
  • 亞細胞定位:
    Cell junction, synapse, presynaptic cell membrane; Single-pass type I membrane protein.
  • 蛋白家族:
    Neurexin family
  • 組織特異性:
    Brain.
  • 數據庫鏈接:

    HGNC: 8008

    OMIM: 600565

    STRING: 9606.ENSP00000385142

    UniGene: Hs.637685



主站蜘蛛池模板: 天堂中文8资源在线8| 国产亚洲欧美精品永久| 狠狠色狠狠色综合日日五| 国产成人拍精品视频午夜网站| 国产精品无码成人午夜电影| 国产美女自卫慰水免费视频| 亚洲顶级裸体av片| 日本xxx在线观看免费播放| 无码aⅴ在线观看| 欧美巨鞭大战丰满少妇| 男女性潮高清免费网站| 欧美大香线蕉线伊人久久| av小次郎收藏| 日本内射精品一区二区视频| 少妇高潮无套内谢| 免费无码又爽又刺激高潮的动态图| 69国产成人精品午夜福中文| 欧美xxxx做受性欧美88| 久99久无码精品视频免费播放| 学生妹无套内射正在播放| 亚洲综合日韩av无码毛片| 午夜福利三级理论电影| av怡红院一区二区三区| 无码中文av有码中文a| 国产欧洲精品自在自线官方| 亚洲国产成人第一天堂| 精品一区二区三区在线成人| 亚洲乱亚洲乱妇中文影视| 18禁无遮挡肉动漫在线播放观看| 男人靠女人的免费视频| 国产熟妇久久777777| 99久久精品无码一区二区毛片| 一二三四观看视频社区在线| 999久久久免费精品国产| 人妻无码久久精品| 久久精品成人无码观看不卡| 久久精品日日躁夜夜躁| 在线看片福利无码网址| 奇米精品视频一区二区三区| 亚洲精品综合一区二区三| 丰满人妻无码∧v区视频|