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

SAG Antibody, Biotin conjugated

  • 中文名稱:
    SAG兔多克隆抗體, Biotin偶聯
  • 貨號:
    CSB-PA020669YD01HU
  • 規格:
    ¥880
  • 其他:

產品詳情

  • 產品名稱:
    Rabbit anti-Homo sapiens (Human) SAG Polyclonal antibody
  • Uniprot No.:
  • 基因名:
    SAG
  • 別名:
    48 kDa protein antibody; Arrestin 1 antibody; Arrestin antibody; ARRS_HUMAN antibody; Retinal S antigen (48 KDa protein) antibody; Retinal S-antigen antibody; Rod photoreceptor arrestin antibody; RP47 antibody; S antigen antibody; S antigen retina and pineal gland (arrestin) antibody; S arrestin antibody; S-AG antibody; S-arrestin antibody; SAG antibody
  • 宿主:
    Rabbit
  • 反應種屬:
    Human
  • 免疫原:
    Recombinant Human S-arrestin protein (1-405AA)
  • 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:
    Binds to photoactivated, phosphorylated RHO and terminates RHO signaling via G-proteins by competing with G-proteins for the same binding site on RHO. May play a role in preventing light-dependent degeneration of retinal photoreceptor cells.
  • 基因功能參考文獻:
    1. This is the first dominant-acting mutation identified in SAG, a founder mutation possibly originating in Mexico several centuries ago. The phenotype is clearly adRP and is distinct from the previously reported phenotypes of recessive null mutations, that is, Oguchi disease and recessive RP. PMID: 28549094
    2. Macular dysfunction can occur in Oguchi disease with the 1147delA mutation in the SAG gene. PMID: 21447990
    3. Based on their observed affinity for arrestin-1, P-opsin and inactive P-Rh very likely affect the physiological monomer-dimer-tetramer equilibrium of arrestin-1, and should therefore be taken into account when modeling photoreceptor function. PMID: 23277586
    4. Compound heterozygosity of a nonsense R193X mutation and a heterozygous deletion of 3,224 bp encompassing exon 2 in the SAG gene is the cause of Oguchi's disease in a Chinese family. PMID: 22419846
    5. the arrestin 1147delA, which has been known as a frequent cause of Oguchi disease, also may be related to the pathogenesis of autosomal recessive RP. PMID: 21922265
    6. We describe a case of Oguchi disease with unusual findings caused by a putative heterozygous mutation in the SAG gene. PMID: 21987685
    7. maintenance of low levels of the active monomer is the biological role of arrestin-1 self-association PMID: 21288033
    8. Rhodopsin-arrestin complexes alter the morphology of endosomal compartments and severely damage receptor-mediated endocytic functions in retinitis pigmentosa. PMID: 15232620
    9. The existence of 2 novel mutations of the arrestin gene in 2 unrelated Japanese patients strongly supports the previous data that arrestin gene mutations are associated with Oguchi's disease PMID: 15234147
    10. Mutation 926delA of the SAG gene is the main cause of Oguchi disease in Japanese. This mutation appears to have been inherited from a single founder. PMID: 15295660
    11. The tetramer form of arrestin increases the arrestin-binding capacity of microtubules while readily dissociating to supply active monomer when it is needed to quench rhodopsin signaling. PMID: 17332750
    12. ARRESTIN binds to different phosphorylated regions of the thyrotropin-releasing hormone receptor with distinct functional consequences. PMID: 18413662
    13. S-Ag specific T cells are present in certain active Behcet's disease patients, and most of them are activated memory CD4(+) T cells. PMID: 18685727

    顯示更多

    收起更多

  • 相關疾病:
    Night blindness, congenital stationary, Oguchi type 1 (CSNBO1); Retinitis pigmentosa 47 (RP47)
  • 亞細胞定位:
    Cell projection, cilium, photoreceptor outer segment. Membrane; Peripheral membrane protein.
  • 蛋白家族:
    Arrestin family
  • 組織特異性:
    Detected in retina, in the proximal portion of the outer segment of rod photoreceptor cells (at protein level).
  • 數據庫鏈接:

    HGNC: 10521

    OMIM: 181031

    KEGG: hsa:6295

    STRING: 9606.ENSP00000386444

    UniGene: Hs.32721



主站蜘蛛池模板: 欧美熟妇的性裸交| 国产av熟女一区二区三区| 国精品无码人妻一区二区三区| 欧美日韩免费专区在线| 无码精品日韩专区| 伊人色合天天久久综合网| 久久丫精品久久丫| 7777精品久久久大香线蕉| 女被啪到深处喷水gif动态图| 四虎精品成人a在线观看| 图片小说视频一区二区| 人人爽人人爽人人片a| 720lu国产刺激无码| 人妻少妇精品久久| 国产成人无码专区| 精品高朝久久久久9999| 在线精品国产大象香蕉网| 欧美成人一区二免费视频软件| 亚洲gv猛男gv无码男同| 一色屋精品视频在线观看免费| 加勒比东京热无码一区| 久久精品中文字幕| 亚洲va久久久噜噜噜久久男同| 亚洲精品综合一区二区| 国模吧无码一区二区三区| 国产a国产片国产| 免费啪视频在线观看视频日本| 成人毛片18女人毛片免费| 欧美巨鞭大战丰满少妇| 亚 洲 成 人 网站在线观看| 99久久精品国产免费| 亚洲久热无码av中文字幕| 国产三级在线观看免费| 成人欧美一区二区三区a片| 人妻系列影片无码专区| 久久午夜无码鲁丝片午夜精品| 少妇的丰满3中文字幕| 男女猛烈无遮挡免费视频app | 4hu四虎永久在线观看| 华人在线亚洲欧美精品| 国产精品va在线播放|