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  4. Recombinant Mouse Peripherin-2 (Prph2), partial

Recombinant Mouse Peripherin-2 (Prph2), partial

  • 中文名稱：
    小鼠Prph2重組蛋白
  • 貨號(hào)：
    CSB-YP018775MO1
  • 規(guī)格：
  • 來源：
    Yeast
  • 其他：
  • 中文名稱：
    小鼠Prph2重組蛋白
  • 貨號(hào)：
    CSB-EP018775MO1
  • 規(guī)格：
  • 來源：
    E.coli
  • 其他：
  • 中文名稱：
    小鼠Prph2重組蛋白
  • 貨號(hào)：
    CSB-EP018775MO1-B
  • 規(guī)格：
  • 來源：
    E.coli
  • 共軛：
    Avi-tag Biotinylated

    E. coli biotin ligase (BirA) is highly specific in covalently attaching biotin to the 15 amino acid AviTag peptide. This recombinant protein was biotinylated in vivo by AviTag-BirA technology, which method is BriA catalyzes amide linkage between the biotin and the specific lysine of the AviTag.

  • 其他：
  • 中文名稱：
    小鼠Prph2重組蛋白
  • 貨號(hào)：
    CSB-BP018775MO1
  • 規(guī)格：
  • 來源：
    Baculovirus
  • 其他：
  • 中文名稱：
    小鼠Prph2重組蛋白
  • 貨號(hào)：
    CSB-MP018775MO1
  • 規(guī)格：
  • 來源：
    Mammalian cell
  • 其他：

產(chǎn)品詳情

  • 純度：
    >85% (SDS-PAGE)
  • 基因名：
    Prph2
  • Uniprot No.：
  • 別名：
    Prph2; Rds; Peripherin-2; Retinal degeneration slow protein
  • 種屬：
    Mus musculus (Mouse)
  • 蛋白長度：
    Partial
  • 蛋白標(biāo)簽：
    Tag?type?will?be?determined?during?the?manufacturing?process.
    The tag type will be determined during production process. If you have specified tag type, please tell us and we will develop the specified tag preferentially.
  • 產(chǎn)品提供形式：
    Lyophilized powder
    Note: We will preferentially ship the format that we have in stock, however, if you have any special requirement for the format, please remark your requirement when placing the order, we will prepare according to your demand.
  • 復(fù)溶：
    We recommend that this vial be briefly centrifuged prior to opening to bring the contents to the bottom. Please reconstitute protein in deionized sterile water to a concentration of 0.1-1.0 mg/mL.We recommend to add 5-50% of glycerol (final concentration) and aliquot for long-term storage at -20℃/-80℃. Our default final concentration of glycerol is 50%. Customers could use it as reference.
  • 儲(chǔ)存條件：
    Store at -20°C/-80°C upon receipt, aliquoting is necessary for mutiple use. Avoid repeated freeze-thaw cycles.
  • 保質(zhì)期：
    The shelf life is related to many factors, storage state, buffer ingredients, storage temperature and the stability of the protein itself.
    Generally, the shelf life of liquid form is 6 months at -20°C/-80°C. The shelf life of lyophilized form is 12 months at -20°C/-80°C.
  • 貨期：
    Delivery time may differ from different purchasing way or location, please kindly consult your local distributors for specific delivery time.
    Note: All of our proteins are default shipped with normal blue ice packs, if you request to ship with dry ice, please communicate with us in advance and extra fees will be charged.
  • 注意事項(xiàng)：
    Repeated freezing and thawing is not recommended. Store working aliquots at 4°C for up to one week.
  • Datasheet ：
    Please contact us to get it.

產(chǎn)品評(píng)價(jià)

靶點(diǎn)詳情

  • 功能：
    Essential for retina photoreceptor outer segment disk morphogenesis, may also play a role with ROM1 in the maintenance of outer segment disk structure. Required for the maintenance of retinal outer nuclear layer thickness. Required for the correct development and organization of the photoreceptor inner segment.
  • 基因功能參考文獻(xiàn)：
    1. ablation of Rom1 results in the conversion of an MD/PD phenotype characterized by cone functional defects and the formation of abnormal Prph2/Rom1 complexes to an RP phenotype characterized by rod-dominant functional defects and reductions in total Prph2 protein. Thus one method by which ROM1 may act as a disease modifier is by contributing to the large variability in PRPH2-associated disease phenotype PMID: 28053051
    2. quantitative FRET analysis in acutely isolated cone OS revealed that the cone degeneration-causing V268I mutation in peripherin-2 selectively reduced binding to M-opsin without affecting the peripherin-2 interaction to S-opsin or rhodopsin PMID: 27033727
    3. These results support the idea that mutations may differentially affect Prph2's role as a structural component, and its role as a functional protein key for organizing membrane domains for cellular signalling. These roles may be different in rods and cones, thus contributing to the phenotypic heterogeneity that characterizes diseases associated with Prph2 mutations. PMID: 27365499
    4. Eliminating Cngb1 and reducing RDS leads to additive defects in RDS expression levels and rod electroretinogram (ERG) function, (e.g., Cngb1-/-/rds+/- versus rds+/- or Cngb1-/-) but not to additive defects in rod ultrastructure. PMID: 26934134
    5. In the group of mice manifesting homozygous mutation in the PRPH2 gene. PMID: 27116862
    6. Our data suggest that upregulation of PRPH2 levels in combination with defects in the PRPH2 function caused by the mutation might be an important mechanism leading to cone degeneration. PMID: 26796962
    7. These data suggest that glycosylation of RDS is required for RDS function or stability in cones, a difference that may be due to extracellular versus intradiscal localization of the RDS glycan in cones versus rods. PMID: 26420485
    8. These data support a model of pattern dystrophy wherein a primary molecular defect occurring in all photoreceptors leads to secondary sequellae in adjacent tissues, an outcome which leads to macular vision loss. PMID: 25001182
    9. Peripherin-2 links CNGB1 to the light-detector rhodopsin in outer segments of rod photoreceptors. PMID: 24963162
    10. Expression of R172W mutation in cones induced subtle alterations in RDS/ROM-1 complex assembly, specifically resulting in the formation of abnormal, large molecular weight ROM-1 complexes. Fundus imaging demonstrated that R172W mice developed macular degeneration. PMID: 24463884
    11. Correcting the levels of RDS gene expression does not improve the phenotype of the rd7 model of enhanced S-cone syndrome. PMID: 23650562
    12. Structural characterization of the mechanism of RDS complex formation and the disease process underlying RDS-associated retinal degeneration. PMID: 23121719
    13. Oligomerization incompetent retinal degeneration slow is associated with mislocalization of cone opsins and cone transducin. PMID: 22183390
    14. These results suggest that while normal outer segment structure and function require RDS oligomerization, some RDS function is retained in the absence of C150. PMID: 20238000
    15. RDS does not interact with the cone CNG. PMID: 20238003
    16. These data highlight significant differences in assembly, trafficking and function of RDS in rods versus cones. PMID: 20858597
    17. Based on these findings, a relatively small fragment of the Rds promoter may be useful in future gene transfer studies to drive gene expression in photoreceptors. PMID: 20447394
    18. Two mutations at codon 244 in RDS confer different disease phenotypes: Asn244His and Asn244Lys RDS exhibit many of the abnormal biochemical hallmarks of traditional loss-of-function and gain-of-function mutations. PMID: 20055437
    19. Erythropoietin was neuroprotective to the photoreceptors in the rds mouse. PMID: 19591826
    20. Findings suggest that successful gene therapy in patients with photoreceptor defects may ultimately depend upon intervention in early stages of disease and upon accurate control of transgene expression. PMID: 11689482
    21. Although Peripherin-2 gene replacement therapy only partially restores photoreceptor morphology, it results in a 300% increase of the visual cycle protein rhodopsin, leading to retinal function improvement. PMID: 14962744
    22. R172W protein was more sensitive to tryptic digestion, indicative of a change in protein conformation, possibly contributing to the cone-dominated phenotype. PMID: 15254014
    23. We generated transgenic mice expressing P/rds with the C214S missense mutation and crossed them into rds mutant mice to elucidate the mechanism underlying the pathology of autosomal dominant retinitis pigmentosa. PMID: 15656787
    24. This study demonstrates the important role of the N-terminal portion of the peripherin (P)/rds second intradiscal (D2) loop and identifies the region between Cys165 and Asn182 as the domain for association of P/rds and its partner Rom-1. PMID: 15779916
    25. analysis of rds-peripherin in retinal organotypic culture by RNA interference PMID: 16419083
    26. This study provides novel insight into the distinct role of Rds in the OS development of rods and cones. PMID: 16585269
    27. melanoregulin regulates peripherin-2 function PMID: 17260955
    28. The R172W mutation leads to dominant cone degeneration in the mouse model, regardless of the expression level of the transgene. PMID: 18055786
    29. Histologic analysis of homozygous mutant mice at 6 weeks indicated an absence of outer segments (OS) and a 50% reduction of photoreceptor cells which progressed to complete loss of photoreceptors by 10 months. PMID: 18763016
    30. Rds C150S mutation failed to form higher-order Rds oligomers, although interactions between C150S-Rds and Rom-1 occurred in rods, but not in cones. PMID: 19050038

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  • 相關(guān)疾?。?/div>
    Responsible for retinal degeneration slow (Rds) (PubMed:8530028).
  • 亞細(xì)胞定位：
    Membrane; Multi-pass membrane protein. Cell projection, cilium, photoreceptor outer segment. Photoreceptor inner segment.
  • 蛋白家族：
    PRPH2/ROM1 family
  • 組織特異性：
    Expressed in the retina (at protein level).
  • 數(shù)據(jù)庫鏈接：


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