Your Good Partner in Biology Research

  1. 首頁
  2. 蛋白
  3. 重組蛋白
  4. Recombinant Drosophila melanogaster Protein decapentaplegic (dpp)

Recombinant Drosophila melanogaster Protein decapentaplegic (dpp)

  • 中文名稱：
    黑腹果蠅dpp重組蛋白
  • 貨號：
    CSB-YP357184DLU
  • 規(guī)格：
  • 來源：
    Yeast
  • 其他：
  • 中文名稱：
    黑腹果蠅dpp重組蛋白
  • 貨號：
    CSB-EP357184DLU
  • 規(guī)格：
  • 來源：
    E.coli
  • 其他：
  • 中文名稱：
    黑腹果蠅dpp重組蛋白
  • 貨號：
    CSB-EP357184DLU-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：
    黑腹果蠅dpp重組蛋白
  • 貨號：
    CSB-BP357184DLU
  • 規(guī)格：
  • 來源：
    Baculovirus
  • 其他：
  • 中文名稱：
    黑腹果蠅dpp重組蛋白
  • 貨號：
    CSB-MP357184DLU
  • 規(guī)格：
  • 來源：
    Mammalian cell
  • 其他：

產(chǎn)品詳情

  • 純度：
    >85% (SDS-PAGE)
  • 基因名：
    dpp
  • Uniprot No.：
  • 別名：
    dpp; CG9885Protein decapentaplegic; Protein DPP-C
  • 種屬：
    Drosophila melanogaster (Fruit fly)
  • 蛋白長度：
    Full Length of Mature Protein
  • 表達區(qū)域：
    457-588
  • 氨基酸序列
    DVSG GEGGGKGGRN KRQPRRPTRR KNHDDTCRRH SLYVDFSDVG WDDWIVAPLG YDAYYCHGKC PFPLADHFNS TNHAVVQTLV NNMNPGKVPK ACCVPTQLDS VAMLYLNDQS TVVLKNYQEM TVVGCGCR
  • 蛋白標簽：
    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：
    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)品評價

靶點詳情

  • 功能：
    Required during oogenesis for eggshell patterning and dorsal/ventral patterning of the embryo. Acts as a morphogen during embryogenesis to pattern the dorsal/ventral axis, specifying dorsal ectoderm and amnioserosa cell fate within the dorsal half of the embryo; this activity is antagonized by binding to sog and tsg. Induces the formation of visceral mesoderm and the heart in early embryos. Required later in embryogenesis for dorsal closure and patterning of the hindgut. Also functions postembryonically as a long-range morphogen during imaginal disk development; is responsible for the progression of the morphogenetic furrow during eye development. Patterns the wing imaginal disk along its anterior/posterior axis and has a role in positioning pro-veins. Also required to subdivide the wing disk along the proximal/distal axis into body wall (notum) and wing. Ensures the correct architecture of wing epithelial cells. Has multiple roles in the developing tracheal system, controlling directed tracheal cell migration during embryogenesis and later specifying the fate of fusion cells in the tracheal branches. Required for viability of larvae. Essential for the maintenance and division of germline stem cells in the ovary. Signals via the type I receptor tkv, the type II receptor punt, and in some tissues via the type I receptor sax, in a signaling cascade that leads to activation and repression of target genes.
  • 基因功能參考文獻：
    1. analysis of phenotype caused by misexpression of Wg, a negative regulator of eye development, using GMR17E04-Gal4, GMR18D08-Gal4 with existing dpp-Gal4 driver, which suggests the need for revisiting misexpression studies with Gal4 drivers PMID: 29702674
    2. Loss of Pngl results in a severe decrease in the level of Dpp homodimers and abolishes BMP autoregulation in the visceral mesoderm mediated by Dpp and Tkv homodimers. Loss of Pngl results in developmental midgut defects reminiscent of midgut-specific loss of BMP signaling. PMID: 28826503
    3. The authors find that both arms of the TFGb signaling pathways specifically instruct the pale photoreceptor subset in R8. The Activin arm utilizes the three ligands dActb, Daw, and Myo non-redundantly to activate Babo and downstream dSmad2 in R8, while the BMP arm signals by way of Dpp and Gbb to Tkv and Mad. PMID: 28853393
    4. Dpp regulates growth and proliferation rates equally in central and lateral regions of the developing wing appendage and reduced levels of Dpp affects similarly the width and length of the resulting wing. PMID: 28675372
    5. Here, by removing dpp from the stripe at different time points, the authors show that the dpp stripe source is indeed required for wing disc growth, also during third instar larval stages. PMID: 28675373
    6. With two independent conditional alleles of dpp, the authors find that the stripe of Dpp is essential for wing growth. The authors then show that this requirement, but not patterning, can be fulfilled by uniform, low level, Dpp expression. Thus, the stripe of Dpp ensures that signalling remains above a pro-growth threshold, while at the same time generating a gradient that patterns cell fates. PMID: 28675374
    7. Study provide evidence of yet another mechanism by which Dpp regulates the expression of its target retinal retinal determining (RD) genes independent of its bona fide transcriptional regulator specifically during induction of ectopic eyes. Apart from previously known transcriptional activation of the RD genes, Dpp simultaneously triggers another signaling cascade that involves dTak1-mediated activation of JNK. PMID: 27270790
    8. we found that the Dpp target gene sal is only expressed in peripodial epithelium (DP, also known as pseudostratified columnar epithelia) , not in PE cells, also known as squamous epithelia, although pMad is present in the PE. PMID: 27452716
    9. Here we provide evidence that although wild type CtBP negatively and dominantly influences Dpp signaling in fly presumptive wings, mutant CtBP unable to form dimer does not, indicating that dimerization is required for the repression role of CtBP in Dpp signaling in vivo. PMID: 29225171
    10. Dpp activates signaling cascade involving dTak1 and JNK, to induce ectopic Mmp1 expression. PMID: 28696218
    11. ECM over planar cell polarity mutant cells had reduced levels of laminin, Dally and Dlp, and whereas Dpp-receiving ASP cytonemes navigated in the Dally layer and required Dally (but not Dlp), FGF-receiving ASP cytonemes navigated in the Dlp layer, requiring Dlp (but not Dally). PMID: 27591355
    12. The authors show that Pent internalises the Dpp co-receptors, the glypicans Dally and Dally-like protein (Dlp), and propose that this internalisation is important in the establishment of a long range Dpp gradient. PMID: 27269283
    13. The expression of optix is activated by Dpp and repressed by the Spalt proteins, becoming restricted to the most anterior region of the wing blade. PMID: 28760811
    14. En forms a complex with Nejire (Nej), the Drosophila ortholog of histone acetyltransferase CBP/p300, and directs Nej to this cis-regulatory region where Nej functions as the co-activator for dpp expression. PMID: 28928281
    15. Basement membrane elimination, in contrast, attenuated signaling by bone morphogenetic protein/transforming growth factor beta ligand Dpp, which was not efficiently retained within the tissue and escaped to the body cavity. PMID: 28697337
    16. This report provides a genetic analysis of primary nociceptive neuron mechanisms that promote sensitization in response to injury. Drosophila melanogaster larvae whose primary nociceptive neurons were reduced in levels of specific components of the BMP signaling pathway, were injured and then tested for nocifensive responses to a normally subnoxious stimulus. PMID: 28855331
    17. Dad and Dpp activity is dynamically regulated in the adult Drosophila middle midgut. PMID: 27570230
    18. Here we uncover a cell non-autonomous requirement for the Epidermal growth factor receptor (Egfr) pathway in the lateral epidermis for sustained dpp expression in the LE. Specifically, we demonstrate that Egfr pathway activity in the lateral epidermis prevents expression of the gene scarface (scaf), encoding a secreted antagonist of JNK signaling PMID: 28628612
    19. In this work, we have explored the disc autonomous function of TGFbeta that promotes wing imaginal disc growth. We have studied the genetic interactions between TGFbeta signaling and other pathways regulating wing disc growth, such as the Insulin and Hippo/Salvador/Warts pathways, as well as cell cycle regulators. PMID: 28315837
    20. During normal development, Dpp represses hth and tsh ensuring that the progenitor state is transient. However, cells in which Hth+Tsh expression is forcibly maintained use Dpp to enhance their proliferation. PMID: 27502436
    21. Here we demonstrate that each prostate-like secondary cell (SC) in the paired adult Drosophila melanogaster male accessory glands contains approximately ten large DCGs, which are loaded with the Bone Morphogenetic Protein (BMP) ligand Decapentaplegic (Dpp). PMID: 27727275
    22. disruption of dpp expression causes apoptosis in peripodial cells and underlying disc proper cells PMID: 26500262
    23. we elucidate the genetic network elicited by Snoo and Dpp activity. These results illustrate a regulatory mechanism that translates intrinsic potential and extrinsic cues into the facultative stem cell features of differentiated progenitors. PMID: 26942411
    24. During oogenesis lgd loss of function causes ectopic activation of the Drosophila BMP signalling pathway. PMID: 25804739
    25. in the absence of Dpp spreading, wing disc patterning is lost; however, lateral cells still divide at normal rates PMID: 26550827
    26. Cullin-2 protein present in the somatic cells is involved in a non cell-autonomous regulation of the extent of Dpp signaling and thus controls the differentiation of GSCs to cystoblasts PMID: 26206612
    27. Dpp and Gbb are produced by enterocytes and act in conjunction to promote intestinal stem cell self-renewal by antagonizing Notch signaling. PMID: 24618900
    28. Mad linker phosphorylations control the intensity and range of the BMP-activity gradient in developing Drosophila tissues. PMID: 25377173
    29. Thickveins (Tkv; a type I receptor of Dpp) is highly expressed in stromal cells next to Dpp-producing cells and functions to remove excess Dpp outside the stem cell niche. PMID: 26008746
    30. Authors studied BMP-dependent gene regulation during Drosophila oogenesis by following the signal transmission from Dpp to its target broad (br), a gene with a crucial function in eggshell patterning and identified regulatory sequences that account for expression of both brk and br, and connect these to the transcription factors of the pathway. PMID: 25704512
    31. Dpp/Gbb signaling is required for normal intestinal regeneration during infection. PMID: 25553980
    32. Decapentaplegic (DPP) and JNK form a coherent feed-forward loop that controls the specification and differentiation of leading edge cells during Drosophila melanogaster dorsal closure. PMID: 25601405
    33. Dpp plays a dual role during dorsal closure. It cooperates with JNK in stimulating cell migration and also prevents JNK from inducing apoptosis. PMID: 25307481
    34. novel mechanisms by which Dpp affects the cellular differentiation of wing-veins. PMID: 24591046
    35. Loss of Bar from the undifferentiated retinal precursor cells leads to ectopic expression of Prospero and dPax2, two transcription factors essential for cone cell specification, resulting in excess cone cell differentiation. PMID: 24505414
    36. The signaling dynamics of the morphogen Dpp, one of several Drosophila factors controlling morphogenetic growth, was measured in the developing eye. PMID: 24757005
    37. These data reveal novel mechanisms by which post-translational regulation of Scw can modulate Dpp signaling activity. PMID: 24560644
    38. We propose that developmental BMP signaling potentiates NMJs for rapid activity-dependent structural plasticity that is achieved by muscle release of retrograde signals that regulate local presynaptic actin cytoskeletal dynamics. PMID: 24647957
    39. Genetic loss-of-function conditions for diaphanous, shibire, neuroglian, and capricious perturbed cytonemes by reducing their number or only the synapses they make with cells they target, and reduced cytoneme-mediated transport of Dpp and Dpp signaling. PMID: 24385607
    40. Drosophila piwi mutants exhibit germline stem cell tumors that are sustained by elevated Dpp signaling. PMID: 23891114
    41. Dpp signaling is required for copper cell regeneration and gut compartmentalization. PMID: 23810561
    42. optix functions together with hh to regulate dpp in the morphogenetic furrow, serving as a link between the RD network and the patterning pathways controlling normal retinal development PMID: 23792115
    43. spatial distribution of Dpp is tightly regulated at the extracellular level allowing diffusible ligands to form elaborate wing vein patterns PMID: 22542596
    44. Dpp-induced Egfr signaling triggers postembryonic wing development in Drosophila. PMID: 23479629
    45. data demonstrate Dpp signaling is primarily activated in enterocytes and Dpp is expressed specifically in tracheal cells that reach the intestinal cells through the visceral muscles PMID: 23369712
    46. We propose that the double role of KAY-alpha in the two transcriptional loops controlling Drosophila circadian behavior brings precision and stability to their oscillations PMID: 23175847
    47. Dpp transport occurs by simple, rapid diffusion in the extracellular space. PMID: 22445299
    48. dpp controls morphogenesis of the ventral adult head through expression in the eye-antennal disc by a 3.5 kb enhancer in the 5' end of the gene. We recovered a 15 bp deletion mutation within this enhancer that identified a homeotic response element. PMID: 22824425
    49. collagen IV functions to immobilize free Dpp in the Drosophila embryo PMID: 22733779
    50. Fat facets deubiquitylation of Medea/Smad4 modulates interpretation of a Dpp morphogen gradient PMID: 22745309

    顯示更多

    收起更多

  • 亞細胞定位：
    Secreted. Note=Is internalized by receptor-mediated endocytosis.
  • 蛋白家族：
    TGF-beta family
  • 組織特異性：
    Expressed in the dorsal region of the embryo, and becomes enriched in a dorsal midline stripe just prior to gastrulation. Expressed in midgut mesoderm and in two overlapping regions of the embryonic large intestine. Expressed in a long-range concentration
  • 數(shù)據(jù)庫鏈接：

    KEGG: dme:Dmel_CG9885

    STRING: 7227.FBpp0077451

    UniGene: Dm.4767