Recommended
product-img
  • Products
  • Discover MP Targets
  • Discover Research Areas
  • mProX™ Human NPBWR2 Stable Cell Line

    [CAT#: S01YF-0923-PY137]
    Product Category:
    Membrane Protein Stable Cell Lines
    Subcategory:
    GPCR Cell Lines

    Datasheet MSDS Request COA

    Certificate of Analysis Lookup
    To download a Certificate of Analysis, please enter a lot number in the search box below. Note: Certificate of Analysis not available for kit components.
    Lot Number

    Made to Order Inquiry

    Inquiry
    Host Cell Type:
    Membrane Protein Engineering:
    Fluorescent Marker:
    Resistance:
    Deliverable:

    Product Information

    Target Protein
    NPBWR2
    Target Family
    Neuropeptide B/W Family
    Target Protein Species
    Human
    Host Cell Type
    CHO-K1;HEK293
    Target Classification
    GPCR Cell Lines
    Gene ID
    Human: 2832
    UniProt ID
    Human: P48146

    Product Properties

    Biosafety Level
    Level 1
    Activity
    Yes
    Quantity
    10⁶ cells per vial
    Applications
    Neuropeptide B/W receptor 2 (NPBWR2) has been associated with the modulation of the stress axis in chickens. Research has shown that neuropeptide W (NPW) acts as an inhibitory secretagogue for GH and prolactin via the Gi protein-coupled NPBWR2. Another study provided evidence that NPW is a potent physiological corticotropin-releasing inhibitory factor in chickens, playing a core role in suppressing the activity of the stress axis. These findings highlight the importance of NPBWR2 in the endocrine system and its potential implications in stress-related disorders.

    Protocols

    Please visit our protocols page.

    Customer Reviews

    There are currently no Customer reviews or questions for mProX™ Human NPBWR2 Stable Cell Line (S01YF-0923-PY137). Click the button above to contact us or submit your feedback about this product.

    FAQ

    chat Richard (Verified Customer)

    How can NPBWR2 be studied in the context of membrane protein dynamics? Jul 15 2021

    chat Patrick Liam (Creative Biolabs Scientific Support)

    NPBWR2, like other membrane proteins, can be studied using time-resolved X-ray scattering in solution. This technique, combined with MD simulation, helps in tracking the dynamics of membrane proteins and identifying transient intermediate states. Jul 15 2021

    chat Helen (Verified Customer)

    What are the potential applications of NPBWR2 in drug delivery and therapeutic interventions? Mar 27 2020

    chat Patrick Liam (Creative Biolabs Scientific Support)

    Although specific information on NPBWR2 is limited, membrane proteins like NPBWR2 can potentially be targeted using nanodiscs. Nanodiscs are nanometer-scale vehicles used for the in vivo delivery of drugs, therapeutic lipids, and active protein complexes, providing insights into cellular signaling complexes that assemble on a membrane surface. Mar 27 2020

    Published Data

    Fig.1 Effects of chicken NPB28 on forskolin-stimulated luciferase activity of CHO cells expressing NPBWR1 or NPBWR2 of human.

    The impact of cNPB28 at various concentrations (ranging from 10^−11M to 10^−6 M) over a 6-hour period on forskolin (2μM)-induced luciferase activity in CHO cells expressing either hNPBWR1 or hNPBWR2 was assessed using a pGL3-CRE-luciferase reporter system. In contrast, the luciferase activity stimulated by forskolin remained unaffected by cNPB28/cNPW23 treatment in CHO cells transfected with the empty pcDNA3.1(+) vector, serving as a negative control (unpublished data). The data points presented here represent the mean ± SEM of three replicates (n = 3).

    Ref: Bu, Guixian, et al. "Characterization of neuropeptide B (NPB), neuropeptide W (NPW), and their receptors in chickens: evidence for NPW being a novel inhibitor of pituitary GH and prolactin secretion." Endocrinology 157.9 (2016): 3562-3576.

    Pubmed: 27399877

    DOI: 10.1210/en.2016-1141

    Research Highlights

    Yu W, et al. "Neuropeptide B (NPB) and NPB receptor 2b (NPBWR2b) in the ricefield eel ." Fish physiology and biochemistry, 2023.
    The neuropeptide B/W signaling system is an important component of diverse physiological processes, including the central regulation of neuroendocrine axes in vertebrates. This study aimed to characterize this system in the ricefield eel and examine its potential roles in regulating adenohypophysial functions. The ricefield eel genome contains npba, npbb, and npbwr2b genes, but lacks the npw, npbwr1, and npbwr2a genes. The loss of npw and npbwr1 likely occurred in the ray-finned fish while npbwr2a was lost in specific fish species. Through whole-genome duplication, the ricefield eel has duplicates of the npba and npbb genes. Npba and npbb were expressed in the brain and some peripheral tissues, while npbwr2b was expressed in the brain and other tissues such as the pituitary, gonad, heart, and eye. Immunoreactive Npbwr2b was localized in the pituitary's Lh and Fsh cells, but not in Gh or Prl cells. Npba was found to upregulate the expression of fshb and cga, but not lhb mRNA in pituitary fragments of ricefield eels cultured in vitro, suggesting a potential role in regulating reproduction. In summary, the research confirms the involvement of the NPB system in the neuroendocrine regulation of reproduction in ricefield eels.
    Pubmed: 37670169   DOI: 10.1007/s10695-023-01237-x

    Wojciechowicz T, et al. "The Effects of Neuropeptide B on Proliferation and Differentiation of Porcine ." International journal of molecular sciences, 2023.
    Neuropeptide B (NPB) has been found to play a significant role in regulating energy homeostasis and metabolism in humans and pigs through its binding and activation of NPBWR1 and NPBWR2. Previous research has demonstrated that NPB promotes adipogenesis in rat white and brown preadipocytes as well as 3T3-L1 cells. In this present study, the effects of NPB on the proliferation and differentiation of white porcine preadipocytes into mature adipocytes were examined. The presence of NPB, NPBWR1, and NPBWR2 were identified at both the mRNA and protein levels in porcine white preadipocytes. NPB was found to increase the expression of PPARgamma, C/EBPbeta, and C/EBPalpha mRNA, as well as stimulate lipid accumulation, during the differentiation process. Additionally, NPB promoted the phosphorylation of p38 kinase, but not ERK1/2, in porcine preadipocytes. The study also revealed that NPB was unable to induce C/EBPbeta expression in the presence of a p38 inhibitor, suggesting a p38-dependent mechanism in NPB-induced differentiation of porcine preadipocytes.
    Pubmed: 37047072   DOI: 10.3390/ijms24076096

    Please note: All products are "FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR CLINICAL PROCEDURES" For licensing inquiries, please contact
    Send Inquiry Send Inquiry
    Inquiry Basket
    compare

    Go to compare