Prospero (MR1A)

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DSHB Data Sheet

Catalog Fields

Product Name/ID: Prospero (MR1A)
Available to For-Profits: Yes
Alternate Antibody Name:
Gene Name: pros
Ab Isotype: MIgG1, kappa light chain
Gene Symbol:
Antibody Registry ID: AB_528440 
Uniprot ID: P29617 
RRID:  
Entrez Gene ID: 41363 
Clonality: Monoclonal
Immunogen: GST-fusion protein domain
Clone:
Immunogen Sequence: a.a. 1196-1320
Myeloma Strain:
Epitope Mapped: No
Antigen Name: Prospero protein
Epitope Location or Sequence: Epitope located in C-terminus.
Alternate Antigen Name:
Deposit Date: 11/22/2000
Antigen Molecular Weight: 165 kDa predicted; 215 kDa observed
Depositor: Doe, C.Q.
Antigen Sequence:
Depositor Institution: University of Oregon
Antigen Species: Drosophila
Depositor Notes: This antibody recognizes a transcription factor broadly expressed and conserved in vertebrate development.
Host Species: mouse
Hybridoma Cells Available (Non-Profit): Yes
Confirmed Species Reactivity: Drosophila
Additional Information: Prospero (MR1A) shows no immunoreactivity in embryos homozygous for prospero null alleles. PMID: 7588053.
Predicted Species Reactivity:  
Human Protein Atlas:  
Additional Characterization:  
Recommended Applications: Immunofluorescence, Immunohistochemistry, Western Blot
All cell products contain the antimicrobial ProClin. Click here for additional information.
These hybridomas were created by your colleagues. Please acknowledge the hybridoma contributor and the Developmental Studies Hybridoma Bank (DSHB) in the Materials and Methods of your publications. Please email the citation to us.
For your Materials & Methods section:
Prospero (MR1A) was deposited to the DSHB by Doe, C.Q. (DSHB Hybridoma Product Prospero (MR1A))
Storage and Handling Recommendations
Although many cell products are maintained at 4°C for years without loss of activity, shelf-life at 4°C is highly variable. For immediate use, short term storage at 4°C up to two weeks is recommended. For long term storage, divide the solution into volumes of no less than 20 ul for freezing at -20°C or -80°C. The small volume aliquot should provide sufficient reagent for short term use. Freeze-thaw cycles should be avoided. For concentrate or bioreactor products, an equal volume of glycerol, a cryoprotectant, may be added prior to freezing.
Usage Recommendations
The optimal Ig concentration for an application varies by species and antibody affinity. For each product, the antibody titer must be optimized for every application by the end user laboratory. A good starting concentration for immunohistochemistry (IHC), immunofluorescence (IF), and immunocytochemistry (ICC) when using mouse Ig is 2-5 ug/ml. For western blots, the recommended concentration range of mouse Ig 0.2-0.5 ug/ml. In general, rabbit antibodies demonstrate greater affinity and are used at a magnitude lower Ig concentration for initial testing. The recommended concentrations for rabbit Ig are 0.2-0.5 ug/ml (IF, IHC and ICC) and 20-50 ng/ml (WB).

22 References

  • Initial Publication
  • IF References
  • WB References
  • IHC References
  • All References
  • Initial Publication
    IF References

    A regulatory network of Drosophila germline stem cell self-renewal.
    Perrimon N
    Developmental cell 28.4 (2014 Feb 24): 459-73.

    klumpfuss distinguishes stem cells from progenitor cells during asymmetric neuroblast division.
    Lee CY
    Development (Cambridge, England) 139.15 (2012 Aug): 2670-80.

    Split ends antagonizes the Notch and potentiates the EGFR signaling pathways during Drosophila eye development.
    Rebay I
    Mechanisms of development 124.9-10 (2007 Sep-Oct): 792-806.

    Neuralized is essential for a subset of Notch pathway-dependent cell fate decisions during Drosophila eye development.
    Rubin GM
    Proceedings of the National Academy of Sciences of the United States of America 98.10 (2001 May 8): 5637-42.

    The sexual identity of adult intestinal stem cells controls organ size and plasticity.
    Miguel-Aliaga I
    Nature 530.7590 (2016 Feb 18): 344-8.

    The lipolysis pathway sustains normal and transformed stem cells in adult Drosophila.
    Hou SX
    Nature 538.7623 (2016 Oct 6): 109-113.

    Transient Scute activation via a self-stimulatory loop directs enteroendocrine cell pair specification from self-renewing intestinal stem cells.
    Xi R
    Nature cell biology 20.2 (2018 Feb): 152-161.

    Glass promotes the differentiation of neuronal and non-neuronal cell types in the Drosophila eye.
    Treisman JE
    PLoS genetics 14.1 (2018 Jan): e1007173.

    Gene expression profiles uncover individual identities of gnathal neuroblasts and serial homologies in the embryonic CNS of Drosophila.
    Technau GM
    Development (Cambridge, England) 143.8 (2016 Apr 15): 1290-301.

    Sestrin protects Drosophila midgut from mercury chloride-induced damage by inhibiting oxidative stress and stimulating intestinal regeneration.
    Wen D
    Comparative biochemistry and physiology. Toxicology & pharmacology : CBP 248. (2021 Oct): 109083.

    Buffered EGFR signaling regulated by spitz-to-argos expression ratio is a critical factor for patterning the Drosophila eye.
    Mazumder A
    PLoS genetics 19.2 (2023 Feb): e1010622.

    RK2, a glial-specific homeodomain protein required for embryonic nerve cord condensation and viability in Drosophila.
    Tomlinson A
    Development (Cambridge, England) 120.10 (1994 Oct): 2957-66.

    WB References
    IHC References

    Replication protein a links cell cycle progression and the onset of neurogenesis in Drosophila optic lobe development.
    Luo H
    The Journal of neuroscience : the official journal of the Society for Neuroscience 33.7 (2013 Feb 13): 2873-88.

    Notch signaling regulates neuroepithelial stem cell maintenance and neuroblast formation in Drosophila optic lobe development.
    Luo H
    Developmental biology 350.2 (2011 Feb 15): 414-28.

    Drosophila Hey is a target of Notch in asymmetric divisions during embryonic and larval neurogenesis.
    Delidakis C
    Development (Cambridge, England) 137.2 (2010 Jan): 191-201.

    Split ends antagonizes the Notch and potentiates the EGFR signaling pathways during Drosophila eye development.
    Rebay I
    Mechanisms of development 124.9-10 (2007 Sep-Oct): 792-806.

    Regulated nuclear export of the homeodomain transcription factor Prospero.
    Mortin MA
    Development (Cambridge, England) 128.8 (2001 Apr): 1359-67.

    Revisiting the Drosophila microchaete lineage: a novel intrinsically asymmetric cell division generates a glial cell.
    Schweisguth F
    Development (Cambridge, England) 126.16 (1999 Aug): 3573-84.

    Regulation of cell growth by Notch signaling and its differential requirement in normal vs. tumor-forming stem cells in Drosophila.
    Lu B
    Genes & development 25.24 (2011 Dec 15): 2644-58.

    The sexual identity of adult intestinal stem cells controls organ size and plasticity.
    Miguel-Aliaga I
    Nature 530.7590 (2016 Feb 18): 344-8.

    A multiplexable TALE-based binary expression system for in vivo cellular interaction studies.
    Fulga TA
    Nature communications 8.1 (2017 Nov 21): 1663.

    Non-apoptotic caspase activation preserves Drosophila intestinal progenitor cells in quiescence.
    Baena-Lopez LA
    EMBO reports 21.12 (2020 Dec 3): e48892.

    The prospero transcription factor is asymmetrically localized to the cell cortex during neuroblast mitosis in Drosophila.
    Doe CQ
    Development (Cambridge, England) 121.10 (1995 Oct): 3187-95.

    All References

    Replication protein a links cell cycle progression and the onset of neurogenesis in Drosophila optic lobe development.
    Luo H
    The Journal of neuroscience : the official journal of the Society for Neuroscience 33.7 (2013 Feb 13): 2873-88.

    Notch signaling regulates neuroepithelial stem cell maintenance and neuroblast formation in Drosophila optic lobe development.
    Luo H
    Developmental biology 350.2 (2011 Feb 15): 414-28.

    Drosophila Hey is a target of Notch in asymmetric divisions during embryonic and larval neurogenesis.
    Delidakis C
    Development (Cambridge, England) 137.2 (2010 Jan): 191-201.

    Split ends antagonizes the Notch and potentiates the EGFR signaling pathways during Drosophila eye development.
    Rebay I
    Mechanisms of development 124.9-10 (2007 Sep-Oct): 792-806.

    Regulated nuclear export of the homeodomain transcription factor Prospero.
    Mortin MA
    Development (Cambridge, England) 128.8 (2001 Apr): 1359-67.

    Revisiting the Drosophila microchaete lineage: a novel intrinsically asymmetric cell division generates a glial cell.
    Schweisguth F
    Development (Cambridge, England) 126.16 (1999 Aug): 3573-84.

    Regulation of cell growth by Notch signaling and its differential requirement in normal vs. tumor-forming stem cells in Drosophila.
    Lu B
    Genes & development 25.24 (2011 Dec 15): 2644-58.

    The sexual identity of adult intestinal stem cells controls organ size and plasticity.
    Miguel-Aliaga I
    Nature 530.7590 (2016 Feb 18): 344-8.

    A multiplexable TALE-based binary expression system for in vivo cellular interaction studies.
    Fulga TA
    Nature communications 8.1 (2017 Nov 21): 1663.

    Non-apoptotic caspase activation preserves Drosophila intestinal progenitor cells in quiescence.
    Baena-Lopez LA
    EMBO reports 21.12 (2020 Dec 3): e48892.

    The prospero transcription factor is asymmetrically localized to the cell cortex during neuroblast mitosis in Drosophila.
    Doe CQ
    Development (Cambridge, England) 121.10 (1995 Oct): 3187-95.

    A regulatory network of Drosophila germline stem cell self-renewal.
    Perrimon N
    Developmental cell 28.4 (2014 Feb 24): 459-73.

    klumpfuss distinguishes stem cells from progenitor cells during asymmetric neuroblast division.
    Lee CY
    Development (Cambridge, England) 139.15 (2012 Aug): 2670-80.

    Neuralized is essential for a subset of Notch pathway-dependent cell fate decisions during Drosophila eye development.
    Rubin GM
    Proceedings of the National Academy of Sciences of the United States of America 98.10 (2001 May 8): 5637-42.

    The lipolysis pathway sustains normal and transformed stem cells in adult Drosophila.
    Hou SX
    Nature 538.7623 (2016 Oct 6): 109-113.

    Transient Scute activation via a self-stimulatory loop directs enteroendocrine cell pair specification from self-renewing intestinal stem cells.
    Xi R
    Nature cell biology 20.2 (2018 Feb): 152-161.

    Glass promotes the differentiation of neuronal and non-neuronal cell types in the Drosophila eye.
    Treisman JE
    PLoS genetics 14.1 (2018 Jan): e1007173.

    Gene expression profiles uncover individual identities of gnathal neuroblasts and serial homologies in the embryonic CNS of Drosophila.
    Technau GM
    Development (Cambridge, England) 143.8 (2016 Apr 15): 1290-301.

    Sestrin protects Drosophila midgut from mercury chloride-induced damage by inhibiting oxidative stress and stimulating intestinal regeneration.
    Wen D
    Comparative biochemistry and physiology. Toxicology & pharmacology : CBP 248. (2021 Oct): 109083.

    Buffered EGFR signaling regulated by spitz-to-argos expression ratio is a critical factor for patterning the Drosophila eye.
    Mazumder A
    PLoS genetics 19.2 (2023 Feb): e1010622.

    RK2, a glial-specific homeodomain protein required for embryonic nerve cord condensation and viability in Drosophila.
    Tomlinson A
    Development (Cambridge, England) 120.10 (1994 Oct): 2957-66.

    Zfh1 promotes survival of a peripheral glia subtype by antagonizing a Jun N-terminal kinase-dependent apoptotic pathway.
    Garces A
    The EMBO journal 28.20 (2009 Oct 21): 3228-43.

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