pros Antibody

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Product Specs

Buffer
Preservative: 0.03% Proclin 300
Constituents: 50% Glycerol, 0.01M PBS, pH 7.4
Form
Liquid
Lead Time
Made-to-order (14-16 weeks)
Synonyms
CG17228 antibody; Homeobox protein prospero antibody; Pro antibody; PROS 1 antibody; PROS 2 antibody; proS antibody; PROS_DROME antibody; PROS1 antibody; PROS2 antibody; Prosp antibody; Voila antibody
Target Names
pros
Uniprot No.

Target Background

Function
Prospero is a homeodomain protein that plays a crucial role in regulating neuronal identity. As a transcription factor, it controls the expression of genes like *ftz*, *eve*, and *en* in specific neuroblast progeny, and modulates the transcriptional activity of other homeodomain proteins, such as Dfd. Its function is indispensable for proper neuronal differentiation, axonal outgrowth, and pathfinding in both the central and peripheral nervous systems. Moreover, Prospero collaborates with the protein Brat to ensure proper asymmetric stem cell self-renewal.
Gene References Into Functions
  1. Research has shown that the loss of Prospero hinders the suppression of SCA8-associated neurodegeneration by Spoonbill. This suggests a potential genetic interaction and functional collaboration between Prospero and Spoonbill. PMID: 28722203
  2. Prospero is essential for the differentiation of astrocytes, but not for ensheathing glia, despite their shared lineage. PMID: 26893340
  3. The RanGEF Bj1 promotes nuclear export of Prospero, facilitating neuroblast self-renewal. PMID: 25312250
  4. Transient nuclear localization of Prospero induces quiescence in neural progenitors. PMID: 25354199
  5. Studies have shown that Prospero indirectly restricts the formation of CO(2) neurons through miR-279 and directly by repressing the shared target molecules Nerfin-1 and Esg. PMID: 22049409
  6. The homeo-prospero domain plays a crucial role in regulating Prospero's nuclear localization and DNA binding specificity. PMID: 12429095
  7. The subcellular localization of Prospero is dynamic. Its carboxy terminus, including the homeodomain and Prospero domain, plays a significant role in regulating these changes. PMID: 12529405
  8. Complete nervous system development necessitates a full complement of Prospero, and gradual decreases in its levels can proportionally alter nervous system development and function. PMID: 12605454
  9. The combined expression of Prospero, Seven-up, and Elav identifies progenitor cell types during sense organ differentiation in the Drosophila antenna. PMID: 12606283
  10. Prospero is a transcription factor that controls the differentiation between color photoreceptor cell fates. PMID: 12791270
  11. Research has identified an intron region critical for Prospero twintron splicing, providing insights into the molecular mechanism of splicing regulation involving competition between different spliceosomes. PMID: 14966268
  12. The neural precursor gene *prospero* is essential for *nerfin-1* expression in the developing Drosophila central nervous system. PMID: 15617679
  13. DTRAF1 binds to Baz and acts downstream of Egr in the Mira/Pros telophase rescue pathway. PMID: 17139248
  14. The spatio-temporal expression of Prospero is precisely regulated to ensure the correct development and function of the nervous system in *Drosophila melanogaster*. PMID: 17223099
  15. Altered Prospero expression influences the age of onset of male mating behavior. PMID: 17436071
  16. In the compound eye, *prospero* is transcribed specifically in R7 photoreceptors and cone cells. PMID: 18635611
  17. Prospero is a transcription factor that is transported to the nucleus during Drosophila embryonic nervous system development. PMID: 11262236

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Database Links

KEGG: dme:Dmel_CG17228

STRING: 7227.FBpp0293146

UniGene: Dm.7116

Protein Families
Prospero homeodomain family
Subcellular Location
Nucleus. Cytoplasm, cell cortex. Cytoplasm.

Q&A

Antibody research plays a critical role in virology, immunology, and therapeutic development. Below are structured FAQs addressing key methodological and analytical challenges in academic research, informed by current studies and technical guidelines.

Advanced Research Questions

How are engineered pro-antibodies used to mitigate on-target toxicity in monoclonal therapies?

  • Innovative design:

    • Protease-activated masking: Inhibitory domains (e.g., TGF-β LAP) block antibody binding until cleaved by disease-specific proteases like MMP-2 .

    • In vitro validation: Compare binding affinity of masked vs. activated antibodies using surface plasmon resonance (SPR).

ParameterMasked AntibodyActivated Antibody
Binding affinity (KD)>100 nM2-5 nM
Toxicity in vivoReduced liver uptakeTarget-specific action

What strategies resolve contradictions between neutralizing antibody titers and clinical protection?

  • Integrated approaches:

    • Systems serology: Profile antibody Fc-mediated effector functions (ADCC, phagocytosis) alongside neutralization .

    • Longitudinal sampling: Track antibody decay rates and memory B-cell responses over 6–12 months .

  • Case study: COVID-19 convalescent plasma trials prioritized IgG titers >1:320 for therapeutic efficacy, yet some patients with lower titers still showed clinical improvement .

How do researchers optimize custom antibody production for rare epitope targets?

  • Technical workflow:

    • Epitope mapping: Use phage display libraries or cryo-EM to identify accessible regions .

    • Host selection: Immunize multiple species (e.g., rabbits, alpacas) to increase likelihood of immune recognition .

    • Affinity maturation: Employ error-prone PCR to enhance binding specificity by 10-100x .

Methodological Best Practices

  • Cohort stratification: In serosurveys, oversample high-risk subgroups (e.g., healthcare workers) to improve statistical power .

  • Antibody stability testing: Store recombinant antibodies at -80°C with 5% glycerol to prevent aggregation .

  • Data transparency: Publish raw optical density (OD) values and threshold calculations to enable cross-study comparisons .

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