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Phospho-FUNDC1 (Ser17) Antibody Antibodies Molecular Depot
Phospho-FUNDC1 (Ser17) Antibody Antibodies Molecular Depot
Phospho-FUNDC1 (Ser17) Antibody Antibodies Molecular Depot
Phospho-FUNDC1 (Ser17) Antibody Antibodies Molecular Depot

Phospho-FUNDC1 (Ser17) Antibody

$895.00

    Catalog Number: B2017874 (50 μL)

    Phospho-FUNDC1 (Ser17) Antibody is a 50 μL site-specific antibody that detects FUNDC1 phosphorylated at serine 17. This phospho-specific reagent is a powerful tool for studying FUNDC1-mediated mitophagy, mitochondrial quality control, and cellular responses to hypoxia or stress. Ideal for Western blotting, immunohistochemistry, and immunofluorescence in mitophagy and mitochondrial dynamics research.Custom bulk amounts of this product are available upon request.

    Products are for in vitro research use only (RUO).

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Phospho-FUNDC1 (Ser17) Antibody – Research Use Only

Phospho-FUNDC1 (Ser17) Antibody is a site-specific polyclonal antibody that recognizes FUNDC1 phosphorylated at serine 17. Supplied as a 50 µL solution (Catalog #B2017874), this antibody is a valuable research tool for studying mitophagy regulation, as phosphorylation of FUNDC1 at Ser17 modulates its interaction with LC3 and plays a key role in hypoxia-induced mitophagy and mitochondrial quality control.

Catalog number: B2017874
Lot number: Batch dependent
Expiration Date: Batch dependent
Amount: 50 μL
Molecular Weight or Concentration: 17 kDa
Supplied as: Solution
Applications: Western blotting, immunohistochemistry (IHC), immunofluorescence (IF), and studies of FUNDC1-mediated mitophagy, mitochondrial dynamics, and hypoxia response
Storage: -20°C
Keywords: Phospho-FUNDC1 (Ser17), p-FUNDC1, mitophagy
Grade: Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity >18 MΩ-cm) and are filtered through 0.22 um.

Scientific Overview

FUNDC1 is an outer mitochondrial membrane protein that acts as a receptor for selective autophagy (mitophagy). Phosphorylation at Ser17 (p-FUNDC1 Ser17) is a key regulatory modification that enhances the interaction between FUNDC1 and LC3, thereby promoting mitophagosome formation, especially under hypoxic conditions or during mitochondrial stress. This phospho-specific antibody enables researchers to detect and quantify the activated/phosphorylated form of FUNDC1, facilitating studies on mitochondrial quality control, cellular adaptation to hypoxia, and the role of mitophagy in disease states such as neurodegeneration, ischemia, and cancer.

This Phospho-FUNDC1 (Ser17) Antibody is suitable for:

  • Detection of Ser17-phosphorylated FUNDC1 by Western blot
  • Immunohistochemistry and immunofluorescence analysis of mitophagy
  • Studies of hypoxia-induced mitophagy and mitochondrial dynamics
  • Investigation of FUNDC1 regulation in metabolic stress and disease models

Usage & Handling Guidance

Store at -20 °C. Avoid repeated freeze–thaw cycles by preparing single-use aliquots. For Western blotting, typical dilutions range from 1:500 to 1:2000. For IHC/IF, optimize starting from 1:100–1:500. Centrifuge briefly before use to remove any aggregates.

  • Recommended applications: Western blot, IHC, and IF
  • Working dilution: Optimize empirically (commonly 1:500–1:2000 for WB; 1:100–1:500 for IHC/IF)
  • Stability: Stable when stored frozen; aliquot to prevent repeated freeze–thaw
  • Handling: Use in a clean environment; validate specificity with appropriate controls (e.g., phosphatase treatment)

What You Get

  • 50 μL Phospho-FUNDC1 (Ser17) Antibody solution
  • Site-specific antibody recognizing FUNDC1 phosphorylated at serine 17
  • High-purity biotechnology-grade reagent suitable for sensitive detection methods
  • Convenient volume for multiple experiments and protocol optimization
  • For research use only (RUO)

Why Researchers Choose It

  • Specific detection of the functionally important Ser17-phosphorylated form of FUNDC1
  • Essential tool for studying mitophagy, hypoxia response, and mitochondrial quality control
  • High sensitivity and low background in Western blot, IHC, and immunofluorescence
  • Reliable performance in cell biology and disease model research
  • Biotechnology-grade quality ensures reproducibility

Frequently Asked Questions (FAQ)

  • What does this antibody specifically detect?
    It recognizes FUNDC1 only when phosphorylated at serine 17 (p-FUNDC1 Ser17).
  • What is the significance of Ser17 phosphorylation on FUNDC1?
    Phosphorylation at Ser17 enhances FUNDC1 binding to LC3, promoting mitophagy under hypoxic or stress conditions.
  • What dilution should I use for Western blot?
    Start with 1:500–1:2000 and optimize for your specific sample and detection system.
  • Can this antibody be used for immunofluorescence?
    Yes. It is suitable for IF and IHC after proper optimization and validation with controls.
  • How should I store the antibody?
    Store at -20 °C and avoid repeated freeze–thaw cycles by making aliquots.
This product is for Research Use Only (RUO). It is not intended for diagnostic or therapeutic use in humans or animals.

References

  • Redlich PN, Hoeprich PD Jr, Colby CB, Grossberg SE. Antibodies that neutralize human beta interferon biologic activity recognize a linear epitope: analysis by synthetic peptide mapping. Proc Natl Acad Sci U S A. 1991 May 1;88(9):4040-4. Reference
  • Kuga T, Nozaki N, Matsushita K, Nomura F, Tomonaga T. Phosphorylation statuses at different residues of lamin B2, B1, and A/C dynamically and independently change throughout the cell cycle. Exp Cell Res. 2010 Aug 15;316(14):2301-12. Reference
  • Preuss KD, Pfreundschuh M, Fadle N, Regitz E, Raudies S, Murwaski N, Ahlgrimm M, Bittenbring J, Klotz M, Schäfer KH, Held G, Neumann F, Grass S. Hyperphosphorylation of autoantigenic targets of paraproteins is due to inactivation of PP2A. Blood. 2011 Sep 22;118(12):3340-6. Reference
  • Kobayashi K, Yamakoshi Y, Hu JC, Gomi K, Arai T, Fukae M, Krebsbach PH, Simmer JP. Splicing determines the glycosylation state of ameloblastin. J Dent Res. 2007 Oct;86(10):962-7. Reference
  • Panasyuk G, Nemazanyy I, Zhyvoloup A, Bretner M, Litchfield DW, Filonenko V, Gout IT. Nuclear export of S6K1 II is regulated by protein kinase CK2 phosphorylation at Ser-17. J Biol Chem. 2006 Oct 20;281(42):31188-201. Reference
  • Asada A, Takahashi J, Taniguchi M, Yamamoto H, Kimura T, Saito T, Hisanaga S. Neuronal expression of two isoforms of mouse Septin 5. J Neurosci Res. 2010 May 1;88(6):1309-16. Reference
  • Talasz H, Sarg B, Lindner HH. Site-specifically phosphorylated forms of H1.5 and H1.2 localized at distinct regions of the nucleus are related to different processes during the cell cycle. Chromosoma. 2009 Dec;118(6):693-709. Reference
  • Cao L, Wang Z, Zhang D, Li X, Hou C, Ren C. Phosphorylation of myosin regulatory light chain at Ser17 regulates actomyosin dissociation. Food Chem. 2021 Sep 15;356:129655. Reference
  • O’Rourke EC, Drummond RJ, Creasey AA. Binding of 125I-labeled recombinant beta interferon (IFN-beta Ser17) to human cells. Mol Cell Biol. 1984 Dec;4(12):2745-9. Reference
  • Bueren-Calabuig JA, Michel J. Impact of Ser17 Phosphorylation on the Conformational Dynamics of the Oncoprotein MDM2. Biochemistry. 2016 May 3;55(17):2500-9. Reference

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Copy of Technical Specifications

FeatureDetails
Viewing Head Siedentopf type trinocular head, inclined at 30°, Interpupillary adjustment 53mm to 75mm, graduated diopter on left eyetube (30mm I.D. eyetubes)
Eyepieces SWH10X Widefield high eyepoint eyepiece, Field No. 22, tube O.D. 30.0 mm
Nosepiece Quintuple
Quintuple LWD Planachromat Phase 10x, 20x
Condenser TC Condenser N.A. 0.30, W.D. 73.0mm
Stage180mm(X) x 245mm(Y) plain stage with replaceable glass insert with 45mm opening, Glass Stage plate insert
IlluminationKoehler without iris, with phase slider, 3W LED
WarrantyLIMITED LIFETIME WARRANTY

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