SPOP Antibody (YA2054)(PBS only)
(Synonyms: Speckle-type POZ protein; HIB homolog 1; Roadkill homolog 1)SPOP Antibody (YA2054) is a Rabbit-derived and non-conjugated IgG monoclonal antibody, targeting to SPOP.
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Host:
Rabbit
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Isotype:
IgG
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Application:
WB
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Reactivity :
Human
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Formulation:
Supplied in PBS, pH 7.4.
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Conjugation:
Non-conjugated
Applications
| Application |
WB
WB: Western Blot
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|---|---|
| Dilution Ratio | 1:500-1:1000 |
Product Details
SPOP Antibody (YA2054) is a Rabbit-derived and non-conjugated IgG monoclonal antibody, targeting to SPOP.
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Host Rabbit
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Species ReactivityHuman
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Observed Molecular WeightObserved band size: 42 kDaNote: Due to possible protein modifications or aggregation, the molecular weight should be confirmed by actual measurement, and the predicted value is for reference only.
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Calculated Molecular Weight Predicted band size: 42 kDa
A synthetic peptide of human SPOP aa129-143.
Affinity Purified
Non-conjugated
IgG
Product Properties
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Appearance
Solution
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Formulation
Supplied in PBS, pH 7.4.
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Storage & Stability
Stored at -20°C for 1 year. Avoid repeated freeze / thaw cycles.
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Shipping
Shipping with blue ice.
Verification Images
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Western blot analysis was performed on extracts from MCF-7 (lane 1, 15 μg), PC-3 (lane 2, 15 μg), and K562 (lane 3, 15 μg) using SPOP Rabbit mAb.Proteins were transferred to a PVDF membrane and blocked with 5% non-fat milk in TBST at 4°C overnight.The primary antibody (1:1000 dilution) and the loading control antibody (GAPDH, HY-P80137, 1:20000 dilution) were incubated in 5% non-fat milk in TBST for 1 hour at 37°C.Goat Anti-Rabbit IgG-HRP Secondary Antibody (1:20000 dilution) was then applied for 40 minutes at 37°C.
Background
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Function
Speckle-type POZ protein (SPOP) functions as an E3 ubiquitin ligase adaptor that mediates substrate-specific ubiquitination and proteasomal degradation[1]. Mechanistically, SPOP targets proteins such as FADD and GLI3, regulating NF-κB and Sonic hedgehog (SHH) signaling pathways, respectively, which influence cancer cell proliferation and migration[2][3]. In hepatoblastoma, SPOP acts as a tumor suppressor by modulating SLC7A1 stability and arginine metabolism through the PI3K/Akt pathway[4]. The MATH domain of SPOP is critical for recognizing diverse substrates, facilitating the orchestration of multiple cellular processes and maintaining protein homeostasis[1]. Compared with related isoforms or mutants, SPOP exhibits substrate specificity that determines differential signaling outcomes in various disease contexts[2][3]. Small molecules targeting post-translational modification (PTM) isoforms of SPOP and other ubiquitin ligases provide opportunities for isoform-selective modulation and precision therapeutic design[5]. In experimental applications, SPOP overexpression reduces tumor growth, induces apoptosis, and modulates immune signaling, highlighting its utility as a functional biomarker and therapeutic target in cancer research[6]. These findings collectively emphasize the biological relevance of SPOP in regulating protein degradation, isoform-specific pathway modulation, and its potential exploitation in experimental and therapeutic strategies[2][4][6][1][3][5].
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Subcellular Localization
Nucleus; Nucleus speckle; Cytoplasm
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Expression
Tissue_specificity:Widely expressed -
Subunit
Interacts with GLI2 and GLI3 (By similarity). Homodimer and homooligomer. Heterodimer with SPOPL. Each dimer interacts with two CUL3 molecules. Part of cullin-RING-based BCR (BTB-CUL3-RBX1) E3 ubiquitin-protein ligase complexes that contain CUL3 and homodimeric SPOP, or the heterodimer formed by SPOP and SPOPL, plus a target protein, such as MACROH2A1, PDX1/IPF1, BMI1, BRMS1 and DAXX. Interacts with IRF1; this interaction mediates IRF1 proteasomal degradation (PubMed:37622993). Interacts with HNF1A (PubMed:38018242)
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SwissProt ID
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Synonyms
Speckle-type POZ protein; HIB homolog 1; Roadkill homolog 1
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Research Field
Epigenetics and Nuclear Signaling
Documentation
References
[1]. Niu Y, et al. SPOP enhances FADD degradation and decreases the activeness of the NF-κB signaling pathway in prostate cancer: an in vitro study. Transl Androl Urol. 2024 Dec 31;13(12):2787-2800. [Content Brief]
[2]. He W, et al. S119N Mutation of the E3 Ubiquitin Ligase SPOP Suppresses SLC7A1 Degradation to Regulate Hepatoblastoma Progression. Mol Ther Oncolytics. 2020 Oct 4;19:149-162. [Content Brief]
[3]. Wang Y, et al. Integrative Multi-Omics Analysis and Experimental Validation Identify SPOP as a Prognostic Biomarker and Immune Regulator in Lung Adenocarcinoma. J Cancer. 2025 Jun 23;16(9):2984-2996. [Content Brief]
[4]. Diop A, et al. Biophysical Characterization of the Binding Mechanism between the MATH Domain of SPOP and Its Physiological Partners. Int J Mol Sci. 2023 Jun 14;24(12):10138. [Content Brief]
[5]. Burleson M, et al. GLI3 Is Stabilized by SPOP Mutations and Promotes Castration Resistance via Functional Cooperation with Androgen Receptor in Prostate Cancer. Mol Cancer Res. 2022 Jan;20(1):62-76. [Content Brief]
[6]. Meng F, et al. Drug design targeting active posttranslational modification protein isoforms. Med Res Rev. 2021 May;41(3):1701-1750. [Content Brief]