ULK3 Antibody (YA2355)
(Synonyms: Serine/threonine-protein kinase ULK3; Ulk3; unc 51 like kinase 3 (C. elegans); Unc-51-like kinase 3)ULK3 Antibody (YA2355) is a Rabbit-derived and non-conjugated IgG monoclonal antibody, targeting to ULK3.
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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 50mM Tris-Glycine(pH 7.4), 0.15M NaCl, 40% Glycerol, 0.01% Sodium azide and 0.05% BSA
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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
ULK3 Antibody (YA2355) is a Rabbit-derived and non-conjugated IgG monoclonal antibody, targeting to ULK3.
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Host Rabbit
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Clonality Recombinant,Monoclonal
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Species ReactivityHuman
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Observed Molecular WeightObserved band size: 53 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: 53 kDa
A synthetic peptide of human ULK3
Endogenous
Affinity Purified
Non-conjugated
Unmodified
IgG
Product Properties
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Appearance
Solution
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Formulation
Supplied in 50mM Tris-Glycine(pH 7.4), 0.15M NaCl, 40% Glycerol, 0.01% Sodium azide and 0.05% BSA
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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.
Background
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Function
ULK3 (UNC-51-like kinase 3) is a serine/threonine protein kinase of the ULK family that functions as a regulator of Sonic Hedgehog (SHH) signaling and associated transcriptional responses mediated by GLI proteins[1][2]. Mechanistically, ULK3 possesses kinase-dependent activity, enhances GLI1 and GLI2 transcriptional function, promotes GLI nuclear translocation, and directly phosphorylates GLI proteins, placing ULK3 as an important signaling component downstream of SHH pathway activation[1][2]. In addition to Hedgehog signaling, ULK3 participates in cellular processes linked to autophagy, cellular senescence, and fibroblast activation, indicating a broader role in the coordination of stress-responsive signaling networks[2]. Disease-relevant studies further show that ULK3 contributes to cancer-associated cellular phenotypes; increased ULK3 activity has been associated with fibroblast activation and tumor-promoting functions, while ULK3 has also been identified as a determinant of keratinocyte self-renewal and tumorigenesis[2][4]. Compared with related ULK family members, ULK3 is distinguished by its strong functional connection to GLI-dependent Hedgehog signaling and by its close homology to STK36/Fused-related signaling mechanisms rather than the canonical autophagy-initiation functions commonly emphasized for ULK1 and ULK2[1][2]. Moreover, ULK3 regulates cytokinetic abscission through phosphorylation of ESCRT-III proteins, expanding its experimental relevance beyond developmental signaling and cancer biology to fundamental studies of cell division and intracellular regulation[3].
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Subcellular Localization
Cytoplasm
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Expression
Tissue_specificity:Widely expressed. Highest concentration is found in the fetal brain. In human tissues, high concentrations are found in the brain, liver, and kidneys; moderate concentrations in the testes and adrenal glands; and low concentrations in the heart, lungs, stomach, thymus, prostate, and placenta. In the brain, the hippocampus shows the highest expression, with high concentrations also detected in the cerebellum, olfactory bulb, and optic nerve. The spinal cord shows the lowest concentration in the central nervous system.
Induction:Up-regulated during senescence -
Isoforms & Post-Translational Modification
Q6PHR2 has 4 isomers: Q6PHR2-1: 53444 Da (predicted); Q6PHR2-2: 24402 Da (predicted); Q6PHR2-3: 53217 Da (predicted); Q6PHR2-4: 54997 Da (predicted).
Autophosphorylated. Autophosphorylation is blocked by interaction with SUFU -
Subunit
Interacts (via protein kinase domain) with SUFU
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SwissProt ID
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Synonyms
Serine/threonine-protein kinase ULK3; Ulk3; unc 51 like kinase 3 (C. elegans); Unc-51-like kinase 3
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Research Field
Signal Transduction
Documentation
[1]. Rabezanahary H, et al. Live virus neutralizing antibodies against pre and post Omicron strains in food and retail workers in Québec, Canada. Heliyon. 2024 May 21;10(10):e31026. [Content Brief]
[2]. Lee MJ, et al. Time to HIV rebound after infusion of long-acting broadly neutralising antibodies 3BNC117-LS and 10-1074-LS and analytical treatment interruption (the RIO trial): a double-blind, randomised, placebo-controlled trial. Lancet HIV. 2026 May 27:S2352-3018(26)00059-7. [Content Brief]
[3]. Caballe A, et al. ULK3 regulates cytokinetic abscission by phosphorylating ESCRT-III proteins. Elife. 2015 May 26;4:e06547. [Content Brief]
[4]. Kiros M, et al. Trends in HIV-1 pretreatment drug resistance and HIV-1 variant dynamics among antiretroviral therapy-naive Ethiopians from 2003 to 2018: a pooled sequence analysis. Virol J. 2023 Oct 25;20(1):243. [Content Brief]