Tyk 2 Antibody (YA5094)
(Synonyms: TYK2; Non-receptor tyrosine-protein kinase TYK2)Tyk 2 Antibody (YA5094) is a Rabbit-derived and non-conjugated monoclonal antibody, targeting to Tyk 2.
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Host:
Rabbit
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Isotype:
IgG
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Application:
WB, IHC-P
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Reactivity :
Human
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Formulation:
Supplied in PBS (pH7.4), 0.1% BSA, 40% Glycerol, 0.2% Proclin950.
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Conjugation:
Non-conjugated
Applications
| Application |
WB
WB: Western Blot
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IHC-P
IHC-P: Immunohistochemistry-Paraffin
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|---|---|---|
| Dilution Ratio | 1:5000-6000 | 1:200-1000 |
Product Details
Tyk 2 Antibody (YA5094) is a Rabbit-derived and non-conjugated monoclonal antibody, targeting to Tyk 2.
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Host Rabbit
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Clonality Recombinant
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Species ReactivityHuman
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Calculated Molecular Weight Predicted band size: 134 kDa;
Purified recombinant fragment(aa 832-1187) of Tyk 2 expressed in E. Coli.
Endogenous
affinity purified.
Non-conjugated
Unmodified
IgG
Product Properties
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Appearance
Solution
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Formulation
Supplied in PBS (pH7.4), 0.1% BSA, 40% Glycerol, 0.2% Proclin950.
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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
Tyrosine kinase 2 (TYK2) is a non-receptor Janus kinase (JAK) family member essential for cytokine signaling in immune cells[1][2]. Mechanistically, TYK2 mediates signal transduction downstream of interleukin-12 (IL-12), interleukin-23 (IL-23), type I interferons (IFN-α/β), and the IL-10 cytokine family, activating STAT transcription factors and regulating T helper cell differentiation[1][2][3]. Compared with other JAK isoforms, TYK2 exhibits distinct pseudokinase (JH2) and kinase (JH1) domains, enabling selective allosteric modulation without broadly inhibiting JAK1-3[4][2]. Loss-of-function or kinase-inactive mutations in TYK2 lead to impaired IFN and IL-12 signaling, resulting in immune deficiencies and altered antiviral responses in murine and human models[5][6]. In disease contexts, TYK2 is implicated in autoimmune disorders, including psoriasis, inflammatory bowel disease, and systemic lupus erythematosus, via dysregulated IL-23/TH17 and type I interferon pathways[7][8][2][3]. Selective inhibitors targeting the TYK2 JH2 pseudokinase domain, such as deucravacitinib or TAK-279, suppress pathogenic cytokine signaling with high specificity, preserving other JAK-mediated functions and providing therapeutic benefits in preclinical and clinical studies[4][7][2][3]. Experimental applications exploit TYK2-selective inhibition to dissect cytokine-driven immune responses and validate downstream transcriptional and phenotypic effects in immune cell models[9][3]. These compounds demonstrate potent modulation of human T cells, primary immune cells, and murine models of colitis or psoriasis, highlighting their translational relevance[4][7][2].
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Expression
Tissue_specificity:Observed in all cell lines analyzed. Expressed in a variety of lymphoid and non-lymphoid cell lines -
Subunit
Interacts (via FERM domain) with JAKMIP1 (PubMed:15277531, PubMed:20478313). Interacts with PIK3R1; this interaction is important for cell migration (PubMed:10995743). Interacts with MPL/TPOR (PubMed:15899890)
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SwissProt ID
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Synonyms
TYK2; Non-receptor tyrosine-protein kinase TYK2
Documentation
[1]. Zhou Y, et al. Novel Small Molecule Tyrosine Kinase 2 Pseudokinase Ligands Block Cytokine-Induced TYK2-Mediated Signaling Pathways. Front Immunol. 2022 May 20;13:884399. [Content Brief]
[2]. Karjalainen A, et al. Cell-type-specific requirement for TYK2 in murine immune cells under steady state and challenged conditions. Cell Mol Life Sci. 2025 Mar 2;82(1):98. [Content Brief]
[4]. Strobl B, et al. Tyrosine kinase 2 (TYK2) in cytokine signalling and host immunity. Front Biosci (Landmark Ed). 2011 Jun 1;16(9):3214-32. [Content Brief]
[5]. Wöss K, et al. TYK2: An Upstream Kinase of STATs in Cancer. Cancers (Basel). 2019 Nov 5;11(11):1728. [Content Brief]
[6]. Schlapbach C, et al. TYK-ing all the boxes in psoriasis. J Allergy Clin Immunol. 2022 Jun;149(6):1936-1939. [Content Brief]
[7]. Prchal-Murphy M, et al. TYK2 kinase activity is required for functional type I interferon responses in vivo. PLoS One. 2012;7(6):e39141. [Content Brief]
[8]. Rane SS, et al. Characterising a Novel Therapeutic Target for Psoriasis, TYK2, Using Functional Genomics. Int J Mol Sci. 2024 Dec 9;25(23):13229. [Content Brief]
[9]. He X, et al. Selective Tyk2 inhibitors as potential therapeutic agents: a patent review (2015-2018). Expert Opin Ther Pat. 2019 Feb;29(2):137-149. [Content Brief]