Product Name
Phospho-JAK2 (Y1007 + Y1008) Recombinant Rabbit Monoclonal Antibody [SY24-03] - BSA and Azide free
Antibody Type
Recombinant Rabbit monoclonal Antibody
Immunogen
Synthetic phospho-peptide corresponding to residues surrounding Tyr1007 and 1008 of human JAK2.
Target Molecular Weight
Predicted band size: 131 kDa
Positive Control
HeLa treated with 1mM sodium orthovanadate for 30 minutes cell lysate.
Storage Instructions
Store at 2-8℃. Avoid freeze.
Purification Method
Protein A affinity purified.
Function
JAK2 (Janus Kinase 2) belongs to the emerging family of non-receptor Janus tyrosine kinases, which regulate a spectrum of cellular functions downstream of activated cytokine receptors in the lympho-hematopoietic system. Immuno-logical stimuli, such as interferons and cytokines, induce recruitment of Stat transcription factors to cytokine receptor-associated JAK2. JAK2 then phosphorylates proximal Stat factors, which subsequently dimerize, translocate to the nucleus and bind to cis elements upstream of target gene promoters to regulate transcription. The canonical JAK-Stat pathway is integral to maintaining a normal immune system by stimulating proliferation, differentiation, survival, and host resistance to pathogens. Altering JAK-Stat signaling to reduce cytokine induced pro-inflammatory responses represents an attractive target for anti-inflammatory therapies. Within the JAK2 kinase domain, there is a region that has considerable sequence homology to the regulatory region of the insulin receptor. Among a variety of sites, Tyrosines 1007 and 1008 are sites of trans- or autophosphorylation in vivo and in in vitro kinase reactions.
Background References
1. Ruiz PA & Jarai G Discoidin domain receptors regulate the migration of primary human lung fibroblasts through collagen matrices. Fibrogenesis Tissue Repair 5:3 (2012).
2. Ruiz PA & Jarai G Collagen I Induces Discoidin Domain Receptor (DDR) 1 Expression through DDR2 and a JAK2-ERK1/2-mediated Mechanism in Primary Human Lung Fibroblasts. J Biol Chem 286:12912-23 (2011).
Sequence Similarity
Belongs to the protein kinase superfamily. Tyr protein kinase family. JAK subfamily.
Tissue Specificity
Ubiquitously expressed throughout most tissues.
Post-translational Modification
Autophosphorylated, leading to regulate its activity. Leptin promotes phosphorylation on tyrosine residues, including phosphorylation on Tyr-813 (By similarity). Autophosphorylation on Tyr-119 in response to EPO down-regulates its kinase activity (By similarity). Autophosphorylation on Tyr-868, Tyr-966 and Tyr-972 in response to growth hormone (GH) are required for maximal kinase activity (By similarity). Also phosphorylated by TEC (By similarity). Phosphorylated on tyrosine residues in response to interferon gamma signaling. Phosphorylated on tyrosine residues in response to a signaling cascade that is activated by increased cellular retinol.
Subcellular Location
Nucleus, Endomembrane system, Cytoplasm.
Synonyms
JAK 2 antibody
JAK-2 antibody
JAK2 antibody
JAK2_HUMAN antibody
Janus Activating Kinase 2 antibody
Janus kinase 2 (a protein tyrosine kinase) antibody
Janus kinase 2 antibody
JTK 10 antibody
JTK10 antibody
kinase Jak2 antibody
Expand
JAK 2 antibody
JAK-2 antibody
JAK2 antibody
JAK2_HUMAN antibody
Janus Activating Kinase 2 antibody
Janus kinase 2 (a protein tyrosine kinase) antibody
Janus kinase 2 antibody
JTK 10 antibody
JTK10 antibody
kinase Jak2 antibody
OTTHUMP00000043260 antibody
THCYT3 antibody
Tyrosine protein kinase JAK2 antibody
Tyrosine-protein kinase JAK2 antibody
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☑ Cell treatment (CT)
This data was developed using ET1607-34, the same antibody clone in a different buffer formulation.
Western blot analysis of Phospho-JAK2 (Y1007 + Y1008) on different lysates with Rabbit anti-Phospho-JAK2 (Y1007 + Y1008) antibody (ET1607-34) at 1/1,000 dilution.
Lane 1: HeLa cell lysate
Lane 2: HeLa treated with 1mM sodium orthovanadate for 30 minutes cell lysate
Lysates/proteins at 20 µg/Lane.
Predicted band size: 131 kDa
Observed band size: 120 kDa
Exposure time: 3 minute; ECL: K1801;
4-20% SDS-PAGE gel.
Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (ET1607-34) at 1/1,000 dilution was used in 5% NFDM/TBST at 4℃ overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1/50,000 dilution was used for 1 hour at room temperature.
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This data was developed using ET1607-34, the same antibody clone in a different buffer formulation.
ICC staining of Phospho-JAK2 (Y1007 + Y1008) in Hela cells (green). Formalin fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 10 minutes at room temperature and blocked with 1% Blocker BSA for 15 minutes at room temperature. Cells were probed with the primary antibody (ET1607-34, 1/50) for 1 hour at room temperature, washed with PBS. Alexa Fluor®488 Goat anti-Rabbit IgG was used as the secondary antibody at 1/1,000 dilution. The nuclear counter stain is DAPI (blue).
Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"