223

TYK2 Antibody | 7177

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SKU:
223-7177-GEN
NULL341.00 - NULL647.00

Description

TYK2 Antibody | 7177 | Gentaur UK, US & Europe Distribution

Host: Rabbit

Reactivity: Human, Mouse, Rat

Homology: N/A

Immunogen: Rabbit polyclonal TYK2 antibody was raised against a 17 amino acid peptide near the amino terminus of human TYK2.
The immunogen is located within amino acids 90 - 140 of TYK2.

Research Area: Signal Transduction

Tested Application: E, WB, IF

Application: TYK2 antibody can be used for detection of TYK2 by Western blot at 1 - 2 μg/mL. For immunofluorescence start at 20 μg/mL.
Antibody validated: Western Blot in human samples and Immunofluorescence in human samples. All other applications and species not yet tested.

Specificiy: At least three isoforms of TYK2 are known to exist; this antibody only detects the two longest isoforms.

Positive Control 1: Cat. No. 1308 - Human Small Intestine Tissue Lysate

Positive Control 2: N/A

Positive Control 3: N/A

Positive Control 4: N/A

Positive Control 5: N/A

Positive Control 6: N/A

Molecular Weight: Predicted: 131 kDa

Validation: N/A

Isoform: N/A

Purification: TYK2 Antibody is affinity chromatography purified via peptide column.

Clonality: Polyclonal

Clone: N/A

Isotype: IgG

Conjugate: Unconjugated

Physical State: Liquid

Buffer: TYK2 Antibody is supplied in PBS containing 0.02% sodium azide.

Concentration: 1 mg/mL

Storage Condition: TYK2 antibody can be stored at 4˚C for three months and -20˚C, stable for up to one year.

Alternate Name: TYK2 Antibody: JTK1, Non-receptor tyrosine-protein kinase TYK2

User Note: Optimal dilutions for each application to be determined by the researcher.

BACKGROUND: TYK2 Antibody: TYK2 is a member of the Janus kinases (JAKs) protein families. TYK2 associates with the cytoplasmic domain of type I and type II cytokine receptors and promulgate cytokine signals by phosphorylating receptor subunits and is also a component of both the type I and type III interferon signaling pathways. As such, it may play a role in anti-viral immunity. A mutation in this gene has been associated with hyperimmunoglobulin E syndrome (HIES) - a primary immunodeficiency characterized by elevated serum immunoglobulin E.

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