PTPN11
Anti-PTPN11 Recombinant Antibody Products
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- Species Reactivity: Human, Mouse, Rat
- Type: Rabbit IgG
- Application: WB, IP
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- Species Reactivity: Human
- Type: Rabbit IgG
- Application: WB, IF, IHC, IP
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- Species Reactivity: Human, Mouse, Rat
- Type: Rabbit IgG
- Application: IF, IHC, FC
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- Derivation: Rabbit
- Species Reactivity: Human
- Type: Rabbit IgG
- Application: WB, ICC, IF, IHC, IP
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- Species Reactivity: Human
- Type: Rabbit IgG
- Application: WB, IHC-P, IP
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- Species Reactivity: Human
- Type: Mouse IgG1
- Application: ELISA, WB
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- Species Reactivity: Human, Mouse
- Type: Rabbit IgG
- Application: WB, ICC, IF, IP
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- Target: PTPN11
- Target Species: Human
- Application: IP, Protein Purification
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- Species Reactivity: Human, Mouse
- Type: Rabbit IgG
- Application: WB, IF, IP
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- Species Reactivity: Human
- Type: Rabbit IgG
- Application: ELISA, WB, IP
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- Species Reactivity: Human
- Type: Rabbit IgG
- Application: ELISA, WB, IHC
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- Species Reactivity: Human
- Type: Rabbit IgG
- Application: ELISA, WB
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- Derivation: Mouse
- Species Reactivity: Human
- Type: Mouse IgG1
- Application: WB, IHC, ICC, FC, ELISA
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- Type: Mouse IgG2b
- Application: IHC, ICC, FC
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- Derivation: Mouse
- Species Reactivity: Human
- Type: Mouse IgG1
- Application: ELISA, FC, ICC, IF, IHC, WB
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- Species Reactivity: Human, Rat
- Type: Chicken antibody
- Application: WB
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- Derivation: Phage display library screening
- Species Reactivity: Human
- Type: IgG
- Application: WB
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For Research Use Only. Not For Clinical Use.
The protein encoded by this gene is a member of the protein tyrosine phosphatase (PTP) family. PTPs are known to be signaling molecules that regulate a variety of cellular processes including cell growth, differentiation, mitotic cycle, and oncogenic transformation. This PTP contains two tandem Src homology-2 domains, which function as phospho-tyrosine binding domains and mediate the interaction of this PTP with its substrates. This PTP is widely expressed in most tissues and plays a regulatory role in various cell signaling events that are important for a diversity of cell functions, such as mitogenic activation, metabolic control, transcription regulation, and cell migration. Mutations in this gene are a cause of Noonan syndrome as well as acute myeloid leukemia.