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SHP2 Recombinant Rabbit mAb

Cat No.: RMA02899
规格:
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  • Western blot analysis of Anti-SHP2 antibody(RMA02899) Gel: 10% SDS-PAGE Lysate: 20 μg Primary antibody: RMA02899(SHP2 antibody)at dilution 1:1000 Secondary antibody: Goat anti rabbit IgG (SPA10002)at 1:1000 dilution

Product Name: SHP2 Recombinant Rabbit mAb
Cat No.: RMA02899
Clonality: Monoclonal
Species Reactivity: Human
Tested Applications: WB, IHC, ICC/IF, FC, IP
Recommended Dilution: WB, IHC, ICC/IF, FC, IP
Size: 30ul 50ul 100uL
Format: Liquid
Source: Rabbit
Purification Method: Affinity Purification
Isotype: IgG
Conjugate: Un-conjugated
Storage: Store at -20°C. Supplied in 50nM Tris-Glycine(pH 7.4), 0.15M NaCl, 40%Glycerol, 0.01% sodium azide a
Immunogen: A synthetic peptide of human SHP2
Calculated Molecular Weight: 68 kDa
Observed Molecular Weight: 68 kDa
GenBank Accession Number: Q06124
Gene ID (NCBI): 5781
Synonyms: CFC; NS1; JMML; SHP2; BPTP3; PTP2C; METCDS; PTP-1D; SH-PTP2; SH-PTP3
Background: 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. [provided by RefSeq, Aug 2016]
Category: Primary Ab
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