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Anti-SHP2 Rabbit mAb [59K71L12]

Purified Recombinant Rabbit Monoclonal Antibody

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货号 规格 价格
R010916
20µL ¥588.00
50µL ¥1080.00
100µL ¥1780.00

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Anti-SHP2 Rabbit mAb [59K71L12]
Anti-SHP2 Rabbit mAb [59K71L12]
Anti-SHP2 Rabbit mAb [59K71L12]
Anti-SHP2 Rabbit mAb [59K71L12]
Product NameAnti-SHP2 Rabbit mAb
DescriptionPurified Recombinant Rabbit Monoclonal Antibody
Application
  • Applications Legend:
  • WB=Western Blotting
  • IHC-P=Immunohistochemistry (Paraffin)
  • IHC-F=Immunohistochemistry (Frozen)
  • IP=Immunoprecipitation
  • IF=Immunofluorescence
  • IC=Immunochemistry
  • ICC=Immunocytochemistry
  • FC=Flow Cytometry
  • DB=Dot Blot
WB, IHC-P/IF (Tissue-P), IF (Cell)/ICC, ELISA
DilutionWB 1:1,000~1:2,000; IHC-P 1:100~1:200; IF 1:100~1:200
ReactivityHuman
HostRabbit
ClonalityMonoclonal
Clone No.59K71L12
IsotypeIgG
LabelUnconjugated
ImmunogenA synthesized peptide derived from human SHP2
FormatAffinity purified monoclonal antibody supplied in PBS with 0.02% sodium azide and 50% glycerol, pH 7.3.
SynonymsPTP2C; SHPTP2; PTPN11; Tyrosine-protein phosphatase non-receptor type 11; Protein-tyrosine phosphatase 1D; Protein-tyrosine phosphatase 2C; SH-PTP2; SH-PTP3; PTP-1D; PTP-2C; SHP-2; Shp2.
Molecular weightCalculated MW: 68 kDa; Observed MW: 68 kDa
Uniprot ID Q06124
Gene ID 5781
StorageShipped on wet ice. Store at -20℃. Stable for 24 months from date of receipt. Aliquoting is unnecessary for -20℃ storage.
PrecautionsAnti-SHP2 Rabbit mAb [59K71L12] is for research use only and not for use in diagnostic or therapeutic procedures.
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]
Cellular Location Cytoplasm.Nucleus.
Tissue Location Widely expressed, with highest levels in heart, brain, and skeletal muscle.

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