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>   首页   >   产品   >   一抗   >   信号转导   >   EMD Antibody (monoclonal) (M01)   

EMD Antibody (monoclonal) (M01)

Mouse monoclonal antibody raised against a partial recombinant EMD.

     
  • 1 - EMD Antibody (monoclonal) (M01) AT1898a
    Antibody Reactive Against Recombinant Protein.Western Blot detection against Immunogen (37.84 KDa) .
  • 1 - EMD Antibody (monoclonal) (M01) AT1898a
    EMD monoclonal antibody (M01), clone 3B9 Western Blot analysis of EMD expression in HeLa ( (Cat # AT1898a )
  • 2 - EMD Antibody (monoclonal) (M01) AT1898a
    Immunoperoxidase of monoclonal antibody to EMD on formalin-fixed paraffin-embedded human tonsil. [antibody concentration 1 ug/ml]
  • 3 - EMD Antibody (monoclonal) (M01) AT1898a
    Immunofluorescence of monoclonal antibody to EMD on HeLa cell. [antibody concentration 10 ug/ml]
  • 10 - EMD Antibody (monoclonal) (M01) AT1898a
    Detection limit for recombinant GST tagged EMD is approximately 0.03ng/ml as a capture antibody.
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Product Information
Application
  • Applications Legend:
  • E=ELISA
  • WB=Western Blotting
  • IHC=Immunohistochemistry
  • IHC-P=Immunohistochemistry (Paraffin)
  • IP=Immunoprecipitation
  • IF=Immunofluorescence
  • IC=Immunochemistry
  • ICC=Immunocytochemistry
  • FC=Flow Cytometry
  • DB=Dot Blot
WB, IHC, IF, E
Primary Accession P50402
Other Accession BC000738
Reactivity Human
Host mouse
Clonality monoclonal
Isotype IgG2a Kappa
Clone Names 3B9
Calculated MW 28994 Da
Additional Information
Gene ID 2010
Other Names Emerin, EMD, EDMD, STA
Target/Specificity EMD (AAH00738, 1 a.a. ~ 110 a.a) partial recombinant protein with GST tag. MW of the GST tag alone is 26 KDa.
Dilution WB~~1:500~1000
IHC~~1:100~500
IF~~1:50~200
E~~N/A
Format Clear, colorless solution in phosphate buffered saline, pH 7.2 .
StorageStore at -20°C or lower. Aliquot to avoid repeated freezing and thawing.
PrecautionsEMD Antibody (monoclonal) (M01) is for research use only and not for use in diagnostic or therapeutic procedures.
Research Areas

For Research Use Only. Not For Use In Diagnostic Procedures.

BACKGROUND

Emerin is a serine-rich nuclear membrane protein and a member of the nuclear lamina-associated protein family. It mediates membrane anchorage to the cytoskeleton. Dreifuss-Emery muscular dystrophy is an X-linked inherited degenerative myopathy resulting from mutation in the emerin gene.

REFERENCES

Variation at the NFATC2 Locus Increases the Risk of Thiazolinedinedione-Induced Edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) Study. Bailey SD, et al. Diabetes Care, 2010 Jul 13. PMID 20628086.A novel custom resequencing array for dilated cardiomyopathy. Zimmerman RS, et al. Genet Med, 2010 May. PMID 20474083.Emery-Dreifuss dystrophy: a 4-year follow-up on a laminopathy of special interest. Hausmanowa-Petrusewicz I, et al. Neurol Neurochir Pol, 2009 Sep-Oct. PMID 20054742.Gene-centric association signals for lipids and apolipoproteins identified via the HumanCVD BeadChip. Talmud PJ, et al. Am J Hum Genet, 2009 Nov. PMID 19913121.Tyrosine phosphorylation of nuclear-membrane protein emerin by Src, Abl and other kinases. Tifft KE, et al. J Cell Sci, 2009 Oct 15. PMID 19789182.

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