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>   首页   >   产品   >   一抗   >   心血管   >   TCAP Antibody (monoclonal) (M01)   

TCAP Antibody (monoclonal) (M01)

Mouse monoclonal antibody raised against a full length recombinant TCAP.

     
  • 1 - TCAP Antibody (monoclonal) (M01) AT4174a
    Antibody Reactive Against Recombinant Protein.Western Blot detection against Immunogen (44.11 KDa) .
  • 10 - TCAP Antibody (monoclonal) (M01) AT4174a
    Detection limit for recombinant GST tagged TCAP is approximately 0.1ng/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, E
Primary Accession O15273
Other Accession BC012628
Reactivity Human
Host mouse
Clonality monoclonal
Isotype IgG1 kappa
Clone Names 2B1
Calculated MW 19052 Da
Additional Information
Gene ID 8557
Other Names Telethonin, Titin cap protein, TCAP
Target/Specificity TCAP (AAH12628, 1 a.a. ~ 167 a.a) full-length recombinant protein with GST tag. MW of the GST tag alone is 26 KDa.
Dilution WB~~1:500~1000
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.
PrecautionsTCAP 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

Sarcomere assembly is regulated by the muscle protein titin. Titin is a giant elastic protein with kinase activity that extends half the length of a sarcomere. It serves as a scaffold to which myofibrils and other muscle related proteins are attached. This gene encodes a protein found in striated and cardiac muscle that binds to the titin Z1-Z2 domains and is a substrate of titin kinase, interactions thought to be critical to sarcomere assembly. Mutations in this gene are associated with limb-girdle muscular dystrophy type 2G.

REFERENCES

Physiogenomic analysis of statin-treated patients: domain-specific counter effects within the ACACB gene on low-density lipoprotein cholesterol? Rua?o G, et al. Pharmacogenomics, 2010 Jul. PMID 20602615.A novel custom resequencing array for dilated cardiomyopathy. Zimmerman RS, et al. Genet Med, 2010 May. PMID 20474083.Common susceptibility variants examined for association with dilated cardiomyopathy. Rampersaud E, et al. Ann Hum Genet, 2010 Mar. PMID 20201937.The role of Lamin A/C mutations in Danish patients with idiopathic dilated cardiomyopathy. M?ller DV, et al. Eur J Heart Fail, 2009 Nov. PMID 19875404.Depletion of zebrafish Tcap leads to muscular dystrophy via disrupting sarcomere-membrane interaction, not sarcomere assembly. Zhang R, et al. Hum Mol Genet, 2009 Nov 1. PMID 19679566.

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