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GTF2I Antibody (monoclonal) (M01)

Mouse monoclonal antibody raised against a full length recombinant GTF2I.

     
  • 1 - GTF2I Antibody (monoclonal) (M01) AT2289a
    Antibody Reactive Against Recombinant Protein.Western Blot detection against Immunogen (52.03 KDa) .
  • 1 - GTF2I Antibody (monoclonal) (M01) AT2289a
    GTF2I monoclonal antibody (M01), clone 3E2. Western Blot analysis of GTF2I expression in human colon.
  • 2 - GTF2I Antibody (monoclonal) (M01) AT2289a
    Immunoperoxidase of monoclonal antibody to GTF2I on formalin-fixed paraffin-embedded human placenta. [antibody concentration 3 ug/ml]
  • 3 - GTF2I Antibody (monoclonal) (M01) AT2289a
    Immunofluorescence of monoclonal antibody to GTF2I on HeLa cell . [antibody concentration 10 ug/ml]
  • 10 - GTF2I Antibody (monoclonal) (M01) AT2289a
    Detection limit for recombinant GST tagged GTF2I 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 P78347
Other Accession BC004472
Reactivity Human
Host mouse
Clonality monoclonal
Isotype IgG2a Kappa
Clone Names 3E3
Calculated MW 112416 Da
Additional Information
Gene ID 2969
Other Names General transcription factor II-I, GTFII-I, TFII-I, Bruton tyrosine kinase-associated protein 135, BAP-135, BTK-associated protein 135, SRF-Phox1-interacting protein, SPIN, Williams-Beuren syndrome chromosomal region 6 protein, GTF2I, BAP135, WBSCR6
Target/Specificity GTF2I (AAH04472.1, 36 a.a. ~ 274 a.a) full-length 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.
PrecautionsGTF2I 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

This gene encodes a multifunctional phosphoprotein with roles in transcription and signal transduction. It is deleted in Williams-Beuren syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at chromosome 7q11.23. Alternative splicing results in multiple transcript variants. Related pseudogenes have been identified on chromosomes 7, 13 and 21.

REFERENCES

1.An SNP in an ultraconserved regulatory element affects Dlx5/Dlx6 regulation in the forebrain.Poitras L, Yu M, Lesage-Pelletier C, Macdonald RB, Gagne JP, Hatch G, Kelly I, Hamilton SP, Rubenstein JL, Poirier GG, Ekker M.Development. 2010 Sep;137(18):3089-97. Epub 2010 Aug 11.

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