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>   首页   >   产品   >   一抗   >   细胞生物学   >   SPDYE1 Antibody (C-term)   

SPDYE1 Antibody (C-term)

Peptide Affinity Purified Rabbit Polyclonal Antibody (Pab)

     
  • 1 - SPDYE1 Antibody (C-term) AP11296b
    SPDYE1 Antibody (C-term) (Cat. #AP11296b) western blot analysis in HepG2 cell line lysates (35ug/lane).This demonstrates the SPDYE1 antibody detected the SPDYE1 protein (arrow).
  • 4 - SPDYE1 Antibody (C-term) AP11296b
    SPDYE1 Antibody (C-term) (Cat. #AP11296b) flow cytometric analysis of HepG2 cells (right histogram) compared to a negative control cell (left histogram).FITC-conjugated goat-anti-rabbit secondary antibodies were used for the analysis.
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Product info
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, FC, E
Primary Accession Q8NFV5
Other Accession NP_778234.2
Reactivity Human
Host Rabbit
Clonality Polyclonal
Isotype Rabbit Ig
Calculated MW 40668 Da
Additional info
Gene ID 285955
Other Names Speedy protein E1, Williams-Beuren syndrome chromosomal region 19 protein, SPDYE1, WBSCR19
Target/Specificity This SPDYE1 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 242-271 amino acids from the C-terminal region of human SPDYE1.
Dilution WB~~1:1000
FC~~1:10~50
Format Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is purified through a protein A column, followed by peptide affinity purification.
StorageMaintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles.
PrecautionsSPDYE1 Antibody (C-term) is for research use only and not for use in diagnostic or therapeutic procedures.
Protein Information
Name SPDYE1
Synonyms WBSCR19
Research Areas

BACKGROUND

This gene is located at chromosome 7p13 which is close to the Williams Beuren syndrome chromosome region 7q11.23. [provided by RefSeq].

REFERENCES

Dinarina, A., et al. Biochem. J. 386 (PT 2), 349-355 (2005) :
Merla, G., et al. Hum. Genet. 110(5):429-438(2002)

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