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SFT2D2 Antibody (N-term)

Peptide Affinity Purified Rabbit Polyclonal Antibody (Pab)

     
  • 1 - SFT2D2 Antibody (N-term) AP11150a
    SFT2D2 Antibody (N-term) (Cat. #AP11150a) western blot analysis in U251 cell line lysates (35ug/lane).This demonstrates the SFT2D2 antibody detected the SFT2D2 protein (arrow).
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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, E
Primary Accession O95562
Other Accession Q4FZV2, Q8VD57, NP_955376.1
Reactivity Human
Predicted Mouse, Rat
Host Rabbit
Clonality Polyclonal
Isotype Rabbit Ig
Calculated MW 17779 Da
Additional info
Gene ID 375035
Other Names Vesicle transport protein SFT2B, SFT2 domain-containing protein 2, SFT2D2 {ECO:0000312|EMBL:AAH680981}
Target/Specificity This SFT2D2 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 1-30 amino acids from the N-terminal region of human SFT2D2.
Dilution WB~~1:1000
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.
PrecautionsSFT2D2 Antibody (N-term) is for research use only and not for use in diagnostic or therapeutic procedures.
Protein Information
Name SFT2D2 {ECO:0000312|EMBL:AAH68098.1}
Function May be involved in fusion of retrograde transport vesicles derived from an endocytic compartment with the Golgi complex.
Cellular Location Membrane; Multi-pass membrane protein
Research Areas

BACKGROUND

PA2 catalyzes the calcium-dependent hydrolysis of the 2-acyl groups in 3-sn-phosphoglycerides. L-alpha-1-palmitoyl-2-linoleoyl phosphatidylethanolamine is more efficiently hydrolyzed than the other phospholipids examined.

REFERENCES

Ehret, G.B., et al. Eur. J. Hum. Genet. 17(12):1650-1657(2009)
Cheung, C.L., et al. Hum. Mol. Genet. 18(4):679-687(2009)
Lamesch, P., et al. Genomics 89(3):307-315(2007)
Clark, H.F., et al. Genome Res. 13(10):2265-2270(2003)

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