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LHFPL1 Antibody (N-term)

Affinity Purified Rabbit Polyclonal Antibody (Pab)

     
  • WB - LHFPL1 Antibody (N-term) AP13197a
    LHFPL1 Antibody (N-term) (Cat. #AP13197a) western blot analysis in human placenta tissue lysates (35ug/lane).This demonstrates the LHFPL1 antibody detected the LHFPL1 protein (arrow).
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Product Information
Application
  • Applications Legend:
  • WB=Western Blot
  • IHC=Immunohistochemistry
  • IHC-P=Immunohistochemistry (Paraffin-embedded Sections)
  • IHC-F=Immunohistochemistry (Frozen Sections)
  • IF=Immunofluorescence
  • FC=Flow Cytopmetry
  • IC=Immunochemistry
  • ICC=Immunocytochemistry
  • E=ELISA
  • IP=Immunoprecipitation
  • DB=Dot Blot
  • CHIP=Chromatin Immunoprecipitation
  • FA=Fluorescence Assay
  • IEM=Immunoelectronmicroscopy
  • EIA=Enzyme Immunoassay
WB, E
Primary Accession Q86WI0
Other Accession NP_835469.1
Reactivity Human
Host Rabbit
Clonality Polyclonal
Isotype Rabbit IgG
Calculated MW 23777 Da
Antigen Region 20-49 aa
Additional Information
Gene ID 340596
Other Names Lipoma HMGIC fusion partner-like 1 protein, LHFPL1
Target/Specificity This LHFPL1 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 20-49 amino acids from the N-terminal region of human LHFPL1.
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.
PrecautionsLHFPL1 Antibody (N-term) is for research use only and not for use in diagnostic or therapeutic procedures.
Protein Information
Name LHFPL1 (HGNC:6587)
Cellular Location Membrane; Multi-pass membrane protein
Tissue Location Widely expressed. Expressed at high levels in lung, thymus, skeletal muscle, colon and ovary
Research Areas
Citations (0)
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Background

This gene is a member of the lipoma HMGIC fusion partner (LHFP) gene family, which is a subset of the superfamily of tetraspan transmembrane protein encoding genes. Mutations in one LHFP-like gene result in deafness in humans and mice, and a second LHFP-like gene is fused to a high-mobility group gene in a translocation-associated lipoma. Alternatively spliced transcript variants have been found, but their biological validity has not been determined.

References

Longo-Guess, C.M., et al. Proc. Natl. Acad. Sci. U.S.A. 102(22):7894-7899(2005)
Huang, C., et al. DNA Seq. 15(4):299-302(2004)
Petit, M.M., et al. Genomics 57(3):438-441(1999)

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$ 365.00
$ 140.00
Cat# AP13197a
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