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Figure 2. Flow Cytometry analysis of U20S cells using anti-NAT8L antibody (A07393-2). Overlay histogram showing U20S cells stained with A07393-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NAT8L Antibody (A07393-2, 1microg/1x106 cells) for 30 min at 20°C. DyLight?488 conjugated goat anti-rabbit IgG (BA1127, 5-10microg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1microg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
Figure 2. Flow Cytometry analysis of U20S cells using anti-NAT8L antibody (A07393-2). Overlay histogram showing U20S cells stained with A07393-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NAT8L Antibody (A07393-2, 1microg/1x106 cells) for 30 min at 20°C. DyLight?488 conjugated goat anti-rabbit IgG (BA1127, 5-10microg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1microg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
Figure 2. Flow Cytometry analysis of U20S cells using anti-NAT8L antibody (A07393-2). Overlay histogram showing U20S cells stained with A07393-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NAT8L Antibody (A07393-2, 1microg/1x106 cells) for 30 min at 20°C. DyLight?488 conjugated goat anti-rabbit IgG (BA1127, 5-10microg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1microg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.

Anti-NAT8L Antibody Picoband(r)

A07393-2-CARRIER-FREE
Boster Bio
ApplicationsFlow Cytometry, Western Blot
Product group Antibodies
TargetNAT8L
100 ug
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Overview

  • Supplier
    Boster Bio
  • Product Name
    Anti-NAT8L Antibody Picoband(r)
  • Delivery Days Customer
    9
  • Applications
    Flow Cytometry, Western Blot
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Concentration
    500 ug/ml
  • Gene ID339983
  • Target name
    NAT8L
  • Target description
    N-acetyltransferase 8 like
  • Target synonyms
    CML3, NACED, NAT8-LIKE, N-acetylaspartate synthetase, N-acetyltransferase 8-like (GCN5-related, putative), NAA synthetase, Shati, camello-like protein 3
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDQ8N9F0
  • Protein Name
    N-acetylaspartate synthetase
  • Scientific Description
    Boster Bio Anti-NAT8L Antibody Picoband® catalog # A07393-2. Tested in Flow Cytometry, WB applications. This antibody reacts with Human. The brand Picoband indicates this is a premium antibody that guarantees superior quality, high affinity, and strong signals with minimal background in Western blot applications. Only our best-performing antibodies are designated as Picoband, ensuring unmatched performance.
  • Storage Instruction
    -20°C,2°C to 8°C
  • UNSPSC
    12352203