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Figure 1. Western blotting validation for Anti-mAChR M4 Antibody A08161-1 Western Blot (WB) analysis of specific cells using mAChR M4 polyclonal antibody. Electrophoresis was performed on a SDS-PAGE gel. To determine SDS-PAGE gel concentration
Figure 1. Western blotting validation for Anti-mAChR M4 Antibody A08161-1 Western Blot (WB) analysis of specific cells using mAChR M4 polyclonal antibody. Electrophoresis was performed on a SDS-PAGE gel. To determine SDS-PAGE gel concentration
Figure 1. Western blotting validation for Anti-mAChR M4 Antibody A08161-1 Western Blot (WB) analysis of specific cells using mAChR M4 polyclonal antibody. Electrophoresis was performed on a SDS-PAGE gel. To determine SDS-PAGE gel concentration

Anti-mAChR M4 Antibody

A08161-1
Boster Bio
ApplicationsImmunoFluorescence, Western Blot, ELISA
Product group Antibodies
ReactivityHuman, Mouse, Rat
TargetCHRM4
100 ul
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Overview

  • Supplier
    Boster Bio
  • Product Name
    Anti-mAChR M4 Antibody
  • Delivery Days Customer
    9
  • Applications
    ImmunoFluorescence, Western Blot, ELISA
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Concentration
    1 mg/ml
  • Gene ID1132
  • Target name
    CHRM4
  • Target description
    cholinergic receptor muscarinic 4
  • Target synonyms
    HM4, M4R, muscarinic acetylcholine receptor M4, acetylcholine receptor, muscarinic 4
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDP08173
  • Protein Name
    Muscarinic acetylcholine receptor M4
  • Scientific Description
    Boster Bio Anti-mAChR M4 Antibody catalog # A08161-1. Tested in WB, IF, ELISA applications. This antibody reacts with Human, Mouse, Rat.
  • Reactivity
    Human, Mouse, Rat
  • Storage Instruction
    -20°C,2°C to 8°C
  • UNSPSC
    12352203

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A431 (Positive) and Huvec (Negative control) cells (black) were incubated in 5% BSA blocking buffer for 30 min at room temperature. Cells were then stained with CHRM4/mAChR M4 Antibody (bs-11998R) at 1:50 dilution in blocking buffer and incubated for 30 min at room temperature, washed twice with 2% BSA in PBS, followed by secondary antibody(blue) incubation for 40 min at room temperature. Acquisitions of 20,000 events were performed. Cells stained with primary antibody (green), and isotype control (orange).
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