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Western blot analysis of lysates from human skeletal muscle, mouse lung, rat lung tissue lysate (from left to right), using LMCD1 Antibody (C-term). A08888 was diluted at 1:1000 at each lane. A goat anti-rabbit IgG H&L (HRP) at 1:10000 dilution was used as the secondary antibody. Lysates at 20ug per lane.
Western blot analysis of lysates from human skeletal muscle, mouse lung, rat lung tissue lysate (from left to right), using LMCD1 Antibody (C-term). A08888 was diluted at 1:1000 at each lane. A goat anti-rabbit IgG H&L (HRP) at 1:10000 dilution was used as the secondary antibody. Lysates at 20ug per lane.
Western blot analysis of lysates from human skeletal muscle, mouse lung, rat lung tissue lysate (from left to right), using LMCD1 Antibody (C-term). A08888 was diluted at 1:1000 at each lane. A goat anti-rabbit IgG H&L (HRP) at 1:10000 dilution was used as the secondary antibody. Lysates at 20ug per lane.

Anti-LMCD1 Antibody (C-term)

A08888
Boster Bio
ApplicationsWestern Blot
Product group Antibodies
TargetLMCD1
80 ul
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Overview

  • Supplier
    Boster Bio
  • Product Name
    Anti-LMCD1 Antibody (C-term)
  • Delivery Days Customer
    9
  • Applications
    Western Blot
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Gene ID29995
  • Target name
    LMCD1
  • Target description
    LIM and cysteine rich domains 1
  • Target synonyms
    LIM and cysteine-rich domains protein 1, dyxin
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDQ9NZU5
  • Protein Name
    LIM and cysteine-rich domains protein 1
  • Scientific Description
    Boster Bio Anti-LMCD1 Antibody (C-term) (Catalog # A08888). Tested in WB application(s). This antibody reacts with Human, Mouse, Rat.
  • Storage Instruction
    -20°C,2°C to 8°C
  • UNSPSC
    12352203

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IHC image of CSB-PA873714LA01HU diluted at 1:300 and staining in paraffin-embedded human lung tissue performed on a Leica BondTM system. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4°C overnight. The primary is detected by a biotinylated secondary antibody and visualized using an HRP conjugated SP system.
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