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Figure 1. Western blot analysis of SHQ1 using anti-SHQ1 antibody (A10185-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample unde r reducing conditions. Lane 1: human A549 whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human MOLT-4 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SHQ1 antigen affinity purified polyclonal antibody (Catalog # A10185-1) at 0.5 microg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SHQ1 at approximately 80 kDa. The expected band size for SHQ1 is at 65 kDa.
Figure 1. Western blot analysis of SHQ1 using anti-SHQ1 antibody (A10185-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample unde r reducing conditions. Lane 1: human A549 whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human MOLT-4 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SHQ1 antigen affinity purified polyclonal antibody (Catalog # A10185-1) at 0.5 microg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SHQ1 at approximately 80 kDa. The expected band size for SHQ1 is at 65 kDa.
Figure 1. Western blot analysis of SHQ1 using anti-SHQ1 antibody (A10185-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample unde r reducing conditions. Lane 1: human A549 whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human MOLT-4 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SHQ1 antigen affinity purified polyclonal antibody (Catalog # A10185-1) at 0.5 microg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SHQ1 at approximately 80 kDa. The expected band size for SHQ1 is at 65 kDa.

Anti-SHQ1 Antibody Picoband(r)

A10185-1-IFLUOR647
Boster Bio
TargetSHQ1
Product group Antibodies
100 ug
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Overview

  • Supplier
    Boster Bio
  • Product Name
    Anti-SHQ1 Antibody Picoband(r)
  • Delivery Days Customer
    9
  • Concentration
    500 ug/ml
  • Gene ID55164
  • Target name
    SHQ1
  • Target description
    SHQ1, H/ACA ribonucleoprotein assembly factor
  • Target synonyms
    gene associated with retinoid and interferon-induced mortality 1; GRIM-1; protein SHQ1 homolog; SHQ1 homolog; Shq1p
  • Protein IDQ6PI26
  • Protein Name
    Protein SHQ1 homolog
  • Scientific Description
    Boster Bio Anti-SHQ1 Antibody Picoband® catalog # A10185-1. Tested in ELISA, Flow Cytometry, IF, IHC, ICC, WB applications. This antibody reacts with Human, Mouse, Rat. 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

References

  • SHQ1 is required prior to NAF1 for assembly of H/ACA small nucleolar and telomerase RNPs. Grozdanov PN et al., 2009 Jun, RNA
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