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Work with LifeSpan to design a custom immunohistochemistry to address your specific biological question. Outsource the entire localization process without having to worry about finding and characterizing target specific antibodies, sourcing and validating difficult-to-find tissues, and having the ability to interpret the resulting immunostaining in relation to complex human pathologies.

Test your therapeutic antibodies in immunohistochemistry against a broad panel of normal frozen human tissue types in order to determine potential unintended binding. Our non-GLP TCR services are designed on the FDA recommendation outlined in their "Points to Consider in the Manufacture and Testing of Monoclonal Antibody Products for Human Use".

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GSR / Glutathione Reductase Antibody (clone AT11D10) LS‑C755474
Glutathione Reductase antibody LS-C755474 is an unconjugated mouse monoclonal antibody to human Glutathione Reductase (GSR). Validated for ELISA, Flow, ICC and WB.
Catalog
Size
Price
LS-C755474-50
50 µl (1 mg/ml)
$255
LS-C755474-100
100 µl (1 mg/ml)
$315

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Product Description

Glutathione Reductase antibody LS-C755474 is an unconjugated mouse monoclonal antibody to human Glutathione Reductase (GSR). Validated for ELISA, Flow, ICC and WB.

Specifications

Target
Human GSR / Glutathione Reductase
Synonyms
GSR, GR, GLUR, GRase, Glutathione reductase, GRD1
Host
Mouse
Reactivity
Human (tested or 100% immunogen sequence identity)
Clonality
IgG1,k Monoclonal [AT11D10]
Conjugations
Unconjugated
Purification
Protein A affinity chromatography
Modifications
Unmodified
Applications
  • ICC (1:100)
  • Western blot (1:500)
  • Flow Cytometry
  • ELISA
Immunogen
Recombinant human GSR (43-522aa) purified from E.coli
Usage
Applications should be user optimized.
Presentation
PBS, pH 7.4, 0.02% Sodium Azide, 10% Glycerol
Restrictions
For research use only.
About GSR / Glutathione Reductase
GSR / Glutathione Reductase is a member of the class-I pyridine nucleotide-disulfide oxidoreductase family. This enzyme is a homodimeric flavoprotein. It is a central enzyme of cellular antioxidant defense, and reduces oxidized glutathione disulfide (GSSG) to the sulfhydryl form GSH, which is an important cellular antioxidant. Rare mutations in this gene result in hereditary glutathione reductase deficiency. P00390 NM_000637 NP_000628.2


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Images

Immunofluorescence

ICC/IF analysis of GSR in HeLa cells line, stained with DAPI (Blue) for nucleus staining and monoclonal anti-human GSR antibody (1:100) with goat anti-mouse IgG-Alexa fluor 488 conjugate (Green).
ICC/IF analysis of GSR in HeLa cells line, stained with DAPI (Blue) for nucleus staining and monoclonal anti-human GSR antibody (1:100) with goat anti-mouse IgG-Alexa fluor 488 conjugate (Green).

Western blot

The cell lysates of HeLa, Jurkat and 293T(40ug) were resolved by SDS-PAGE, transferred to PVDF membrane and probed with anti-human GSR antibody (1:500). Proteins were visualized using a goat anti-mouse secondary antibody conjugated to HRP and an ECL detection system.
The cell lysates of HeLa, Jurkat and 293T(40ug) were resolved by SDS-PAGE, transferred to PVDF membrane and probed with anti-human GSR antibody (1:500). Proteins were visualized using a goat anti-mouse secondary antibody conjugated to HRP and an ECL detection system.

Immunofluorescence

ICC/IF analysis of GSR in HeLa cells line, stained with DAPI (Blue) for nucleus staining and monoclonal anti-human GSR antibody (1:100) with goat anti-mouse IgG-Alexa fluor 488 conjugate (Green).
ICC/IF analysis of GSR in HeLa cells line, stained with DAPI (Blue) for nucleus staining and monoclonal anti-human GSR antibody (1:100) with goat anti-mouse IgG-Alexa fluor 488 conjugate (Green).

Western blot

The cell lysates of HeLa, Jurkat and 293T(40ug) were resolved by SDS-PAGE, transferred to PVDF membrane and probed with anti-human GSR antibody (1:500). Proteins were visualized using a goat anti-mouse secondary antibody conjugated to HRP and an ECL detection system.
The cell lysates of HeLa, Jurkat and 293T(40ug) were resolved by SDS-PAGE, transferred to PVDF membrane and probed with anti-human GSR antibody (1:500). Proteins were visualized using a goat anti-mouse secondary antibody conjugated to HRP and an ECL detection system.

Immunofluorescence

ICC/IF analysis of GSR in HeLa cells line, stained with DAPI (Blue) for nucleus staining and monoclonal anti-human GSR antibody (1:100) with goat anti-mouse IgG-Alexa fluor 488 conjugate (Green).
ICC/IF analysis of GSR in HeLa cells line, stained with DAPI (Blue) for nucleus staining and monoclonal anti-human GSR antibody (1:100) with goat anti-mouse IgG-Alexa fluor 488 conjugate (Green).

Western blot

The cell lysates of HeLa, Jurkat and 293T(40ug) were resolved by SDS-PAGE, transferred to PVDF membrane and probed with anti-human GSR antibody (1:500). Proteins were visualized using a goat anti-mouse secondary antibody conjugated to HRP and an ECL detection system.
The cell lysates of HeLa, Jurkat and 293T(40ug) were resolved by SDS-PAGE, transferred to PVDF membrane and probed with anti-human GSR antibody (1:500). Proteins were visualized using a goat anti-mouse secondary antibody conjugated to HRP and an ECL detection system.

Immunofluorescence

ICC/IF analysis of GSR in HeLa cells line, stained with DAPI (Blue) for nucleus staining and monoclonal anti-human GSR antibody (1:100) with goat anti-mouse IgG-Alexa fluor 488 conjugate (Green).
ICC/IF analysis of GSR in HeLa cells line, stained with DAPI (Blue) for nucleus staining and monoclonal anti-human GSR antibody (1:100) with goat anti-mouse IgG-Alexa fluor 488 conjugate (Green).

Western blot

The cell lysates of HeLa, Jurkat and 293T(40ug) were resolved by SDS-PAGE, transferred to PVDF membrane and probed with anti-human GSR antibody (1:500). Proteins were visualized using a goat anti-mouse secondary antibody conjugated to HRP and an ECL detection system.
The cell lysates of HeLa, Jurkat and 293T(40ug) were resolved by SDS-PAGE, transferred to PVDF membrane and probed with anti-human GSR antibody (1:500). Proteins were visualized using a goat anti-mouse secondary antibody conjugated to HRP and an ECL detection system.

Requested From: United States
Date Requested: 11/12/2018

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