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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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TRAT1 / TRIM Antibody (aa29‑186, clone TRIM‑4) LS‑C41080 Best Seller
TRIM antibody LS-C41080 is an unconjugated mouse monoclonal antibody to TRIM (TRAT1) from human and mouse. Validated for Flow, IF and WB.
Catalog
Size
Price
LS-C41080-100
100 µg
$325
Description
TRIM antibody LS-C41080 is an unconjugated mouse monoclonal antibody to TRIM (TRAT1) from human and mouse. Validated for Flow, IF and WB.
Target
Human TRAT1 / TRIM
Host
Mouse
Reactivity
Human, Mouse (tested or 100% immunogen sequence identity)
Clonality
IgG2a Monoclonal [TRIM-4]
Conjugations
Unconjugated
Purification
Affinity purified
Modifications
Unmodified
Applications
  • Immunofluorescence
  • Western blot
  • Flow Cytometry
Immunogen
TRAT1 / TRIM antibody was raised against recombinant human TRAT1 / TRIM.
Epitope
aa29-186
Specificity
Partial recombinant human TRIM (amino acids 29-186)
Presentation
Phosphate-buffered solution, pH 7.2, 0.09% sodium azide.
Restrictions
For research use only.
About TRAT1 / TRIM
Q6PIZ9 NM_016388 NP_057472.2

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Western blot

Extracts from peripheral blood mononuclear cells were resolved by electrophoresis, transferred to nitrocellulose, and probed with mouse monoclonal antibody against TRIM. Proteins were visualized using a goat anti-mouse secondary conjugated to HRP and a ch
Extracts from peripheral blood mononuclear cells were resolved by electrophoresis, transferred to nitrocellulose, and probed with mouse monoclonal antibody against TRIM. Proteins were visualized using a goat anti-mouse secondary conjugated to HRP and a ch

Western blot

Extracts from peripheral blood mononuclear cells were resolved by electrophoresis, transferred to nitrocellulose, and probed with mouse monoclonal antibody against TRIM. Proteins were visualized using a goat anti-mouse secondary conjugated to HRP and a ch
Extracts from peripheral blood mononuclear cells were resolved by electrophoresis, transferred to nitrocellulose, and probed with mouse monoclonal antibody against TRIM. Proteins were visualized using a goat anti-mouse secondary conjugated to HRP and a ch

Western blot

Extracts from peripheral blood mononuclear cells were resolved by electrophoresis, transferred to nitrocellulose, and probed with mouse monoclonal antibody against TRIM. Proteins were visualized using a goat anti-mouse secondary conjugated to HRP and a ch
Extracts from peripheral blood mononuclear cells were resolved by electrophoresis, transferred to nitrocellulose, and probed with mouse monoclonal antibody against TRIM. Proteins were visualized using a goat anti-mouse secondary conjugated to HRP and a ch

Western blot

Extracts from peripheral blood mononuclear cells were resolved by electrophoresis, transferred to nitrocellulose, and probed with mouse monoclonal antibody against TRIM. Proteins were visualized using a goat anti-mouse secondary conjugated to HRP and a ch
Extracts from peripheral blood mononuclear cells were resolved by electrophoresis, transferred to nitrocellulose, and probed with mouse monoclonal antibody against TRIM. Proteins were visualized using a goat anti-mouse secondary conjugated to HRP and a ch

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