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.
TCR Screening Services
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".
HMRF1L / MTRF1L plays a role in mitochondrial translation termination, and is thought to be a release factor that is involved in the dissociation of the complete protein from the final tRNA, the ribosome, and the cognate mRNA. This protein acts upon UAA and UAG stop codons, but has no in vitro activity against UGA, which encodes tryptophan in human mitochondrion, or, the mitochondrial non-cognate stop codons, AGA and AGG. This protein shares sequence similarity to bacterial release factors.
Immunohistochemical staining of paraffin-embedded liver tissue using anti-MTRF1L mouse monoclonal antibody. (Dilution 1:50).
Immunohistochemical staining of paraffin-embedded Adenocarcinoma of ovary tissue using anti-MTRF1L mouse monoclonal antibody. (Dilution 1:50).
Immunohistochemical staining of paraffin-embedded Carcinoma of liver tissue using anti-MTRF1L mouse monoclonal antibody. (Dilution 1:50).
Immunohistochemical staining of paraffin-embedded colon tissue using anti-MTRF1L mouse monoclonal antibody. (Dilution 1:50).
Anti-MTRF1L mouse monoclonal antibody immunofluorescent staining of COS7 cells transiently transfected by pCMV6-ENTRY MTRF1L.
Immunofluorescent staining of HT29 cells using anti-MTRF1L mouse monoclonal antibody.
HEK293T cells were transfected with the pCMV6-ENTRY control (Left lane) or pCMV6-ENTRY MTRF1L (Right lane) cDNA for 48 hrs and lysed. Equivalent amounts of cell lysates (5 ug per lane) were separated by SDS-PAGE and immunoblotted with anti-MTRF1L.
HEK293T cells transfected with either pCMV6-ENTRY MTRF1L (Red) or empty vector control plasmid (Blue) were immunostained with anti-MTRF1L mouse monoclonal, and then analyzed by flow cytometry.
Requested From: United States
Date Requested: 12/7/2016