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".
Human (tested or 100% immunogen sequence identity)
Specificity and Use
SPECC1 / CYTSB antibody was raised against an internal synthetic peptide made to the human NSP5a3a protein sequence (between residues 200-300).
This antibody is specific for NSP5a3a. Species cross-reactivity: This antibody reacts with human protein. Other species have not been tested. There is 100% identity/homology of the immunogen with the human NSP5a3a protein. There is 93% homology of the immunogen with the mouse protein and 87% homology of the immunogen with the rat NSP5a3a protein.
SPECC1 Antibody, CYTSB Antibody, Cytospin-B Antibody, HCMOGT-1 Antibody, Structure protein NSP5a3b Antibody, Structure protein NSP5b3a Antibody, Structure protein NSP5b3b Antibody, Structure protein NSP5a3a Antibody, HCMOGT1 Antibody, NSP Antibody, NSP5 Antibody, Nuclear structure protein 5 Antibody, Sperm antigen HCMOGT-1 Antibody
The protein encoded by this gene belongs to the cytospin-A family. It is localized in the nucleus, and highly expressed in testis and some cancer cell lines. A chromosomal translocation involving this gene and platelet-derived growth factor receptor, beta gene (PDGFRB) may be a cause of juvenile myelomonocytic leukemia. Alternatively spliced transcript variants encoding different isoforms have been described for this gene.