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".
IHC - Paraffin, Immunofluorescence, Western blot, Flow Cytometry
Rabbit Polyclonal to Human SPECC1 / CYTSB
Human SPECC1 / CYTSB
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.