NNT-1 Polyclonal Antibody, 20ul Cell Proliferation Diseases associated with R3HCC1L include

Diseases associated with R3HCC1L include cutaneous anthrax

Mutations in this gene cause corneal fleck dystrophy (CFD)

This gene encodes the protein for complementation group L

The MutL-alpha heterodimer possesses an endonucleolytic activity that is activated following recognition of mismatches and insertion/deletion loops by the MutS-alpha and MutS-beta heterodimers

NNT-1 Polyclonal Antibody, 20ul Cell Proliferation Diseases associated with R3HCC1L includeThis gene is a member of the glycoprotein (gp)130 cytokine family and encodes cardiotrophin like cytokine factor 1 (CLCF1). CLCF1 forms a heterodimer complex with cytokine receptor like factor 1 (CRLF1). This dimer competes with ciliary neurotrophic factor (CNTF) for binding to the ciliary neurotrophic factor receptor (CNTFR) complex, and activates the Jak STAT signaling cascade. CLCF1 can be actively secreted from cells by forming a complex with