MIP-1 Alpha Polyclonal Antibody, 100ul Cell Culture Dishes Defects in this gene cause

Defects in this gene cause congenital erythropoietic porphyria (Gunther's disease)

Two transcript variants encoding different isoforms have been described for RFX2

Effortlessly hold tubes in place with the VT1

Chloride conductance of these channels can be modulated by agents such as benzodiazepines that bind to the GABA-A receptor

For background information on the DNAJ family

MIP-1 Alpha Polyclonal Antibody, 100ul Cell Culture Dishes Defects in this gene causeCCL3 (C C motif chemokine ligand 3) represents a small inducible cytokine. The encoded protein, also known as macrophage inflammatory protein 1 alpha, plays a role in inflammatory responses through binding to the receptors CCR1, CCR4 and CCR5. Polymorphisms at this locus (CCL3) may be associated with both resistance and susceptibility to infection by human immunodeficiency virus type 1.