Pay in 4 interest-free payments of $46.25 Learn more
Ships within 48 hours · Estimated delivery Aug 10 - Aug 15
Live Spec
EBLN2 Rabbit Polyclonal Antibody, 50ul Enzymes Mutations in this gene are
Store: cgm.lt · Domain: cgm.lt
Mutations in this gene are associated with the autosomal recessive disorders cystic fibrosis and congenital bilateral aplasia of the vas deferens
Mutations in KRT17 lead to Jackson-Lawler type pachyonychia congenita and steatocystoma multiplex
The protein associates with several components of the extracellular signal-regulated kinase (ERK) pathway
The amino acid sequence of this enzyme is 86% identical to that of bovine glutaminyl cyclase
disease:Defects in CDKN2A are a cause of Li-Fraumeni syndrome (LFS)
EBLN2 Rabbit Polyclonal Antibody, 50ul Enzymes Mutations in this gene are
US$ 12.00
US$ 60.00
US$ 16.00
US$ 16.00
US$ 13.00
US$ 20.00
US$ 28.00
US$ 12.95
US$ 15.00
