Pay in 4 interest-free payments of $42.82 Learn more
Ships within 48 hours · Estimated delivery Jul 28 - Aug 2
Defects in the gene SHOXX cause Leri-Weill dyschondrosteosis (LWD) and Langer mesomelic dysplasia (LMD)
BS6993-100
Description: Detection and Quantification of Pyruvate Dehydrogenase Activity
which binds to DNA double-strand break ends and is required for the non-homologous end joining (NHEJ) pathway of DNA repair
Immunogen: A synthesized peptide derived from human IGFL4
TRMT2A/HTF9C Polyclonal Antibody-BS70767 Size:100µl Defects in the gene SHOXXTRMT2A HTF9C Polyclonal Antibody Sizes: 50l, 100l Catalogue Numbers: BS70767 50, BS70767 100 Product: 1mg ml in PBS with 0. 02% sodium azide, 50% glycerol, pH7. 2 Swiss Prot: Q8IZ69 Host: Rabbit Reactivity: Human, Mouse, Rat Applications: WB, IHC All Applications: WB,1: 500 1: 1000 IHC,1: 50 1: 200 Background: The protein encoded by this gene is of unknown function. However, it is orthologous to the mouse Trmt2a gene and contains an RNA