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Defects in the gene SHOXX cause Leri-Weill dyschondrosteosis (LWD) and Langer mesomelic dysplasia (LMD)
ESRRG Polyclonal Antibody Sizes: 50µl
Immunofluorescence analysis of A431 cells using TROP-2 Rabbit pAb at dilution of 1:100
Description: Detection and Quantification of Pyruvate Dehydrogenase Activity
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