Tubulin alpha 1/3/4(Phospho Tyr272) Polyclonal Antibody, 100ul Long RNA Synthesis Bardet-Biedl syndrome is an autosomal

Bardet-Biedl syndrome is an autosomal recessive disorder characterized by severe pigmentary retinopathy

KRT16 and KRT18

Catalytic activity:Hydrolysis of an N(6)-acetyl-lysine residue of a histone to yield a deacetylated histone

This gene encodes the integrin alpha M chain

The encoded protein may be required for normal galactose metabolism by maintaining the equilibrium of alpha and beta anomers of galactose

Tubulin alpha 1/3/4(Phospho Tyr272) Polyclonal Antibody, 100ul Long RNA Synthesis Bardet-Biedl syndrome is an autosomalMicrotubules of the eukaryotic cytoskeleton perform essential and diverse functions and are composed of a heterodimer of alpha and beta tubulins. The genes encoding these microtubule constituents belong to the tubulin superfamily, which is composed of six distinct families. Genes from the alpha, beta and gamma tubulin families are found in all eukaryotes. The alpha and beta tubulins represent the major components of microtubules, while gamma tubulin