Beta Tubulin Polyclonal Antibody, 50ul Cell Culture Dishes Defects in this gene can

Defects in this gene can also cause cone-rod dystrophy type 11| a disease characterized by the initial degeneration of cone photoreceptor cells and resulting in loss of color vision and visual acuity| followed by the degeneration of rod photoreceptor cells| which progresses to night blindness and the loss of peripheral vision

PubMed: 19131338

The intercellular adhesion molecule 2 encoded by ICAM2 is a member of the intercellular adhesion molecule (ICAM) family

This gene is located in the class III region of the human major histocompatibility complex

The parkin co-regulated gene protein forms a large molecular complex with chaperones| including heat shock proteins 70 and 90| and chaperonin components

Beta Tubulin Polyclonal Antibody, 50ul Cell Culture Dishes Defects in this gene canTUBB3 encodes a class III member of the beta tubulin protein family. Beta tubulins are one of two core protein families (alpha and beta tubulins) that heterodimerize and assemble to form microtubules. This protein is primarily expressed in neurons and may be involved in neurogenesis and axon guidance and maintenance. Mutations in TUBB3 are the cause of congenital fibrosis of the extraocular muscles type 3. Alternate splicing results in multiple