B9D1 blocking peptide

GeneTex

B9D1 blocking peptide

9

Neutralisation/Blocking

Research Use Only

200 ug/ml

Unconjugated

This gene encodes a B9 domain-containing protein, one of several that are involved in ciliogenesis. Alterations in expression of this gene have been found in a family with Meckel syndrome. Meckel syndrome has been associated with at least six different genes. This gene is located within the Smith-Magenis syndrome region on chromosome 17. Three alternatively spliced transcript variants that encode different proteins have been described for this gene. [provided by RefSeq, Aug 2011]

-20°C

12352202