B9D1 polyclonal, anti-human, mouse, rat

Background:
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.

Synonyms: B9, EPPB9, JBTS27, MKS9, MKSR1

Cellular Location: Cytoplasm cilium axoneme cilium basal body cytoskeleton

Immunogen:
Recombinant protein of human B9D1

Gene Symbol: B9D1

Gene ID: 27077

Swiss prot: Q9UPM9

Calculated MW: 23kDa

Recommended dilution:
WB 1:500-2000, IHC 1:50-200,

Purity:
Affinity purification

Storage Buffer:
Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3.

Storage:
Store at -20℃. Avoid freeze / thaw cycles.