B9D1 Polyclonal Antibody

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.

Research Area: Cell Biology

Synonyms:
B9D1, B9, EPPB9, JBTS27, MKS9, MKSR1

Immunogen: Recombinant fusion protein of human B9D1 (NP_056496.1).

Swissprot: Q9UPM9
Gene ID: 27077

Purification Method: Affinity purification

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

Concentration: 1 mg/mL
Dilution: IHC 1:50-1:200

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