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Anti-B9D1 Antibody Polyclonal
Also for B9D1 (NM_015681)
|B9D1 antibody was raised against an 18 amino acid synthetic peptide near the carboxy terminus of human B9D1.|
||WB: 1 ug/ml, ICC: 5 ug/ml, IF: 20 ug/ml
|B9D1 Antibody is supplied in PBS containing 0.02% sodium azide.|
|B9D1 Antibody is affinity chromatography purified via peptide column.
|Homo sapiens B9 protein domain 1 (B9D1), transcript variant 2|
|B9; EPPB9; MKS9; MKSR1|
|B9D1 Antibody: Meckel syndrome (MKS) is an embryonic lethal, autosomal recessive disorder characterized by polycystic kidney disease, central nervous system defects, polydactyly and liver fibrosis. B9D1 is 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. B9D1, and its related protein B9D2, form a complex with MKS1, disruption of which causes MKS. B9D1 is thought to be required for normal hedgehog signaling, ciliogenesis, and ciliary protein localization.|
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Western blot analysis of B9D1 in 293 cell lysate with B9D1 antibody at 1 ug/mL in (A) the absence and (B) the presence of blocking peptide.
Immunocytochemistry of B9D1 in 293 cells with B9D1 antibody at 5 ug/mL.
Immunofluorescence of B9D1 in 293 cells with B9D1 antibody at 20 ug/mL.