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The antibody against B9D1 was raised in rabbit using the Recombinant Human B9 domain-containing protein 1 protein (1-130AA) as the immunogen. This antibody exists as a non-conjugated isotype IgG, Antigen affinity purified. This antibody has been validated on ELISA, IHC.
The antibody against B9D1 was raised in rabbit using the Recombinant Human B9 domain-containing protein 1 protein (1-130AA) as the immunogen. This antibody exists as a non-conjugated isotype IgG, Antigen affinity purified. This antibody has been validated on ELISA, IHC.
$299.00
| Cat.No | ADC-16753A | Clonality | Polyclonal |
|---|---|---|---|
| Host Species | Rabbit | Target Name | B9D1 |
| Target Synonyms | B9D1 antibody; MKSR1B9 domain-containing protein 1 antibody; MKS1-related protein 1 antibody | Form | Liquid |
| Species Reactivity | Human | Isotype | IgG |
| Storage Buffer | 50% Glycerol, PBS with 0.02% sodium azide, pH7.3. | Purification Method | Antigen affinity purified |
| Conjugate | Non-conjugated | Application | ELISA, IHC |
| Storage | Upon receipt |
| Immunogen Description | Recombinant Human B9 domain-containing protein 1 protein (1-130AA) | Target Species | Human |
|---|---|---|---|
| Immunogen Sequence | Complete sequences for the immunogen, target protein, and peptides are available upon request. | Uniprot ID | Q9UPM9 |
Uniprot Id
Q9UPM9
Target Species
Human
Target Name
B9D1
Target Full Name
B9 domain-containing protein 1
Target Function
Component of the tectonic-like complex, a complex localized at the transition zone of primary cilia and acting as a barrier that prevents diffusion of transmembrane proteins between the cilia and plasma membranes. Required for ciliogenesis and sonic hedgehog/SHH signaling.
Target Involvement
Meckel syndrome 9 (MKS9); Joubert syndrome 27 (JBTS27)
Target Subcellular Location
Cytoplasm, cytoskeleton, cilium basal body. Cytoplasm, cytoskeleton, cilium axoneme.
Target Protein Families
B9D family
Target Synonyms
B9D1; MKSR1B9 domain-containing protein 1; MKS1-related protein 1
Target 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.
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