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| Cat.No | ACP12742 | Target Name | POC1B |
|---|---|---|---|
| Form | Lyophilized powder | Expression System | Custom Production. Please inquire and provide the desire expression system. |
| Expression Range | 1-478 | Protein Length | Full length protein |
| Purity | >85% (SDS-PAGE) | Storage Buffer | 5%-50% glycerol. Lyophilized powder form: the buffer before lyophilization is Tris/PBS-based buffer, 6% Trehalose, Liquid form: default storage buffer is Tris/PBS-based buffer, pH 8.0. |
| Target Species | Human | Uniprot ID | Q8TC44 |
|---|
Uniprot Id
Q8TC44
Target Species
Human
Target Name
POC1B
Target Full Name
POC1 centriolar protein homolog B
Target Function
Plays an important role in centriole assembly and/or stability and ciliogenesis. Involved in early steps of centriole duplication, as well as in the later steps of centriole length control. Acts in concert with POC1A to ensure centriole integrity and proper mitotic spindle formation. Required for primary cilia formation, ciliary length and also cell proliferation. Required for retinal integrity.
Target Involvement
Cone-rod dystrophy 20 (CORD20)
Target Subcellular Location
Cytoplasm, cytoskeleton, microtubule organizing center, centrosome. Cytoplasm, cytoskeleton, microtubule organizing center, centrosome, centriole. Cytoplasm, cytoskeleton, cilium basal body. Cytoplasm, cytoskeleton, spindle pole.
Target Protein Families
WD repeat POC1 family
Target Tissue Specificity
Expressed in the retina.
Target Synonyms
4933430F16Rik; FLJ14923; FLJ41111; Pix1; POC1 centriolar protein homolog B (Chlamydomonas); POC1 centriolar protein homolog B; POC1B; POC1B_HUMAN; TUWD12; WD repeat containing protein 51B; WD repeat domain 51B; WD repeat-containing protein 51B; WDR51B
Target Background
POC1 proteins contain an N-terminal WD40 domain and a C-terminal coiled coil domain and are part of centrosomes. They play an important role in basal body and cilia formation. This gene encodes one of the two POC1 proteins found in humans. Mutation in this gene result in autosomal-recessive cone-rod dystrophy. Alternative splicing results in multiple transcript variants.
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