KCTD17 polyclonal, anti-human
€295.00
In stock
SKU
K106994P
Catalog Number: K106994P
Size: 100 μl
Other size: 50 μl
Isotype: RabbitIgG
Applications: IHC
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Questions? Contact us!
Size: 100 μl
Other size: 50 μl
Isotype: RabbitIgG
Applications: IHC
Request Manual
Questions? Contact us!
Background:
This gene encodes a protein that belongs to a conserved family of potassium channel tetramerization domain (KCTD)-containing proteins. The encoded protein functions in ciliogenesis by acting as a substrate adaptor for the cullin3-based ubiquitin-conjugating enzyme E3 ligase, and targets trichoplein, a keratin-binding protein, for degradation via polyubiquitinylation. A mutation in this gene is associated with autosomal dominant myoclonic dystonia 26.
Synonyms: FLJ12242
Cellular Location: Cytoplasm
Immunogen:
Recombinant protein of human KCTD17
Gene Symbol: KCTD17
Gene ID: 79734
Swiss prot: Q8N5Z5
Calculated MW: 36kDa
Recommended dilution:
IHC 1:50-200
Purity:
Affinity purification
Storage Buffer:
Buffer: PBS with 0.03% Proclin300, 50% glycerol, pH7.3.
Storage:
Store at -20℃. Avoid freeze / thaw cycles.
This gene encodes a protein that belongs to a conserved family of potassium channel tetramerization domain (KCTD)-containing proteins. The encoded protein functions in ciliogenesis by acting as a substrate adaptor for the cullin3-based ubiquitin-conjugating enzyme E3 ligase, and targets trichoplein, a keratin-binding protein, for degradation via polyubiquitinylation. A mutation in this gene is associated with autosomal dominant myoclonic dystonia 26.
Synonyms: FLJ12242
Cellular Location: Cytoplasm
Immunogen:
Recombinant protein of human KCTD17
Gene Symbol: KCTD17
Gene ID: 79734
Swiss prot: Q8N5Z5
Calculated MW: 36kDa
Recommended dilution:
IHC 1:50-200
Purity:
Affinity purification
Storage Buffer:
Buffer: PBS with 0.03% Proclin300, 50% glycerol, pH7.3.
Storage:
Store at -20℃. Avoid freeze / thaw cycles.
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