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Product Name
TCTN3 antibody
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Description
TCTN3 Rabbit Polyclonal antibody. Positive IP detected in Hela cells. Positive WB detected in Transfected HEK-293 cells. Positive IHC detected in human lung tissue. Positive IF detected in hTERT-RPE1 cells.
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Tested applications
ELISA, IHC, IF, IP, WB
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Species reactivity
Human; other species not tested.
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Alternative names
C10orf61 antibody; DKFZp564D116 antibody; TCTN3 antibody; TECT3 antibody; Tectonic 3 antibody; tectonic family member 3 antibody; UNQ1881/PRO4324 antibody
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Isotype
Rabbit IgG
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Preparation
This antibody was obtained by immunization of TCTN3 recombinant protein (Accession Number: BC009494). Purification method: Antigen affinity purified.
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Clonality
Polyclonal
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Formulation
PBS with 0.02% sodium azide and 50% glycerol pH 7.3.
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Storage instructions
Store at -20℃. DO NOT ALIQUOT
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Applications
Recommended Dilution:
WB: 1:500-1:5000
IP: 1:200-1:2000
IHC: 1:20-1:200
IF: 1:20-1:200
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Validations
IP result of anti-TCTN3(Catalog No:115921 for IP and Detection).
Immunohistochemical of paraffin-embedded human lung using Catalog No:115921(TCTN3 antibody) at dilution of 1:50 (under 40x lens)
IF result from Dr. Corbit, Kevin. anti-TCTN3(Catalog No:115921) mark the transition zone of Human hTERT-RPE1 cells.
Transfected HEK-293 cells were subjected to SDS PAGE followed by western blot with Catalog No:115921(TCTN3 Antibody) at dilution of 1:1000
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Background
TCTN3 (tectonic-3 or TECT3) is a type I membrane protein that belongs to the tectonic family, which consists of TCTN1, TCTN2 and TCTN3. Studies in mice suggest that tectonic may be involved in Hedgehog (Hh) signaling, and essential for ciliogenesis. Tectonic is 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. TCTN3 is necessary for transduction of the sonic hedgehog (SHH) signaling pathway. Orofaciodigital syndromes (OFDSs) consist of a group of heterogeneous disorders characterized by abnormalities in the oral cavity, face, and digits and associated phenotypic abnormalities. Recently, TCTN3 mutations are found as the cause of an extreme form of OFD associated with bone dysplasia, tibial defect, cystic kidneys, and brain anomalies.
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References
- Garcia-Gonzalo FR, Corbit KC, Sirerol-Piquer MS. A transition zone complex regulates mammalian ciliogenesis and ciliary membrane composition. Nature genetics. 43(8):776-84. 2011.
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