Full Product Name
IFT80 Rabbit Polyclonal
Product Gene Name
anti-IFT80 antibody
[Similar Products]
Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
Species Reactivity
Human, Mouse
Purity/Purification
>=95% as determined by SDS-PAGE
Immunogen Affinity Purified
Immunogen
Intraflagellar transport 80 homolog (Chlamydomonas)
Preparation and Storage
PBS with 0.02% sodium azide and 50% glycerol pH 7.3, -20 degree C for 24 months (Avoid repeated freeze / thaw cycles.)
ISO Certification
Manufactured in an ISO 13485:2003 and EN ISO 13485:2012 Certified Laboratory.
Other Notes
Small volumes of anti-IFT80 antibody vial(s) may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice and additional dry ice fee may apply.
Applications Tested/Suitable for anti-IFT80 antibody
ELISA (EIA), Western Blot (WB)
NCBI/Uniprot data below describe general gene information for IFT80. It may not necessarily be applicable to this product.
NCBI Accession #
NP_001177171.1
[Other Products]
NCBI GenBank Nucleotide #
NM_001190242.1
[Other Products]
UniProt Secondary Accession #
Q3MJC4; Q86YF4; Q9UIX1; B4E0K1; C9J8I0[Other Products]
UniProt Related Accession #
Q9P2H3[Other Products]
Molecular Weight
123,321 Da
NCBI Official Full Name
intraflagellar transport protein 80 homolog isoform b
NCBI Official Synonym Full Names
intraflagellar transport 80
NCBI Official Symbol
IFT80??[Similar Products]
NCBI Official Synonym Symbols
ATD2; SRTD2; WDR56
??[Similar Products]
NCBI Protein Information
intraflagellar transport protein 80 homolog
UniProt Protein Name
Intraflagellar transport protein 80 homolog
UniProt Synonym Protein Names
WD repeat-containing protein 56
Protein Family
Intraflagellar transport protein
UniProt Gene Name
IFT80??[Similar Products]
UniProt Synonym Gene Names
KIAA1374; WDR56??[Similar Products]
UniProt Entry Name
IFT80_HUMAN
NCBI Summary for IFT80
The protein encoded by this gene is part of the intraflagellar transport complex B and is necessary for the function of motile and sensory cilia. Defects in this gene are a cause of asphyxiating thoracic dystrophy 2 (ATD2). Three transcript variants encoding two different isoforms have been found for this gene.[provided by RefSeq, Jun 2010]
UniProt Comments for IFT80
IFT80: Component of the intraflagellar transport (IFT) complex B, which is essential for the development and maintenance of motile and sensory cilia. Defects in IFT80 are the cause of asphyxiating thoracic dystrophy type 2 (ATD2). An autosomal recessive chondrodysplasia characterized by a severely constricted thoracic cage, short-limbed short stature, and polydactyly. It often leads to death in infancy because of respiratory insufficiency. Retinal degeneration, cystic renal disease and hepatic disease can be present in affected individuals who survive early childhood.
Chromosomal Location of Human Ortholog: 3q25.33
Cellular Component: centrosome; cilium; cytoplasm
Biological Process: chondrocyte differentiation; cilium biogenesis; negative regulation of epithelial cell proliferation; osteoblast differentiation; positive regulation of smoothened signaling pathway; sensory cilium biogenesis; smoothened signaling pathway
Disease: Short-rib Thoracic Dysplasia 2 With Or Without Polydactyly
Research Articles on IFT80
1. Mutations in IFT80 can be responsible for a lethal form of short-rib polydactyly and provide the molecular basis for the Jeune-Verma-Naumoff dysplasia spectrum.
Precautions
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Disclaimer
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