IFT80 Antibodies

AND IFT80 ELISA kits, IFT80 Proteins

Many biological assays use antibodies to detect IFT80, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with IFT80 in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop IFT80 antibodies...

We validate the specificity of these antibodies to IFT80 by testing them on tissues known to express IFT80 positively and negatively. Browse below to find the IFT80 antibody that suites your experiment. We have 0 of these antibodies and many publications and validation images.

If you cannot find antibodies that fit your needs, contact us for making custom antibodies. We have a full suite of custom antibody services covering from research to diagnostic and therapeutic applications.

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IFT80 Infographic by Boster Bio

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IFT80 Overview

Facts about Intraflagellar transport protein 80 homolog.

IFT80 3D structure. Source: alphafold

Intraflagellar transport protein 80 homolog (IFT80)

Component of the intraflagellar transport (IFT) complex B, which is essential for the development and maintenance of motile and sensory cilia. .

Gene Information

Human
Gene Name:	IFT80
Uniprot:	Q9P2H3
Entrez:	57560

Family

Belongs to:

No superfamily

Alternative Names

ATD2; intraflagellar transport 80 homolog (Chlamydomonas); intraflagellar transport protein 80 homolog; KIAA1374WDR56WD repeat domain 56; MGC126543; WD repeat-containing protein 56

Molecular Weight

Mass (kDA):
88.035 kDA

Genomic Context


Human

Location:	3q25.33
Sequence:	3; NC_000003.12 (160256986..160399225, complement)

Tissue Specificity

Isoform IFT80-L is widely expressed.

Subcellular Localizations

Cytoplasm. Cytoplasm, cytoskeleton, cilium basal body. Cytoplasm, cytoskeleton, cilium axoneme. Basal body and ciliary axoneme.

Diseases

Jeune Thoracic Dystrophy
Dystrophy
Polydactyly
Short Rib-polydactyly Syndrome
Retinal Degeneration
Asphyxia
Thoracic Diseases
Cystic Kidney Diseases
Kidney Diseases
Ellis-van Creveld Syndrome
Stenosis

Dysostoses
Congenital Anomaly Of Face
Dysplasia
Micromelia
Situs Inversus

Pathways

Transport
Intraflagellar Transport
Swimming
Cell Proliferation
Osteoblast Differentiation
Cell Cycle
Cell Differentiation

Localization
Rna Interference

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/IFT80

References

PMID: 17468754 by Beales P.L., et al. IFT80, which encodes a conserved intraflagellar transport protein, is mutated in Jeune asphyxiating thoracic dystrophy.

PMID: 18601909 by Huang W., et al. Identification and characterization of a long isoform of human IFT80, IFT80-L.