WDR60 Antibodies

AND WDR60 ELISA kits, WDR60 Proteins

Many biological assays use antibodies to detect WDR60, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with WDR60 in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop WDR60 antibodies...

We validate the specificity of these antibodies to WDR60 by testing them on tissues known to express WDR60 positively and negatively. Browse below to find the WDR60 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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WDR60 Infographic by Boster Bio

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WDR60 Overview

Facts about WD repeat-containing protein 60.

WDR60 3D structure. Source: alphafold

WD repeat-containing protein 60 (WDR60)

May play a role in ciliogenesis. .

Gene Information

Human
Gene Name:	WDR60
Uniprot:	Q8WVS4
Entrez:	55112

Family

Belongs to:

No superfamily

Alternative Names

FLJ10300; FLJ23575; WD repeat domain 60; WD repeat-containing protein 60

Molecular Weight

Mass (kDA):
122.571 kDA

Genomic Context


Human

Location:	7q36.3
Sequence:	7; NC_000007.14 (158839245..158958695)

Tissue Specificity

Expressed in chondrocytes (at protein level).

Subcellular Localizations

Cell projection, cilium. Located at the base of the primary cilium in serum-starved fibroblasts.

Diseases

Hoarseness
Developmental Delay (disorder)
Neurofibromatosis 1
Neurofibromatoses
Trisomy
Unbalanced Translocation

Interacting Proteins

NUDC

PTMs

Phosphoprotein

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/WDR60

References

PMID: 25492405 by McInerney-Leo A.M., et al. Whole exome sequencing is an efficient, sensitive and specific method for determining the genetic cause of short-rib thoracic dystrophies.

PMID: 26044572 by Schmidts M., et al. TCTEX1D2 mutations underlie Jeune asphyxiating thoracic dystrophy with impaired retrograde intraflagellar transport.