WDR35 Antibodies

AND WDR35 ELISA kits, WDR35 Proteins

Many biological assays use antibodies to detect WDR35, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with WDR35 in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop WDR35 antibodies...

We validate the specificity of these antibodies to WDR35 by testing them on tissues known to express WDR35 positively and negatively. Browse below to find the WDR35 antibody that suites your experiment. We have 2 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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WDR35 Infographic by Boster Bio

All WDR35 Products

Product

Figures

Specificity

Applications

Price

Anti-WDR35 Antibody

Human

ELISA, IHC-P

$449
Cat # A07256
0.1 mg

WDR35 (NM_020779) Human Over-expression Lysate

Human

$628
Cat # LS057539
100 µg

WDR35 Overview

Facts about WD repeat-containing protein 35.

WDR35 3D structure. Source: alphafold

WD repeat-containing protein 35 (WDR35)

As a component of the IFT complex A (IFT-A), a complex required for retrograde ciliary transport, it is involved in ciliogenesis (PubMed:21473986, PubMed:28400947). May promote CASP3 activation and TNF-stimulated apoptosis.

Gene Information

Human
Gene Name:	WDR35
Uniprot:	Q9P2L0
Entrez:	57539

Family

Belongs to:

No superfamily

Alternative Names

CED2; IFT121; WD repeat domain 35

Molecular Weight

Mass (kDA):
133.547 kDA

Genomic Context


Human

Location:	2p24.1
Sequence:	2; NC_000002.12 (19910260..19990105, complement)

Subcellular Localizations

Cytoplasm, cytoskeleton, microtubule organizing center, centrosome. Cytoplasm, cytoskeleton, cilium axoneme. Cytoplasm, cytoskeleton, cilium basal body.

Diseases

Polydactyly
Dysplasia
Fibrosis
Short Rib-polydactyly Syndrome
Ectodermal Dysplasia
Hepatic Fibrosis
Cranioectodermal Dysplasia
Craniofacial Abnormalities
Dysostoses
Coronary Artery Disease
Congenital Anomaly Of Face
Congenital Heart Defects

Craniosynostosis
Micromelia
Dwarfism
Curry-hall Syndrome
L1 Acute Lymphoblastic Leukemia
Cleft Lip

Pathways

Transport
Intraflagellar Transport
Methylation
Translation
Dna Methylation
Pathogenesis

PTMs

Glycosylation

Methylation

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/WDR35

References

PMID: 19450523 by Cole D.G., et al. SnapShot: Intraflagellar transport.

PMID: 20193664 by Feng G.G., et al. Naofen, a novel WD40-repeat protein, mediates spontaneous and tumor necrosis factor-induced apoptosis.