Protein KIAA0556 Antibodies

AND KIAA0556 ELISA kits, Protein KIAA0556 Proteins

Many biological assays use antibodies to detect Protein KIAA0556, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with Protein KIAA0556 in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop Protein KIAA0556 antibodies...

We validate the specificity of these antibodies to Protein KIAA0556 by testing them on tissues known to express KIAA0556 positively and negatively. Browse below to find the KIAA0556 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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KIAA0556 Infographic by Boster Bio

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KIAA0556 Overview

Facts about Protein KIAA0556.

KIAA0556 3D structure. Source: alphafold

Protein KIAA0556 (KIAA0556)

May influence the stability of microtubules (MT), possibly through interaction with the MT-severing katanin complicated. .

Gene Information

Human
Gene Name:	KIAA0556
Uniprot:	O60303
Entrez:	23247

Family

Belongs to:

No superfamily

Alternative Names

hypothetical protein LOC23247; KIAA0556

Molecular Weight

Mass (kDA):
180.918 kDA

Genomic Context


Human

Location:	16p12.1
Sequence:	16; NC_000016.10 (27550128..27780371)

Subcellular Localizations

Cytoplasm, cytoskeleton, cilium axoneme. Cytoplasm, cytoskeleton, cilium basal body. Cytoplasm, cytoskeleton. When overexpressed, localizes to the cytoplasm where it associates with acetylated alpha-tubulin.

Diseases

Chromosome Break

PTMs

Phosphoprotein

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/KIAA0556

References

PMID: 26714646 by Sanders A.A., et al. KIAA0556 is a novel ciliary basal body component mutated in Joubert syndrome.

PMID: 30237576 by Maddirevula S., et al. Autozygome and high throughput confirmation of disease genes candidacy.