C20orf194 Antibodies

AND C20orf194 ELISA kits, C20orf194 Proteins

Many biological assays use antibodies to detect C20orf194, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with C20orf194 in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop C20orf194 antibodies...

We validate the specificity of these antibodies to C20orf194 by testing them on tissues known to express C20orf194 positively and negatively. Browse below to find the C20orf194 antibody that suites your experiment. We have 1 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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C20orf194 Infographic by Boster Bio

All C20orf194 Products

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DNAAF9 (NM_001009984) Human Over-expression Lysate

Human

$960
Cat # LS025943
20 µg, 100 µg

C20orf194 Overview

Facts about Uncharacterized protein C20orf194.

C20orf194 3D structure. Source: alphafold

Uncharacterized protein C20orf194 (C20orf194)

May act as an effector for ARL3.
.

Gene Information

Human
Gene Name:	C20orf194
Uniprot:	Q5TEA3
Entrez:	25943

Family

Belongs to:

No superfamily

Alternative Names

C20orf194 chromosome 20 open reading frame 194

Molecular Weight

Mass (kDA):
132.287 kDA

Genomic Context


Human

Location:	20p13
Sequence:	20; NC_000020.11 (3249302..3407662, complement)

Diseases

Sclerosis
Primary Lateral Sclerosis
Neurodegenerative Disorders
Ataxia
Alzheimer's Disease
Ataxia, Spinocerebellar

Amyotrophic Lateral Sclerosis

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/C20orf194

References

PMID: 22085962 by Wright K.J., et al. An ARL3-UNC119-RP2 GTPase cycle targets myristoylated NPHP3 to the primary cilium.

PMID: 21683323 by Kobayashi H., et al. Expansion of intronic GGCCTG hexanucleotide repeat in NOP56 causes SCA36, a type of spinocerebellar ataxia accompanied by motor neuron involvement.