Protein FAM161A Antibodies

AND Fam161a ELISA kits, Protein FAM161A Proteins

Many biological assays use antibodies to detect Protein FAM161A, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with Protein FAM161A in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop Protein FAM161A antibodies...

We validate the specificity of these antibodies to Protein FAM161A by testing them on tissues known to express Fam161a positively and negatively. Browse below to find the Fam161a 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.

Previous: Septin9 Next: Arhgap18

Fam161a Infographic by Boster Bio

All Fam161a Products

Product

Figures

Specificity

Applications

Price

Fam161a Overview

Facts about Protein FAM161A.

Protein FAM161A (Fam161a)

Involved in ciliogenesis.
.

Gene Information

Mouse
Gene Name:	Fam161a
Uniprot:	Q8QZV6
Entrez:	73873

Family

Belongs to:

FAM161 family

Alternative Names

family with sequence similarity 161, member A; RP28

Molecular Weight

Mass (kDA):
52.029 kDA

Genomic Context


Mouse

Location:	11\|11 A3.2
Sequence:	11;

Tissue Specificity

Expressed in the retina.

Diseases

Retinitis Pigmentosa
Retinal Degeneration
Abnormal Degeneration
Degenerative Disorder
Stenosis
Legal Blindness
Blind Vision

Pallor

Pathways

Transport
Mitosis
Pigmentation
Interphase
Pathogenesis
Localization

PTMs

Acetylation

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/Fam161a

References

PMID: 20705278 by Langmann T., et al. Nonsense mutations in FAM161A cause RP28-associated recessive retinitis pigmentosa.

PMID: 20705279 by Bandah-Rozenfeld D., et al. Homozygosity mapping reveals null mutations in FAM161A as a cause of autosomal-recessive retinitis pigmentosa.