Sorting nexin-14 Antibodies

AND SNX14 ELISA kits, Sorting nexin-14 Proteins

Many biological assays use antibodies to detect Sorting nexin-14, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with Sorting nexin-14 in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop Sorting nexin-14 antibodies...

We validate the specificity of these antibodies to Sorting nexin-14 by testing them on tissues known to express SNX14 positively and negatively. Browse below to find the SNX14 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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SNX14 Infographic by Boster Bio

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SNX14 Overview

Facts about Sorting nexin-14.

SNX14 3D structure. Source: alphafold

Sorting nexin-14 (SNX14)

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Gene Information

Human
Gene Name:	SNX14
Uniprot:	Q9Y5W7
Entrez:	57231

Family

Belongs to:

sorting nexin family

Alternative Names

MGC13217; RGS-PX2; sorting nexin 14; sorting nexin-14

Molecular Weight

Mass (kDA):
110.182 kDA

Genomic Context


Human

Location:	6q14.3
Sequence:	6; NC_000006.12 (85505496..85594156, complement)

Tissue Specificity

Widely expressed both in fetal and adult tissues.

Subcellular Localizations

Lysosome membrane; Multi-pass membrane protein. Late endosome membrane; Multi-pass membrane protein. Cell projection, dendrite.

Diseases

Neuroblastoma
Nervousness
Developmental Delay (disorder)
Bipolar Disorder

PTMs

Phosphoprotein

Research Areas

Signal Transduction

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/SNX14

References

PMID: 11485546 by Teasdale R.D., et al. A large family of endosome-localized proteins related to sorting nexin 1.

PMID: 25439728 by Thomas A.C., et al. Mutations in SNX14 cause a distinctive autosomal-recessive cerebellar ataxia and intellectual disability syndrome.