PEX16 Antibodies

AND PEX16 ELISA kits, PEX16 Proteins

Many biological assays use antibodies to detect PEX16, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with PEX16 in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop PEX16 antibodies...

We validate the specificity of these antibodies to PEX16 by testing them on tissues known to express PEX16 positively and negatively. Browse below to find the PEX16 antibody that suites your experiment. We have 3 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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PEX16 Infographic by Boster Bio

All PEX16 Products

Filter by Application:

Product

Figures

Specificity

Applications

Price

Anti-PEX16 Antibody

Human, Mouse

ELISA, WB

$380
Cat # A06382
100ul

PEX16 (NM_004813) Human Recombinant Protein

$813
Cat # PROTQ9Y5Y5
20 µg

PEX16 (NM_004813) Human Over-expression Lysate

Human

$628
Cat # LS009409
100 µg

PEX16 Overview

Facts about Peroxisomal membrane protein PEX16.

PEX16 3D structure. Source: alphafold

Peroxisomal membrane protein PEX16 (PEX16)

Required for peroxisome membrane biogenesis. May play a role in early stages of peroxisome assembly.

Can recruit other peroxisomal proteins, such as PEX3 and PMP34, to de novo peroxisomes derived from the endoplasmic reticulum (ER). May function as receptor for PEX3.

Gene Information

Human
Gene Name:	PEX16
Uniprot:	Q9Y5Y5
Entrez:	9409

Family

Belongs to:

peroxin-16 family

Alternative Names

peroxin-16; peroxisomal biogenesis factor 16peroxin 16; peroxisomal membrane protein PEX16; peroxisome biogenesis factor 16

Molecular Weight

Mass (kDA):
38.629 kDA

Genomic Context


Human

Location:	11p11.2
Sequence:	11; NC_000011.10 (45909663..45918123, complement)

Subcellular Localizations

Peroxisome membrane; Multi-pass membrane protein.

Diseases

Zellweger Syndrome
Disorders Of Peroxisome Biogenesis
Peroxisomal Disorders
Muscle Hypotonia
Chondrodysplasia Punctata
Inborn Errors Of Metabolism
Ataxia
Neuronal Migration Disorders
Paraparesis
Refsum Disease

Cerebrovascular Accident
Chondrodysplasia Punctata, Rhizomelic
Potocki-shaffer Syndrome
Chronic Fatigue Syndrome
Hereditary Diseases

Interacting Proteins

PEX19

Pathways

Membrane Biogenesis
Protein Import
Localization
Transport
Membrane Assembly
Protein Secretion
Translation
Pathogenesis
Secretion
Cell Activation
Protein Targeting
T Cell Activation
Proteolysis

Membrane Fission
Organelle Localization
Secretory Pathway
Vesicle Transport
Peroxisome Fission
Glycosylation
Fatty Acid Beta-oxidation

PTMs

Glycosylation

Oxidation

Prenylation

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/PEX16

References

PMID: 9837814 by Honsho M., et al. Mutation in PEX16 is causal in the peroxisome-deficient Zellweger syndrome of complementation group D.

PMID: 9922452 by South S.T., et al. Peroxisome synthesis in the absence of preexisting peroxisomes.