Complexin-3 Antibodies

AND Cplx3 ELISA kits, Complexin-3 Proteins

Many biological assays use antibodies to detect Complexin-3, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with Complexin-3 in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop Complexin-3 antibodies...

We validate the specificity of these antibodies to Complexin-3 by testing them on tissues known to express Cplx3 positively and negatively. Browse below to find the Cplx3 antibody that suites your experiment. We have 2 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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Cplx3 Infographic by Boster Bio

All Cplx3 Products

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Specificity

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Price

CPLX3 (NM_001030005) Human Recombinant Protein

$813
Cat # PROTQ8WVH0
20 µg

CPLX3 (NM_001030005) Human Over-expression Lysate

Human

$628
Cat # LS594855
100 µg

Cplx3 Overview

Facts about Complexin-3.

Complexin-3 (Cplx3)

Positively regulates a late step in synaptic vesicle exocytosis. .

Gene Information

Mouse
Gene Name:	Cplx3
Uniprot:	Q8R1B5
Entrez:	235415

Family

Belongs to:

complexin/synaphin family

Alternative Names

complexin 3; Complexin III; complexin-3; CPX III; CPXIII; CPX-III; DKFZp434E1719; FLJ00167; FLJ00250; FLJ13993

Molecular Weight

Mass (kDA):
17.586 kDA

Genomic Context


Mouse

Location:	9\|9 B
Sequence:	9;

Tissue Specificity

Present in many brain regions, including hippocampus and cerebellum. In the retina, present both at conventional amacrine cell synapses and at photoreceptor ribbon synapses (at protein level).

Diseases

Somatotropin Deficiency
Malnutrition
Atresia
Orbital Separation Excessive
Digeorge Syndrome
Nervousness
Prader-willi Syndrome
Congenital Diaphragmatic Hernia
Infective Disorder
Meningomyelocele
Anus, Imperforate

Noonan Syndrome
Congenital Abnormality
Intestinal Atresia
Muscle Hypotonia
Developmental Disabilities
Hernia

Pathways

Synaptic Vesicle Fusion
Vesicle Fusion
Exocytosis
Synaptic Vesicle Exocytosis
Signal Transmission

PTMs

Lipoprotein

Methylation

Prenylation

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/Cplx3

References

PMID: 15911881 by Reim K., et al. Structurally and functionally unique complexins at retinal ribbon synapses.

PMID: 19386896 by Reim K., et al. Aberrant function and structure of retinal ribbon synapses in the absence of complexin 3 and complexin 4.