CELSR1 Antibodies

AND CELSR1 ELISA kits, CELSR1 Proteins

Many biological assays use antibodies to detect CELSR1, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with CELSR1 in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop CELSR1 antibodies...

We validate the specificity of these antibodies to CELSR1 by testing them on tissues known to express CELSR1 positively and negatively. Browse below to find the CELSR1 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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CELSR1 Infographic by Boster Bio

All CELSR1 Products

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Anti-CELSR1 Antibody

1 Q&As

Human, Mouse, Rat

ELISA, IF, ICC

$335
Cat # A06056-1
100ul

CELSR1 Overview

Facts about Cadherin EGF LAG seven-pass G-type receptor 1.

Cadherin EGF LAG seven-pass G-type receptor 1 (CELSR1)

Receptor that may have an important role in cell/cell signaling during nervous system formation. .

Gene Information

Human
Gene Name:	CELSR1
Uniprot:	Q9NYQ6
Entrez:	9620

Family

Belongs to:

G-protein coupled receptor 2 family

Alternative Names

cadherin, EGF LAG seven-pass G-type receptor 1 (flamingo homolog, Drosophila); DKFZp434P0729; flamingo homolog 2; FMI2; HFMI2; ME2; protocadherin flamingo 2

Molecular Weight

Mass (kDA):
329.486 kDA

Genomic Context


Human

Location:	22q13.31
Sequence:	22; NC_000022.11 (46361174..46537620, complement)

Subcellular Localizations

Cell membrane; Multi-pass membrane protein.

Diseases

Congenital Abnormality
Neoplasms
Tissue Adhesions
Strabismus
Carcinoma
Malignant Neoplasms
Nervousness
Cell Invasion
Brain Ischemia
Malignant Neoplasm Of Breast
Dysequilibrium Syndrome
Anencephaly

Spina Bifida
Malignant Neoplasm Of Lung
Carcinogenesis
Cerebrovascular Accident
Colorectal Cancer
Ischemic Stroke
Schizophrenia

Pathways

Neural Tube Closure
Tube Closure
Localization
Gastrulation
Convergent Extension
Cell Adhesion
Lung Development
Cell Division
Initiation Of Neural Tube Closure
Mitosis
Pathogenesis
Dorsal Convergence
Tube Formation

Neurogenesis
Spermatogenesis
Pronephros Development
Apical Constriction
Cytoskeleton Organization
Cell Cycle
Cell Motility

PTMs

Phosphorylation

Methylation

Research Areas

GPCR

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/CELSR1

References

PMID: 10716726 by Wu Q., et al. Large exons encoding multiple ectodomains are a characteristic feature of protocadherin genes.

PMID: 22095531 by Robinson A., et al. Mutations in the planar cell polarity genes CELSR1 and SCRIB are associated with the severe neural tube defect craniorachischisis.