Anti-CNTNAP1 Antibody

$99.00$319.00

Reactivity: Human
Applications: ELISA,IHC
Conjugation: Various
Supplier: CUSABIO BIOTECH CO.

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Rabbit Anti-CNTNAP1 Antibody (CSB-PA005692ESR1HU)

Supplier: CUSABIO BIOTECH CO.

Alternative names:

Contactin-associated protein 1 Antibody,Caspr Antibody,Caspr1 Antibody,Neurexin IV Antibody,Neurexin-4 Antibody,p190 Antibody,CNTNAP1 Antibody,CASPR Antibody,NRXN4 Antibody

More alternative names for the antibody
Caspr antibody|Caspr1 antibody|CNTNAP antibody|Cntnap1 antibody|CNTP1_HUMAN antibody|Contactin associated protein 1 antibody|Contactin-associated protein 1 antibody|MHDNIV antibody|NCP1 antibody|Neurexin 4 antibody|Neurexin IV antibody|Neurexin-4 antibody|Nrxn4 antibody|p190 antibody|Paranodin antibody
Anti-Caspr antibody (ab34151)
Close sc-374489|sc-373777|sc-25669|sc-11174|sc-14340|sc-23273|

Recommended applications: ELISA, IHC

Recommended dilution: Recommended dilution:IHC:1:20-1:200

Recommended protocols: check protocols

Name

Anti-CNTNAP1 Antibody

Catalogue No.

CSB-PA005692ESR1HU

Reactivity

Human

Immunogen

Recombinant human Contactin-associated protein 1 protein (20-300AA)

Host

Rabbit

Applications

ELISA, IHC

Recommended dilution

Recommended dilution:IHC:1:20-1:200

Clonality

Polyclonal

Conjugation

unconjugated

Isotype

IgG

Molecular weight

156 kDa

Purification

Antigen Affinity Purified

Storage

Shipped at 4 Celcius Degree. Upon delivery aliquot and store at -20 Celcius Degree or -80 Celcius Degree. Avoid repeated freeze.

Database links

Entrez Gene:8506( Human), Entrez Gene:53321( Mouse), Entrez Gene:84008( Rat), Omim:602346( Human), SwissProt:P78357( Human), SwissProt:O54991( Mouse), SwissProt:P97846( Rat), Unigene:408730( Human), Unigene:474527( Mouse), Unigene:88654( Rat)

Protein function

Seems to play a role in the formation of functional distinct domains critical for saltatory conduction of nerve impulses in myelinated nerve fibers. Seems to demarcate the paranodal region of the axo-glial junction. In association with contactin may have a role in the signaling between axons and myelinating glial cells.

Protein tissue specificity

Predominantly expressed in brain. Weak expression detected in ovary, pancreas, colon, lung, heart, intestine and testis.

Involvement in disease

Lethal congenital contracture syndrome 7 (LCCS7) [MIM:616286]: A form of lethal congenital contracture syndrome, an autosomal recessive disorder characterized by degeneration of anterior horn neurons, extreme skeletal muscle atrophy and congenital non-progressive joint contractures. The contractures can involve the upper or lower limbs and/or the vertebral column, leading to various degrees of flexion or extension limitations evident at birth. LCCS7 is a severe axoglial disease characterized by congenital distal joint contractures, polyhydramnios, reduced fetal movements, and motor paralysis leading to death early in the neonatal period. . Note=The disease is caused by mutations affecting the gene represented in this entry.

Protein sequence and domain

Belongs to the neurexin family.

Protein cellular localization

Membrane ; Single-pass type I membrane protein .

Research area

All research areas>Neurobiology Antibodies>CASPR
(View all antibody categories related to Neurobiology Antibodies)

Note

AntibodyPlus provides antibody trial sample for your own antibody validation and collects antibody reviews.

Supplier

CUSABIO BIOTECH CO.

Product type

Primary antibody

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