Anti-CHN1 Antibody

$99.00$319.00

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

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Rabbit Anti-CHN1 Antibody (CSB-PA005368ESR1HU)

Supplier: CUSABIO BIOTECH CO.

Alternative names:

N-chimaerin Antibody,A-chimaerin Antibody,Alpha-chimerin Antibody,N-chimerin Antibody,NC Antibody,Rho GTPase-activating protein 2 Antibody,CHN1 Antibody,ARHGAP2 Antibody,CHN Antibody

More alternative names for the antibody
A-chimaerin antibody|Alpha-chimerin antibody|ARHGAP2 antibody|CHIN_HUMAN antibody|CHN antibody|Chn1 antibody|N chimaerin antibody|N chimerin antibody|N-chimaerin antibody|N-chimerin antibody|NC antibody|Rho GTPase-activating protein 2 antibody|RHOGAP2 antibody
Anti-CHN 1 antibody [2G6] (ab131590)
Close sc-365985|

Recommended applications: ELISA, WB, IHC

Recommended dilution: User optimized

Recommended protocols: check protocols

Name

Anti-CHN1 Antibody

Catalogue No.

CSB-PA005368ESR1HU

Reactivity

Human

Immunogen

Recombinant human N-chimaerin protein (1-200AA)

Host

Rabbit

Applications

ELISA, WB, IHC

Recommended dilution

User optimized

Clonality

Polyclonal

Conjugation

unconjugated

Isotype

IgG

Molecular weight

53 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:1123( Human), Omim:118423( Human), SwissProt:P15882( Human), Unigene:380138( Human)

Protein function

GTPase-activating protein for p21-rac and a phorbol ester receptor. Involved in the assembly of neuronal locomotor circuits as a direct effector of EPHA4 in axon guidance.

Protein tissue specificity

In neurons in brain regions that are involved in learning and memory processes.

Involvement in disease

Duane retraction syndrome 2 (DURS2) [MIM:604356]: A form of Duane retraction syndrome, a congenital eye movement disorder characterized by a failure of cranial nerve VI (the abducens nerve) to develop normally, resulting in restriction or absence of abduction, adduction or both, narrowing of the palpebral fissure, and retraction of the globe on attempted adduction. Undiagnosed in children, it can lead to amblyopia, a permanent uncorrectable loss of vision. . Note=The disease is caused by mutations affecting the gene represented in this entry.

Protein post-translational modifications

Phosphorylated. Phosphorylation is EPHA4 kinase activity-dependent (By similarity). .

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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