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Mouse Anti-NTNG2 Recombinant Antibody (4F11) (CBMAB-N0553-WJ)

This product is a Mouse antibody that recognizes NTNG2. The antibody 4F11 can be used for immunoassay techniques such as: ELISA, WB, IHC.
See all NTNG2 antibodies

Summary

Host Animal
Mouse
Specificity
Human
Clone
4F11
Antibody Isotype
IgG2b, κ
Application
ELISA, WB, IHC

Basic Information

Specificity
Human
Antibody Isotype
IgG2b, κ
Clonality
Monoclonal
Application Notes
The COA includes recommended starting dilutions, optimal dilutions should be determined by the end user.

Formulations & Storage [For reference only, actual COA shall prevail!]

Format
Liquid
Buffer
PBS, pH 7.2
Storage
Store at +4°C short term (1-2 weeks). Aliquot and store at -20°C long term. Avoid repeated freeze/thaw cycles.

Target

Full Name
netrin G2
Introduction
Involved in controlling patterning and neuronal circuit formation at the laminar, cellular, subcellular and synaptic levels. Promotes neurite outgrowth of both axons and dendrites.
Entrez Gene ID
84628
UniProt ID
Q96CW9
Alternative Names
Netrin G2; Netrin G1; Netrin-G2; Lmnt2; BA479K20.1 (Novel Protein); BA479K20.1;
Function
Involved in controlling patterning and neuronal circuit formation at the laminar, cellular, subcellular and synaptic levels. Promotes neurite outgrowth of both axons and dendrites.
Biological Process
Animal organ morphogenesisManual Assertion Based On ExperimentIBA:GO_Central
AxonogenesisISS:UniProtKB
Basement membrane assemblyManual Assertion Based On ExperimentIBA:GO_Central
Cell migrationManual Assertion Based On ExperimentIBA:GO_Central
Modulation of chemical synaptic transmissionIEA:Ensembl
Postsynaptic specialization assemblyIEA:Ensembl
Regulation of neuron migrationISS:UniProtKB
Regulation of neuron projection arborizationISS:UniProtKB
Regulation of neuron projection developmentISS:UniProtKB
Regulation of presynapse assemblyIEA:Ensembl
Substrate adhesion-dependent cell spreadingManual Assertion Based On ExperimentIBA:GO_Central
Synaptic membrane adhesionIEA:Ensembl
Tissue developmentManual Assertion Based On ExperimentIBA:GO_Central
Cellular Location
Cell membrane
Involvement in disease
Neurodevelopmental disorder with behavioral abnormalities, absent speech, and hypotonia (NEDBASH):
An autosomal recessive disorder characterized by global developmental delay with severely impaired intellectual development, impaired motor development, axial and peripheral hypotonia, poor speech and significant behavioral abnormalities, including autism spectrum disorder, hyperactivity, mood disorders, aggression, hand and face stereotypies, sleep disturbances, anxiety, self-injurious behavior, and bruxism.
PTM
N-glycosylated.
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For research use only. Not intended for any clinical use.

Custom Antibody Labeling

We also offer labeled antibodies developed using our catalog antibody products and nonfluorescent conjugates (HRP, AP, Biotin, etc.) or fluorescent conjugates (Alexa Fluor, FITC, TRITC, Rhodamine, Texas Red, R-PE, APC, Qdot Probes, Pacific Dyes, etc.).

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