Mouse Anti-CAMK2A Recombinant Antibody (2C4) (CBMAB-C4785-LY)

Name: Mouse Anti-CAMK2A Recombinant Antibody (2C4)
SKU: CBMAB-C4785-LY
Rating: 5 (1 reviews)

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Datasheet

SDS

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Datasheet Target References Q & As Review & reward Protocols Associated Products

Basic Information

Host Animal

Mouse

Clone

2C4

Application

WB, ELISA, IF

Immunogen

CAMK2A (AAH40457, 305 a.a. ~ 410 a.a) partial recombinant protein with GST tag.

Host Species

Mouse

Specificity

Rat, Human

Antibody Isotype

IgG2a, κ

Clonality

Monoclonal

Application Notes

The COA includes recommended starting dilutions, optimal dilutions should be determined by the end user.

Application	Note
IF(ICC)	10 µg/ml

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

Format

Liquid

Buffer

PBS

Preservative

None

Concentration

Batch dependent

Purity

> 95% Purity determined by SDS-PAGE.

Storage

Store at +4°C short term (1-2 weeks). Aliquot and store at -20°C long term. Avoid repeated freezethaw cycles.

More Infomation

Target

Full Name

Calcium/Calmodulin Dependent Protein Kinase II Alpha

Introduction

CAMK2A (Calcium/Calmodulin Dependent Protein Kinase II Alpha) is a Protein Coding gene. Diseases associated with CAMK2A include Mental Retardation, Autosomal Dominant 53 and Alacrima, Achalasia, And Mental Retardation Syndrome. Among its related pathways are RET signaling and Salivary secretion. Gene Ontology (GO) annotations related to this gene include protein homodimerization activity and protein kinase activity.
An important paralog of this gene is CAMK2D.

Entrez Gene ID

Human	815
Rat	25400

UniProt ID

Human	Q9UQM7
Rat	P11275

Function

Calcium/calmodulin-dependent protein kinase that functions autonomously after Ca2+/calmodulin-binding and autophosphorylation, and is involved in synaptic plasticity, neurotransmitter release and long-term potentiation. Member of the NMDAR signaling complex in excitatory synapses, it regulates NMDAR-dependent potentiation of the AMPAR and therefore excitatory synaptic transmission (By similarity).
Regulates dendritic spine development (PubMed:28130356).
Also regulates the migration of developing neurons (PubMed:29100089).
Phosphorylates the transcription factor FOXO3 to activate its transcriptional activity (PubMed:23805378).
Acts as a negative regulator of 2-arachidonoylglycerol (2-AG)-mediated synaptic signaling via modulation of DAGLA activity (By similarity).

Biological Process

Angiotensin-activated signaling pathway Source: UniProtKB
Calcium ion transport Source: ParkinsonsUK-UCL
Dendritic spine development Source: UniProtKB
G1/S transition of mitotic cell cycle Source: ParkinsonsUK-UCL
Interferon-gamma-mediated signaling pathway Source: Reactome
MAPK cascade Source: Reactome
Negative regulation of hydrolase activity Source: UniProtKB
Peptidyl-serine phosphorylation Source: ParkinsonsUK-UCL
Peptidyl-threonine autophosphorylation Source: UniProtKB
Positive regulation of calcium ion transport Source: ParkinsonsUK-UCL
Positive regulation of cardiac muscle cell apoptotic process Source: ParkinsonsUK-UCL
Positive regulation of NF-kappaB transcription factor activity Source: UniProtKB
Protein autophosphorylation Source: ParkinsonsUK-UCL
Protein phosphorylation Source: UniProtKB
Regulation of cellular response to heat Source: Reactome
Regulation of endocannabinoid signaling pathway Source: UniProtKB
Regulation of mitochondrial membrane permeability involved in apoptotic process Source: ParkinsonsUK-UCL
Regulation of neuronal synaptic plasticity Source: ParkinsonsUK-UCL
Regulation of neuron migration Source: UniProtKB
Regulation of neurotransmitter secretion Source: ParkinsonsUK-UCL
Regulation of NMDA receptor activity Source: Reactome
Response to ischemia Source: ParkinsonsUK-UCL
Wnt signaling pathway, calcium modulating pathway Source: Reactome

Cellular Location

Synapse; Postsynaptic density; Dendritic spine; Dendrite. Postsynaptic lipid rafts.

Involvement in disease

Mental retardation, autosomal dominant 53 (MRD53): A form of mental retardation, a disorder characterized by significantly below average general intellectual functioning associated with impairments in adaptive behavior and manifested during the developmental period.
Mental retardation, autosomal recessive 63 (MRT63): A form of mental retardation, a disorder characterized by significantly below average general intellectual functioning associated with impairments in adaptive behavior and manifested during the developmental period. MRT63 patients manifest global developmental delay, severe intellectual disability, and seizures.

PTM

Autophosphorylation of Thr-286 following activation by Ca2+/calmodulin. Phosphorylation of Thr-286 locks the kinase into an activated state.
Palmitoylated. Probably palmitoylated by ZDHHC3 and ZDHHC7.

Bolton, S. C. (2019). Quaternary Structure Analysis of Calcium/Calmodulin-Dependent Protein Kinase II Alpha by Cryo-Electron Microscopy (Doctoral dissertation, Purdue University Graduate School).

Küry, S., van Woerden, G. M., Besnard, T., Onori, M. P., Latypova, X., Towne, M. C., ... & Mercier, S. (2017). De novo mutations in protein kinase genes CAMK2A and CAMK2B cause intellectual disability. The American Journal of Human Genetics, 101(5), 768-788.

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Please try the standard protocols which include: protocols, troubleshooting and guide.

Enzyme-linked Immunosorbent Assay (ELISA)
Flow Cytometry
Immunofluorescence (IF)
Immunohistochemistry (IHC)
Immunoprecipitation (IP)
Western Blot (WB)
Enzyme-Linked Immunospot (ELISpot)
Proteogenomics
Other Protocols

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Isotype control

For research use only. Not intended for any clinical use.

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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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