Rabbit Polyclonal Phospho-NMDAepsilon2 (Y1474) antibody (STJ90823)

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Reactivity: Human, Mouse, Rat
Applications: WB, IHC, ELISA
Conjugation: Unconjugated
Supplier: St John’s Laboratory Ltd.

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Rabbit Polyclonal Phospho-NMDAepsilon2 (Y1474) antibody (STJ90823)

Supplier: St John’s Laboratory Ltd.

Recommended applications: WB, IHC, ELISA

Recommended dilution: WB 1:500-1:2000; IHC 1:100-1:300; ELISA 1:5000;

Recommended protocols: check protocols

Image descriptions:

Click or hover above images to see image description for NMDAepsilon2 (phospho Tyr1474) Polyclonal Antibody.

Alternative names:

Check alternative names for the antibody

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GRIN2B antibody, NMDAR2B antibody,|AW490526 antibody|EIEE27 antibody|Glutamate [NMDA] receptor subunit epsilon 2 antibody|Glutamate [NMDA] receptor subunit epsilon-2 antibody|Glutamate Receptor Ionotropic N Methyl D Aspartate 2B antibody|Glutamate Receptor Ionotropic N Methyl D Aspartate subunit 2B antibody|Glutamate receptor ionotropic NMDA2B antibody|Glutamate receptor subunit epsilon 2 antibody|Glutamate receptor, ionotropic, NMDA2B (epsilon 2) antibody|GRIN 2B antibody|GRIN2B antibody|hNR 3 antibody|hNR3 antibody|MGC142178 antibody|MGC142180 antibody|MRD6 antibody|N methyl D asparate receptor channel subunit epsilon 2 antibody|N methyl D aspartate receptor subtype 2B antibody|N methyl D aspartate receptor subunit 2B antibody|N methyl D aspartate receptor subunit 3 antibody|N-methyl D-aspartate receptor subtype 2B antibody|N-methyl-D-aspartate receptor subunit 3 antibody|NMDA NR2B antibody|NMDA R2B antibody|NMDAR2B antibody|NMDE2 antibody|NMDE2_HUMAN antibody|NME2 antibody|NR2B antibody|NR3 antibody|Anti-NMDAR2B antibody (ab65783)
SCBT cat No: sc-365597|sc-1469|sc-31545|sc-9057|sc-31543|sc-1470|

 

Name

NMDAepsilon2 (phospho Tyr1474) Polyclonal Antibody

Catalogue No.

STJ90823

Reactivity

Human, Mouse, Rat

Specificity

Phospho-NMDAepsilon2 (Y1474) Polyclonal Antibody detects endogenous levels of NMDAepsilon2 protein only when phosphorylated at Y1474.

Immunogen

Synthesized phospho-peptide derived from NMDAepsilon2 (phospho Tyr1474) at AA range 1410-1490

Host

Rabbit

Applications

WB, IHC, ELISA

Recommended dilution

WB 1:500-1:2000; IHC 1:100-1:300; ELISA 1:5000;

Clonality

Polyclonal

Conjugation

Unconjugated

Isotype

IgG

Molecular weight

165 kDa

Formulation

NMDAepsilon2 (phospho Tyr1474) Antibody was tube-contained. Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.

Concentration

1 mg/ml

Purification

NMDAepsilon2 (phospho Tyr1474) Antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Storage

-20 Celsius degree. Avoid repeated freeze/thaw cycles.

Alternative antibody names

Glutamate receptor ionotropic, NMDA 2B antibody, GluN2B antibody, Glutamate receptor subunit epsilon-2 antibody, N-methyl D-aspartate receptor subtype 2B antibody, NMDAR2B antibody, NR2B antibody, N-methyl-D-aspartate receptor subunit 3 antibody, NR3 antibody, hNR3 antibody

Database links

Human UniProt/Swiss-Prot:Q13224;Mouse UniPort/Swiss-Prot: Q01097;Rat UniProt/Swiss-Port: Q00960;Human Entrez Gene: 2904;Mouse Entrez Gene: 14812;Rat Entrez Gene: Rn.9711

Protein names

Glutamate receptor ionotropic, NMDA 2B , GluN2B , Glutamate receptor subunit epsilon-2 , N-methyl D-aspartate receptor subtype 2B , NMDAR2B , NR2B , N-methyl-D-aspartate receptor subunit 3 , NR3 , hNR3

Involvement in disease

Mental retardation, autosomal dominant 6 (MRD6) [MIM:613970]: A disorder characterized by significantly below average general intellectual functioning associated with impairments in adaptive behavior and manifested during the developmental period. . Note: The disease is caused by mutations affecting the gene represented in this entry.; Epileptic encephalopathy, early infantile, 27 (EIEE27) [MIM:616139]: A form of epileptic encephalopathy, a heterogeneous group of severe childhood onset epilepsies characterized by refractory seizures, neurodevelopmental impairment, and poor prognosis. Development is normal prior to seizure onset, after which cognitive and motor delays become apparent. Note: The disease is caused by mutations affecting the gene represented in this entry.; Note: A chromosomal aberrations involving GRIN2B has been found in patients with mental retardation. Translocations t(9;12)(p23;p13.1) and t(10;12)(q21.1;p13.1) with a common breakpoint in 12p13.1.

Research area

All research areas>Channel Proteins>NMDA
(View all antibody categories related to Channel Proteins)

Note

AntibodyPlus can customize NMDAepsilon2 (phospho Tyr1474) Antibody according to your requirement, including bulk product size,etc. Please contact info@antibodyplus.com. AntibodyPlus provide antibody trial sample for your own antibody validation and collects antibody reviews.

Supplier

St John’s Laboratory Ltd.

Product type

Primary antibody

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