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Biotin Plus-conjugated ATP1A2-Specific Polyclonal antibody

ATP1A2-Specific Polyclonal Antibody for IHC
Cat No. Biotin-55179

Host / Isotype

Rabbit / IgG

Reactivity

human, mouse

Applications

IHC

ATP1A2, Sodium pump subunit alpha-2, Na(+)/K(+) ATPase alpha-2 subunit, EC:7.2.2.13, ATP1A 2

Formulation:  PBS and Azide
PBS and Azide
Conjugate:  Biotin Plus
Size: 

-/ -


经过测试的应用

Positive IHC detected inmouse heart tissue
Note: suggested antigen retrieval with TE buffer pH 9.0; (*) Alternatively, antigen retrieval may be performed with citrate buffer pH 6.0

推荐稀释比

ApplicationDilution
Immunohistochemistry (IHC)IHC : 1:50-1:500
It is recommended that this reagent should be titrated in each testing system to obtain optimal results.
Sample-dependent, Check data in validation data gallery.

产品信息

Biotin-55179 targets ATP1A2-Specific in IHC applications and shows reactivity with human, mouse samples.

Tested Applications IHC Application Description
Tested Reactivity human, mouse
Immunogen Peptide 种属同源性预测
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Full Name ATPase, Na+/K+ transporting, alpha 2 (+) polypeptide
Synonyms ATP1A2, Sodium pump subunit alpha-2, Na(+)/K(+) ATPase alpha-2 subunit, EC:7.2.2.13, ATP1A 2
Calculated Molecular Weight 112 kDa
Observed Molecular Weight 100 kDa
GenBank Accession NumberNM_000702
Gene Symbol ATP1A2
Gene ID (NCBI) 477
Conjugate Biotin Plus
Form Liquid
Purification MethodAntigen Affinity Purified
UNIPROT IDP50993
Storage Buffer PBS with 50% Glycerol, 0.05% Proclin300, 0.5% BSA, pH 7.3.
Storage ConditionsStore at -20°C. Avoid exposure to light. Stable for one year after shipment. Aliquoting is unnecessary for -20oC storage.

背景介绍

ATP1A2, also named as KIAA0778, belongs to the cation transport ATPase (P-type) family and Type IIC subfamily. It is the catalytic component of the active enzyme, which catalyzes the hydrolysis of ATP coupled with the exchange of sodium and potassium ions across the plasma membrane. Defects in ATP1A2 are the cause of familial hemiplegic migraine type 2 (FHM2). Defects in ATP1A2 are a cause of alternating hemiplegia of childhood (AHC). This antibody is specific to ATP1A2.

实验方案

Product Specific Protocols
IHC protocol for Biotin Plus ATP1A2-Specific antibody Biotin-55179Download protocol
Standard Protocols
Click here to view our Standard Protocols
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