PIMA527223

PRRT2 Monoclonal Antibody (OTI9H8), Invitrogen™

Manufacturer: Thermo Scientific

Select a Size

Pack Size SKU Availability Price
Each of 1 PIMA527223-Each-of-1 In Stock ₹ 52,287.50

PIMA527223 - Each of 1

₹ 52,287.50

In Stock

Quantity

1

Base Price: ₹ 52,287.50

GST (18%): ₹ 9,411.75

Total Price: ₹ 61,699.25

Antigen

PRRT2

Classification

Monoclonal

Concentration

1 mg/mL

Formulation

PBS with 1% BSA, 50% glycerol and 0.02% sodium azide; pH 7.3

Gene Accession No.

E9PUL5, Q7Z6L0

Gene Symbols

PRRT2

Immunogen

Human recombinant protein fragment corresponding to amino acids 152-268 of PRRT2 produced in E.coli

Quantity

100μL

Primary or Secondary

Primary

Target Species

Human, Mouse

Product Type

Antibody

Isotype

IgG1

Applications

Immunohistochemistry (Paraffin), Western Blot

Clone

OTI9H8

Conjugate

Unconjugated

Gene

PRRT2

Gene Alias

1500031I19Rik; AI195361; BFIC2; BFIS2; Dispanin subfamily B member 3; DSPB3; dystonia 10; DYT10; EKD1; FICCA; ICCA; IFITMD1; infantile convulsions and paroxysmal choreoathetosis; interferon induced transmembrane protein domain containing 1; PKC; proline rich transmembrane protein 2; proline-rich transmembrane protein 2; PRRT2; RGD1564195

Host Species

Mouse

Purification Method

Affinity Chromatography

Regulatory Status

RUO

Gene ID (Entrez)

112476, 69017

Content And Storage

-20° C, Avoid Freeze/Thaw Cycles

Form

Liquid

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Description

  • The proline-rich transmembrane protein 2 (PRRT2) contains a proline-rich domain in its N-terminal half and is predominantly expressed in brain and spinal cord in embryonic and postnatal stages
  • While little is known of the function of this protein, mutations in PRRT2 have been shown to be the causative gene of paroxysmal kinesigenic dyskinesia, which is characterized by recurrent, brief attacks of abnormal involuntary movements induced by sudden voluntary movements
  • Recent studies have shown that PRRT2 may also be involved in some forms of benign familial infantile epilepsy (BFIE), an autosomal dominant epilepsy syndrome.