FEMA549936

MFN2 Recombinant Rabbit Monoclonal Antibody (10F6), Invitrogen™

Manufacturer: Thermo Scientific

Select a Size

Pack Size SKU Availability Price
Each of 1 FEMA549936-Each-of-1 In Stock ₹ 37,202.00

FEMA549936 - Each of 1

₹ 37,202.00

In Stock

Quantity

1

Base Price: ₹ 37,202.00

GST (18%): ₹ 6,696.36

Total Price: ₹ 43,898.36

Antigen

MFN2

Classification

Recombinant Monoclonal

Concentration

1.5 mg/mL

Formulation

PBS with 50% glycerol and 0.02% sodium azide, pH 7.4

Gene Accession No.

O95140

Gene Symbols

MFN2

Immunogen

A synthesized peptide derived from human Mitofusin 2

Quantity

100 μL

Primary or Secondary

Primary

Target Species

Human

Form

Liquid

Applications

ELISA, Immunohistochemistry (Paraffin)

Clone

10F6

Conjugate

Unconjugated

Gene

MFN2

Gene Alias

CMT2A, CMT2A2, CPRP 1, CPRP1, D630023P19Rik, Fzo, HMSN6A, HSG, HSG protein, hyperplasia suppressor, hypertension related protein 1, hypertension-related protein, hypertension-related protein 1, Kiaa0214, LOW QUALITY PROTEIN: mitofusin-2, Marf, MFN 2, MFN2, mg:cb01g09, Mitochondrial assembly regulatory factor, mitochondrial transmembrane GTPase FZO1A, mitofusin 2, Mitofusin2, mitofusin-2, si:dkeyp-104h9.2, Transmembrane GTPase MFN2, wu:fb79a11

Host Species

Rabbit

Purification Method

Affinity chromatography

Regulatory Status

RUO

Gene ID (Entrez)

9927

Content And Storage

-20°C or -80°C if preferred

Isotype

IgG

Related Products

Img

Thermo Scientific

FEMA550155

--

Img

Thermo Scientific

FEMA549939

--

Img

Thermo Scientific

FEMA549793

--

Img

Thermo Scientific

FEMA550167

--

Img

Thermo Scientific

FEMA550149

--

Img

Thermo Scientific

FEMA549884

--

Img

Thermo Scientific

FEMA550033

--

Img

Thermo Scientific

FEMA550055

--

Description

  • This gene encodes a mitochondrial membrane protein that participates in mitochondrial fusion and contributes to the maintenance and operation of the mitochondrial network
  • This protein is involved in the regulation of vascular smooth muscle cell proliferation, and it may play a role in the pathophysiology of obesity
  • Mutations in this gene cause Charcot-Marie-Tooth disease type 2A2, and hereditary motor and sensory neuropathy VI, which are both disorders of the peripheral nervous system
  • Defects in this gene have also been associated with early-onset stroke
  • Two transcript variants encoding the same protein have been identified.