PIMA526491

MAGEA3 Monoclonal Antibody (OTI2B1), Invitrogen™

Manufacturer: Thermo Scientific

Select a Size

Pack Size SKU Availability Price
Each of 1 PIMA526491-Each-of-1 In Stock ₹ 52,198.50

PIMA526491 - Each of 1

₹ 52,198.50

In Stock

Quantity

1

Base Price: ₹ 52,198.50

GST (18%): ₹ 9,395.73

Total Price: ₹ 61,594.23

Antigen

MAGEA3

Classification

Monoclonal

Concentration

1 mg/mL

Formulation

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

Gene Accession No.

P43357

Gene Symbols

MAGEA3

Immunogen

Full length human recombinant protein of MAGEA3 produced in HEK293T cell

Quantity

100μL

Primary or Secondary

Primary

Target Species

Human

Product Type

Antibody

Isotype

IgG2a

Applications

Western Blot

Clone

OTI2B1

Conjugate

Unconjugated

Gene

MAGEA3

Gene Alias

Antigen MZ2-D; cancer/testis antigen 1.3; cancer/testis antigen family 1, member 3; CT1.3; HIP8; HYPD; MAGE family member A3; MAGE3; MAGE-3 antigen; MAGEA3; Mage-a3; MAGEA6; melanoma antigen family A, 3; melanoma antigen family A3; melanoma antigen, family A, 3; melanoma-associated antigen 3; MGC14613

Host Species

Mouse

Purification Method

Affinity Chromatography

Regulatory Status

RUO

Gene ID (Entrez)

4102

Content And Storage

-20° C, Avoid Freeze/Thaw Cycles

Form

Liquid

Related Products

Img

Thermo Scientific

PIPA570209

--

Img

Thermo Scientific

PIPA5118042

--

Img

Thermo Scientific

PIPA584851

--

Img

Thermo Scientific

PIMA191067

--

Img

Novus Biologicals

NB251465

--

Img

Novus Biologicals

NB235062

--

Img

Novus Biologicals

NB234972

--

Img

Novus Biologicals

NB233575

--

Description

  • This gene is a member of the MAGEA gene family
  • The members of this family encode proteins with 50 to 80% sequence identity to each other
  • The promoters and first exons of the MAGEA genes show considerable variability, suggesting that the existence of this gene family enables the same function to be expressed under different transcriptional controls
  • The MAGEA genes are clustered at chromosomal location Xq28
  • They have been implicated in some hereditary disorders, such as dyskeratosis congenita.