PIPA5103303

MAGEA9 Polyclonal Antibody, Invitrogen™

Manufacturer: Thermo Scientific

Select a Size

Pack Size SKU Availability Price
Each of 1 PIPA5103303-Each-of-1 In Stock ₹ 41,607.50

PIPA5103303 - Each of 1

₹ 41,607.50

In Stock

Quantity

1

Base Price: ₹ 41,607.50

GST (18%): ₹ 7,489.35

Total Price: ₹ 49,096.85

Antigen

MAGEA9

Classification

Polyclonal

Conjugate

Unconjugated

Gene

MAGEA9

Gene Alias

Cancer/testis antigen 1.9; cancer/testis antigen family 1, member 9; CT1.9; MAGE family member A9; MAGE9; MAGE-9 antigen; MAGEA9; MAGEA9A; MAGEA9B; melanoma antigen family A, 9; melanoma antigen family A9; melanoma-associated antigen 9; MGC114427; similar to melanoma antigen family A, 5; uncharacterized protein LOC317297

Host Species

Rabbit

Purification Method

Affinity chromatography

Regulatory Status

RUO

Gene ID (Entrez)

4108

Content And Storage

-20°C

Form

Liquid

Applications

Western Blot

Concentration

1 mg/mL

Formulation

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

Gene Accession No.

P43362

Gene Symbols

MAGEA9

Immunogen

A synthesized peptide derived from human MAGEA9, MAGEA9B(Accession P43362), corresponding to amino acid residues M1-S41.

Quantity

100 μL

Primary or Secondary

Primary

Target Species

Human

Product Type

Antibody

Isotype

IgG

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Description

  • Antibody detects endogenous levels of total MAGEA9
  • MAGEA9 is a member of the MAGEA gene family
  • The members of this family have their entire coding sequences located in the last exon, and the encoded proteins show 50 to 80% sequence identity between 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 expressed at a high level in a number of tumors of various histologic types, and are silent in normal tissues with the exception of testis and placenta
  • The MAGEA genes are clustered on chromosome Xq28
  • They may be implicated in some hereditary disorders, such as dyskeratosis congenita.