MAGEA8 Antibody | 29-721

MAGEA8 Antibody | 29-721 | Gentaur UK, US & Europe Distribution

Host: Rabbit

Reactivity: Human

Homology: N/A

Immunogen: Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human MAGEA8.

Research Area: Cancer

Tested Application: E, WB, IHC

Application: MAGEA8 antibody can be used for detection of MAGEA8 by ELISA at 1:62500. MAGEA8 antibody can be used for detection of MAGEA8 by western blot at 0.5 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50, 000 - 100, 000.

Specificiy: N/A

Positive Control 1: Cat. No. 1309 - Human Placenta Lysate

Positive Control 2: N/A

Positive Control 3: N/A

Positive Control 4: N/A

Positive Control 5: N/A

Positive Control 6: N/A

Molecular Weight: 35 kDa

Validation: N/A

Isoform: N/A

Purification: Antibody is purified by peptide affinity chromatography method.

Clonality: Polyclonal

Clone: N/A

Isotype: N/A

Conjugate: Unconjugated

Physical State: Liquid

Buffer: Purified antibody supplied in 1x PBS buffer with 0.09% (w/v) sodium azide and 2% sucrose.

Concentration: batch dependent

Storage Condition: For short periods of storage (days) store at 4˚C. For longer periods of storage, store MAGEA8 antibody at -20˚C. As with any antibody avoid repeat freeze-thaw cycles.

Alternate Name: MAGEA8, MAGE8, MGC2182, CT1.8

User Note: Optimal dilutions for each application to be determined by the researcher.

BACKGROUND: MAGEA8 is a member of the MAGEA family. The members of this family with 50 to 80% sequence identity to each other. They have been implicated in some hereditary disorders, such as dyskeratosis congenita.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.