MAGEA9 antibody (Middle Region)
Quick Overview for MAGEA9 antibody (Middle Region) (ABIN2776439)
Target
See all MAGEA9 AntibodiesReactivity
Host
Clonality
Conjugate
Application
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Binding Specificity
- Middle Region
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Purpose
- MAGEA9 Antibody - middle region
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Sequence
- ALKLKVAELV HFLLHKYRVK EPVTKAEMLE SVIKNYKRYF PVIFGKASEF
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Predicted Reactivity
- Cow: 77%, Dog: 79%, Horse: 79%, Human: 100%, Pig: 79%, Rabbit: 85%, Rat: 85%, Yeast: 77%
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Characteristics
- This is a rabbit polyclonal antibody against MAGEA9. It was validated on Western Blot using a cell lysate as a positive control.
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Purification
- Affinity Purified
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Immunogen
- The immunogen is a synthetic peptide directed towards the middle region of human MAGEA9
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Application Notes
- Optimal working dilution should be determined by the investigator.
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Comment
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We also sell a specific blocking peptide that can be used in combination with this antibody. You can find the blocking peptide under AAP35768-100UG
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Restrictions
- For Research Use only
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Format
- Liquid
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Concentration
- 0.5 mg/mL
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Buffer
- Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.
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Preservative
- Sodium azide
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Precaution of Use
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Handling Advice
- prevent freeze-thaw cycles
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Storage
- 4 °C,-20 °C
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Storage Comment
- For short term use, store at 2-8C up to 1 week. For long term storage, store at -20 °C in small aliquots to prevent freeze-thaw cycles.
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- MAGEA9 (Melanoma Antigen Family A, 9 (MAGEA9))
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Alternative Name
- MAGEA9
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Background
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Background Information: MAGEA9 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. This pseudogene is a member of the cytochrome P450 gene superfamily. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. It is possible that, in rare cases, a combination of two SNPs in this gene may result in an open reading frame encoding a functional enzyme which metabolizes codeine to morphine. This locus is part of a cluster of cytochrome P450 genes on chromosome 22q13.1. 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.
Gene Name: Melanoma antigen family A, 9
Alternative Symbols: CT1.9, MAGE9
Protein Name: Melanoma-associated antigen 9
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Molecular Weight
- 35kDa
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Gene ID
- 4108
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NCBI Accession
- NP_005356
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UniProt
- P43362
Target
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