MAGEA6 antibody (Middle Region)
Quick Overview for MAGEA6 antibody (Middle Region) (ABIN2782499)
Target
See all MAGEA6 AntibodiesReactivity
Host
Clonality
Conjugate
Application
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Binding Specificity
- Middle Region
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Sequence
- APEEKIWEEL SVLEVFEGRE DSIFGDPKKL LTQYFVQENY LEYRQVPGSD
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Predicted Reactivity
- Dog: 83%, Horse: 83%, Human: 100%, Mouse: 83%, Pig: 83%, Rabbit: 83%, Rat: 83%
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Characteristics
- This is a rabbit polyclonal antibody against MAGEA6. 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 MAGEA6
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Application Notes
- Optimal working dilutions should be determined experimentally by the investigator.
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Comment
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Antigen size: 314 AA
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Restrictions
- For Research Use only
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Format
- Liquid
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Concentration
- Lot specific
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Buffer
- Liquid. 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
- Avoid repeated freeze-thaw cycles.
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Storage
- -20 °C
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Storage Comment
- For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
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- MAGEA6 (Melanoma Antigen Family A, 6 (MAGEA6))
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Alternative Name
- MAGEA6
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Background
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MAGEA6 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.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. Two transcript variants encoding the same protein have been identified for this gene.
Alias Symbols: MAGE-3b, MAGE3B, MAGE6, MGC52297, CT1.6
Protein Interaction Partner: KLHL38, MORN3, LCORL, IQUB, MIPOL1, ANKRD26P1, SNAP47, HAUS1, ATPAF2, ELMOD3, RASSF4, SH2D4A, LSM2, CCDC146, STAMBPL1, S100A14, FAM214A, LIN37, RCOR3, GFOD1, FRMPD1, ACOT7, EXOC5, BET1, TXNDC9, AKAP9, ATP6V1G1, BCL7B, SNX4, NCK2, TULP3, STX5, RPL37A, PDE4
Protein Size: 314 -
Molecular Weight
- 35 kDa
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Gene ID
- 4105
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NCBI Accession
- NM_005363, NP_005354
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UniProt
- P43360
Target
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