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Home Recombinant Human Proteins MAGEA5 Heavy-labeled protein

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MAGEA5 Mass Spec Standard

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Cat. No. Ref. ID Description Price Availability
PH318575 NM_021049 MAGEA5 MS Standard C13 and N15-labeled recombinant protein (NP_066387), 10 ug $1500 3 weeks
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Also for MAGEA5 (NM_021049)
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OriGene Data
Expression Host:Human HEK293 cells Predicted MW:12.8 kDa
Expression TrueORF clone:RC218575 Protein Sequence: Sequence Link
Tag:C-terminal MYC/DDK * Anti-Myc/DDK antibody Protein family:
Purity:> 80% as determined by SDS-PAGE and Coomassie blue staining
Concentration:> 50 ug/ml as determined by BCA
Labeling Method:Labeled with [U- 13C6, 15N4]-L-Arginine and [U- 13C6, 15N2]-L-Lysine
Buffer and Storage:100 mM glycine, 25 mM Tris-HCl, pH 7.3. Store at -80C. Avoid repeated freeze-thaw cycles. Stable for 3 months from receipt of products under proper storage and handling conditions.
Protein Image
*: DDK-tag is the same as FLAG tag. Flag® is a registered trademark of Sigma-Aldrich

Reference Data
RefSeq: NP_066387 RefSeq Size: 1692 RefSeq ORF: 375
Synonyms : CT1.5; MAGE5; MAGEA4
LocusID: 4104 Cytogenetic: Xq28  
Summary: 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. This MAGEA gene encodes a protein that is C-terminally truncated compared to other family members, and this gene can be alternatively interpreted to be a pseudogene. The protein is represented in this Gene record in accordance with the assumed protein-coding status defined in the literature. Read-through transcription exists between this gene and the upstream melanoma antigen family A, 10 (MAGEA10) gene. [provided by RefSeq, Oct 2011].

 

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