PYGM (NM_005609) Human Mass Spec Standard
CAT#: PH312365
PYGM MS Standard C13 and N15-labeled recombinant protein (NP_005600)
View other "PYGM" proteins (6)
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CNY 19520.00
CNY 4840.00
Specifications
| Product Data | |
| Description | PYGM MS Standard C13 and N15-labeled recombinant protein (NP_005600) |
| Species | Human |
| Expression Host | HEK293 |
| Expression cDNA Clone or AA Sequence | RC212365 |
| Predicted MW | 96.9 kDa |
| Protein Sequence |
>RC212365 representing NM_005609
Red=Cloning site Green=Tags(s) MSRPLSDQEKRKQISVRGLAGVENVTELKKNFNRHLHFTLVKDRNVATPRDYYFALAHTVRDHLVGRWIR TQQHYYEKDPKRIYYLSLEFYMGRTLQNTMVNLALENACDEATYQLGLDMEELEEIEEDAGLGNGGLGRL AACFLDSMATLGLAAYGYGIRYEFGIFNQKISGGWQMEEADDWLRYGNPWEKARPEFTLPVHFYGHVEHT SQGAKWVDTQVVLAMPYDTPVPGYRNNVVNTMRLWSAKAPNDFNLKDFNVGGYIQAVLDRNLAENISRVL YPNDNFFEGKELRLKQEYFVVAATLQDIIRRFKSSKFGCRDPVRTNFDAFPDKVAIQLNDTHPSLAIPEL MRILVDLERMDWDKAWDVTVRTCAYTNHTVLPEALERWPVHLLETLLPRHLQIIYEINQRFLNRVAAAFP GDVDRLRRMSLVEEGAVKRINMAHLCIAGSHAVNGVARIHSEILKKTIFKDFYELEPHKFQNKTNGITPR RWLVLCNPGLAEVIAERIGEDFISDLDQLRKLLSFVDDEAFIRDVAKVKQENKLKFAAYLEREYKVHINP NSLFDIQVKRIHEYKRQLLNCLHVITLYNRIKREPNKFFVPRTVMIGGKAAPGYHMAKMIIRLVTAIGDV VNHDPAVGDRLRVIFLENYRVSLAEKVIPAADLSEQISTAGTEASGTGNMKFMLNGALTIGTMDGANVEM AEEAGEENFFIFGMRVEDVDKLDQRGYNAQEYYDRIPELRQVIEQLSSGFFSPKQPDLFKDIVNMLMHHD RFKVFADYEDYIKCQEKVSALYKNPREWTRMVIRNIATSGKFSSDRTIAQYAREIWGVEPSRQRLPAPDE AI TRTRPLEQKLISEEDLAANDILDYKDDDDKV |
| Tag | C-Myc/DDK |
| Purity | > 80% as determined by SDS-PAGE and Coomassie blue staining |
| Concentration | >0.05 µg/µL as determined by microplate BCA method |
| Labeling Method | Labeled with [U- 13C6, 15N4]-L-Arginine and [U- 13C6, 15N2]-L-Lysine |
| Buffer | 25 mM Tris-HCl, 100 mM glycine, pH 7.3 |
| Reference Data | |
| RefSeq | NP_005600 |
| RefSeq Size | 3447 |
| RefSeq ORF | 2526 |
| Synonyms | GSD5 |
| Locus ID | 5837 |
| Cytogenetics | 11q13.1 |
| Summary | This gene encodes a muscle enzyme involved in glycogenolysis. Highly similar enzymes encoded by different genes are found in liver and brain. Mutations in this gene are associated with McArdle disease (myophosphorylase deficiency), a glycogen storage disease of muscle. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Sep 2009] |
| Protein Families | Druggable Genome |
| Protein Pathways | Insulin signaling pathway, Starch and sucrose metabolism |
Documents
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Resources
| 蛋白相关资源 |
Other Versions
| SKU | Description | Size | Price |
|---|---|---|---|
| LC401719 | PYGM HEK293T cell transient overexpression lysate (as WB positive control) |
CNY 1470.00 |
|
| LC431600 | PYGM HEK293T cell transient overexpression lysate (as WB positive control) |
CNY 1470.00 |
|
| LY401719 | Transient overexpression lysate of phosphorylase, glycogen, muscle (PYGM), transcript variant 1 |
CNY 4840.00 |
|
| LY431600 | Transient overexpression lysate of phosphorylase, glycogen, muscle (PYGM), transcript variant 2 |
CNY 4840.00 |
|
| TP312365 | Recombinant protein of human phosphorylase, glycogen, muscle (PYGM), 20 µg |
CNY 2900.00 |
|
| TP328572 | Recombinant protein of human phosphorylase, glycogen, muscle (PYGM), transcript variant 2, 20 µg |
CNY 2900.00 |
