
Thermo Fisher Scientific Human PHKG2, GST Tag Recombinant Protein
인간 PHKG2 단백질을 곤충 세포에서 발현한 GST 태그 재조합 단백질입니다. 키나아제 분석에 적합하며, 고순도 정제된 액상 형태입니다. -80°C에서 보관하며, 연구용으로만 사용 가능합니다.
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Thermo Fisher Scientific Human PHKG2, GST Tag Recombinant Protein
Applications
- Kinase Assay (KA)
Tested Dilution
- Assay-dependent
Product Specifications
| 항목 | 내용 |
|---|---|
| Species | Human |
| Expression System | Insect cells |
| Amino Acid Sequence | Full length |
| Tag | GST-tag |
| Molecular Weight | 73.9 kDa |
| Class | Recombinant |
| Type | Protein |
| Conjugate | Unconjugated |
| Form | Liquid |
| Concentration | See Label |
| Purification | Purified |
| Storage Buffer | 50 mM Tris, pH 7.5, with 2 mM DTT, 0.02% Triton X-100, 50% glycerol, 150 mM NaCl, 0.5 mM EDTA |
| Contains | No preservative |
| Storage Conditions | -80°C, Avoid Freeze/Thaw Cycles |
| Shipping Conditions | Dry ice |
Product Specific Information
For maximum recovery, please spin prior to use.
Unless noted below, aliquots of the 5 µg, 10 µg, and 20 µg sizes of kinase are not recommended, as materials can be used in original packaging until exhausted.
For larger sizes, the number of freeze/thaws may be reduced by preparing aliquots; aliquots below 20 µL are not recommended.
Please never store a kinase diluted.
If properly stored at -80°C, this product is guaranteed for 6 months from date of purchase.
Protein Form: Full Length
Target Information
PHKG2 is a testis/liver isoform of the phosphorylase kinase gamma subunit.
Phosphorylase kinase is a polymer of 16 subunits — four each of alpha, beta, gamma, and delta.
- Alpha subunit: skeletal muscle and hepatic isoforms (two different genes)
- Beta subunit: same in both isoforms (one gene)
- Gamma subunit: includes skeletal muscle and hepatic isoforms; hepatic isoform encoded by PHKG2
- Delta subunit: calmodulin, encoded by three different genes
The gamma subunits contain the active site of the enzyme, whereas the alpha and beta subunits have regulatory functions controlled by phosphorylation.
The delta subunit mediates calcium dependence of the enzyme.
Mutations in PHKG2 cause glycogen storage disease type 9C (autosomal liver glycogenosis).
Alternatively spliced transcript variants encoding different isoforms have been identified in PHKG2.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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