form
liquid
Quality Level
manufacturer/tradename
Novagen®
storage condition
do not freeze
shipped in
wet ice
storage temp.
2-8°C
General description
S蛋白琼脂糖可特异性保留S•标签 融合的蛋白。结合可以以柱的形式或批处理模式进行。使用稍微变性的条件或使用特定的蛋白酶（例如凝血酶或肠激酶）即可对适当的重组蛋白进行洗脱。S-蛋白琼脂糖的载量会发生变化，其数值基于所给定靶蛋白的大小和折叠特性。
它包含 15 个氨基酸的序列 Lys-Glu-Thr-Ala-Ala-Ala-Lys-Phe-Glu-Arg-Gln-His-Met-Asp-Ser （KETAAAKFERQHMDS）。
Application
S 蛋白琼脂糖已用于纯化 S 重组标记融合蛋白。
Legal Information
NOVAGEN is a registered trademark of Merck KGaA, Darmstadt, Germany
Disclaimer
毒性：标准处理（A）
存储类别
12 - Non Combustible Liquids
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
Toshiki Takahashi et al.
EMBO reports, 20(4) (2019-02-26)
Rab family small GTPases are master regulators of distinct steps of intracellular vesicle trafficking in eukaryotic cells. GDP-bound cytoplasmic forms of Rab proteins are prone to aggregation due to the exposure of hydrophobic groups but the machinery that determines the
Xiaoting Liang et al.
Theranostics, 10(17), 7747-7757 (2020-07-21)
Background: Rab22a-NeoF1 fusion gene containing the 1-38aa of Rab22a (Rab22a1-38) plays a decisive role in driving tumor metastasis by activating RhoA via binding to SmgGDS607. However, its intercellular regulation remains unknown. Methods: The Lys7 (K7) acetylation of Rab22a-NeoF1 was initially
Qian Li et al.
Journal of virology, 93(5) (2018-12-14)
Human herpesvirus 8 (HHV-8) viral interleukin-6 (vIL-6) localizes largely to the endoplasmic reticulum (ER) and here associates functionally with both the gp130 signal transducer and the novel ER membrane protein vitamin K epoxide reductase complex subunit 1 variant-2 (VKORC1v2). The
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Starch synthase 2 (SS2) is an important enzyme in leaf starch synthesis, elongating intermediate-length glucan chains. Loss of SS2 results in a distorted starch granule phenotype and altered physiochemical properties, highlighting its importance in starch biosynthesis, however, the post-translational regulation
Gadd45a Protein Promotes Skeletal Muscle Atrophy by Forming a Complex with the Protein Kinase MEKK4.
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Skeletal muscle atrophy is a serious and highly prevalent condition that remains poorly understood at the molecular level. Previous work found that skeletal muscle atrophy involves an increase in skeletal muscle Gadd45a expression, which is necessary and sufficient for skeletal
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| 货号 | GTIN |
|---|---|
| 69704-4 | 07790788052645 |
| 69704-3 | 04055977258967 |
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