Recombinant Human PSAP protein (His Tag)

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- 表达系统: E.coli
- 蛋白编码: P07602
别称 |
GLBA;PSAP;SAP1p;proactivator polypeptide;prosaposin
|
表达系统 |
E.coli
|
序列 |
Gly17-Asn524
|
蛋白编码 |
P07602
|
种属 |
Human
|
计算分子量 |
55.8 kDa
|
表观分子量 |
45 kDa
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标签 |
N-His
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生物活性 |
Not validated for activity
|
纯度 |
> 95% as determined by reducing SDS-PAGE.
|
内毒素 |
< 10 EU/mg of the protein as determined by the LAL method
|
保存条件 |
Generally, lyophilized proteins are stable for up to 12 months when stored at -20 to -80℃. Reconstituted protein solution can be stored at 4-8℃ for 2-7 days. Aliquots of reconstituted samples are stable at < -20℃ for 3 months.
|
运输条件 |
This product is provided as lyophilized powder which is shipped with ice packs.
|
制剂 |
Lyophilized from a 0.2 μm filtered solution in PBS with 5% Trehalose and 5% Mannitol.
|
复溶方法 |
It is recommended that sterile water be added to the vial to prepare a stock solution of 0.5 mg/mL. Concentration is measured by UV-Vis.
|
背景 |
This gene encodes a highly conserved preproprotein that is proteolytically processed to generate four main cleavage products including saposins A, B, C, and D. Each domain of the precursor protein is approximately 80 amino acid residues long with nearly identical placement of cysteine residues and glycosylation sites. Saposins A-D localize primarily to the lysosomal compartment where they facilitate the catabolism of glycosphingolipids with short oligosaccharide groups. The precursor protein exists both as a secretory protein and as an integral membrane protein and has neurotrophic activities. Mutations in this gene have been associated with Gaucher disease and metachromatic leukodystrophy. Alternative splicing results in multiple transcript variants, at least one of which encodes an isoform that is proteolytically processed.
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实验操作视频
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