SUMF1 蛋白
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- 抗原 See all SUMF1 蛋白
- SUMF1 (Sulfatase Modifying Factor 1 (SUMF1))
- 蛋白类型
- Recombinant
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宿主
- 人
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资源
- HEK-293 Cells
- 应用范围
- Antibody Production (AbP), Standard (STD)
- 产品特性
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- Recombinant human SUMF1 / FGE protein expressed in HEK293 cells.
- Produced with end-sequenced ORF clone
- 纯度
- > 95 % as determined by SDS-PAGE and Coomassie blue staining
- 内毒素水平
- < 0.1 EU per μg protein as determined by LAL test
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- Discover our top product SUMF1 蛋白
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Sulfatase Modifying Factor 1 (SUMF1) (AA 91-374) protein (His tag)
SUMF1 宿主: 人 宿主: 大肠杆菌（E. Coli） Recombinant > 85 % by SDS - PAGE SDS
Sulfatase Modifying Factor 1 (SUMF1) (AA 101-216) protein (His-IF2DI Tag)SUMF1 宿主: 人 宿主: 大肠杆菌（E. Coli） Recombinant Greater than 95 % by SDS-PAGE gel analyses WB, ELISA
Sulfatase Modifying Factor 1 (SUMF1) (AA 89-188) protein (GST tag)SUMF1 宿主: 人 宿主: 小麦胚 Recombinant WB, ELISA, AP, AA
Sulfatase Modifying Factor 1 (SUMF1) protein (Myc-DYKDDDDK Tag)SUMF1 宿主: 人 宿主: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
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- 应用备注
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Recombinant human proteins can be used for:
Native antigens for optimized antibody production
Positive controls in ELISA and other antibody assays - 限制
- 仅限研究用
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- 浓度
- 50 μg/mL
- 缓冲液
- 20 mM Tris-HCl, 150 mM NaCl, 2 mM CaCl2, 10 % Glycerol, pH 7.5. Avoid repeated freeze-thaw cycles. Stable for at least 3 months from receipt of products under proper storage and handling conditions.
- 储存条件
- -80 °C
- 储存方法
- Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.
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- 抗原
- SUMF1 (Sulfatase Modifying Factor 1 (SUMF1))
- 别名
- Sumf1,fge (SUMF1 产品)
- 别名
- AAPA3037 Protein, FGE Protein, AA543204 Protein, AI463102 Protein, AI851573 Protein, sulfatase modifying factor 1 Protein, SUMF1 Protein, Sumf1 Protein
- 背景
- This gene encodes an enzyme that catalyzes the hydrolysis of sulfate esters by oxidizing a cysteine residue in the substrate sulfatase to an active site 3-oxoalanine residue, which is also known as C-alpha-formylglycine. Mutations in this gene cause multiple sulfatase deficiency, a lysosomal storage disorder. Alternative splicing results in multiple transcript variants.
- 分子量
- 38.3 kDa
- NCBI登录号
- NP_877437
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