DDHD1 Protein (Myc-DYKDDDDK Tag)
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- 抗原 See all DDHD1 蛋白
- DDHD1 (DDHD Domain Containing 1 (DDHD1))
- 蛋白类型
- Recombinant
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宿主
- 人
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资源
- HEK-293 Cells
- 标记
- This DDHD1 protein is labelled with Myc-DYKDDDDK Tag.
- 应用范围
- Antibody Production (AbP), Standard (STD)
- 产品特性
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- Recombinant human DDHD1 protein expressed in HEK293 cells.
- Produced with end-sequenced ORF clone
- 纯度
- > 80 % as determined by SDS-PAGE and Coomassie blue staining
- Top Product
- Discover our top product DDHD1 蛋白
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DDHD Domain Containing 1 (DDHD1) (AA 1-872) protein (GST tag)
DDHD1 宿主: 人 宿主: 小麦胚 Recombinant ELISA, WB, AA, AP
DDHD Domain Containing 1 (DDHD1) (AA 1-900) protein (Strep Tag)Crystallography grade DDHD1 宿主: 人 宿主: Tobacco (Nicotiana tabacum) Recombinant >80 % as determined by SDS PAGE, Size Exclusion Chromatography and Western Blot. ELISA, WB, SDS
DDHD Domain Containing 1 (DDHD1) (AA 1-547) protein (Strep Tag)Crystallography grade DDHD1 宿主: 小鼠 宿主: Tobacco (Nicotiana tabacum) Recombinant ≥ 80 % as determined by SDS PAGE, Size Exclusion Chromatography and Western Blot. ELISA, WB, SDS
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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 - 说明
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The tag is located at the C-terminal.
- 限制
- 仅限研究用
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- 浓度
- 50 μg/mL
- 缓冲液
- 25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
- 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
- DDHD1 (DDHD Domain Containing 1 (DDHD1))
- 别名
- Ddhd1 (DDHD1 产品)
- 别名
- ddhd1 Protein, si:dkey-29m11.6 Protein, si:dkey-63j12.5 Protein, PA-PLA1 Protein, PAPLA1 Protein, SPG28 Protein, 4921528E07Rik Protein, 9630061G18Rik Protein, C85251 Protein, mKIAA1705 Protein, DDHD domain containing 1 Protein, DDHD domain containing 1b Protein, CBR-IPLA-1 protein Protein, DDHD domain containing 1 L homeolog Protein, Ddhd1 Protein, DDHD1 Protein, ddhd1b Protein, LOAG_17210 Protein, ddhd1.L Protein
- 背景
- This gene is a member of the intracellular phospholipase A1 gene family. The protein encoded by this gene preferentially hydrolyzes phosphatidic acid. It is a cytosolic protein with some mitochondrial localization, and is thought to be involved in the regulation of mitochondrial dynamics. Overexpression of this gene causes fragmentation of the tubular structures in mitochondria, while depletion of the gene results in mitochondrial tubule elongation. Deletion of this gene in male mice caused fertility defects, resulting from disruption in the organization of the mitochondria during spermiogenesis. In humans, mutations in this gene have been associated with hereditary spastic paraplegia (HSP), also known as Strumpell-Lorrain disease, or, familial spastic paraparesis (FSP). This inherited disorder is characterized by progressive weakness and spasticity of the legs. Alternative splicing results in multiple transcript variants encoding different isoforms.
- 分子量
- 96.9 kDa
- NCBI登录号
- NP_085140
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