CLN6 Protein (Myc-DYKDDDDK Tag)
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- 抗原 See all CLN6 蛋白
- CLN6 (Ceroid-Lipofuscinosis, Neuronal 6, Late Infantile, Variant (CLN6))
- 蛋白类型
- Recombinant
- 宿主
- 人
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资源
- HEK-293 Cells
- 标记
- This CLN6 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 CLN6 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 CLN6 蛋白
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Ceroid-Lipofuscinosis, Neuronal 6, Late Infantile, Variant (CLN6) (AA 1-311) protein (GST tag)
CLN6 宿主: 人 宿主: 小麦胚 Recombinant ELISA, WB, AA, AP
Ceroid-Lipofuscinosis, Neuronal 6, Late Infantile, Variant (CLN6) (AA 1-311) protein (Strep Tag)Crystallography grade CLN6 宿主: 人 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
- CLN6 (Ceroid-Lipofuscinosis, Neuronal 6, Late Infantile, Variant (CLN6))
- 别名
- Cln6 (CLN6 产品)
- 别名
- 1810065L06Rik Protein, AW743417 Protein, D9Bwg1455e Protein, nclf Protein, CLN4A Protein, HsT18960 Protein, cln6 Protein, zgc:103565 Protein, ceroid-lipofuscinosis, neuronal 6 Protein, CLN6, transmembrane ER protein Protein, CLN6, transmembrane ER protein S homeolog Protein, ceroid-lipofuscinosis, neuronal 6, late infantile, variant Protein, CLN6, transmembrane ER protein a Protein, Cln6 Protein, CLN6 Protein, cln6.S Protein, cln6a Protein
- 背景
- This gene is one of eight which have been associated with neuronal ceroid lipofuscinoses (NCL). Also referred to as Batten disease, NCL comprises a class of autosomal recessive, neurodegenerative disorders affecting children. The genes responsible likely encode proteins involved in the degradation of post-translationally modified proteins in lysosomes. The primary defect in NCL disorders is thought to be associated with lysosomal storage function.
- 分子量
- 35.7 kDa
- NCBI登录号
- NP_060352
- 途径
- Glycosaminoglycan Metabolic Process
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