FAM36A Protein (Myc-DYKDDDDK Tag)
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- 抗原 See all FAM36A products
- FAM36A (Family with Sequence Similarity 36, Member A (FAM36A))
- 蛋白类型
- Recombinant
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宿主
- 人
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资源
- HEK-293 Cells
- 标记
- This FAM36A 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 FAM36A protein expressed in HEK293 cells.
- Produced with end-sequenced ORF clone
- 纯度
- > 80 % as determined by SDS-PAGE and Coomassie blue staining
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Family with Sequence Similarity 36, Member A (FAM36A) (AA 2-118) protein (rho-1D4 tag)
Crystallography grade FAM36A 宿主: 人 宿主: Insect Cells Recombinant >95 % as determined by SDS PAGE, Size Exclusion Chromatography and Western Blot. SDS, WB, Crys, ELISA
Family with Sequence Similarity 36, Member A (FAM36A) (AA 2-117) protein (rho-1D4 tag)Crystallography grade FAM36A 宿主: 小鼠 宿主: Insect Cells Recombinant >95 % as determined by SDS PAGE, Size Exclusion Chromatography and Western Blot. SDS, WB, Crys, ELISA
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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
- FAM36A (Family with Sequence Similarity 36, Member A (FAM36A))
- 别名
- Fam36a (FAM36A 产品)
- 别名
- FAM36A Protein, 2310005N03Rik Protein, Fam36a Protein, RGD1309105 Protein, cox20 Protein, fam36a Protein, COX20, cytochrome c oxidase assembly factor Protein, COX20 Cox2 chaperone Protein, COX20 cytochrome C oxidase assembly factor Protein, COX20 cytochrome c oxidase assembly factor L homeolog Protein, COX20 Protein, Cox20 Protein, cox20.L Protein
- 背景
- This gene encodes a protein that plays a role in the assembly of cytochrome C oxidase, an important component of the respiratory pathway. It contains two transmembrane helices and localizes to the mitochondrial membrane. Mutations in this gene can cause mitochondrial complex IV deficiency, which results in ataxia and muscle hypotonia. There are multiple pseudogenes for this gene. Alternative splicing results in multiple transcript variants.
- 分子量
- 13.1 kDa
- NCBI登录号
- NP_932342
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