TUFM 抗体 (Middle Region)
Quick Overview for TUFM 抗体 (Middle Region) (ABIN2787734)
抗原
See all TUFM (Tufm) 抗体适用
宿主
克隆类型
标记
应用范围
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抗原表位
- Middle Region
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序列
- PEKELAMPGE DLKFNLILRQ PMILEKGQRF TLRDGNRTIG TGLVTNTLAM
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预测反应
- Cow: 93%, Dog: 100%, Guinea Pig: 93%, Horse: 93%, Human: 100%, Mouse: 86%, Rabbit: 93%, Rat: 93%, Yeast: 77%, Zebrafish: 86%
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产品特性
- This is a rabbit polyclonal antibody against TUFM. It was validated on Western Blot using a cell lysate as a positive control.
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纯化方法
- Affinity Purified
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免疫原
- The immunogen is a synthetic peptide directed towards the middle region of human TUFM
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应用备注
- Optimal working dilutions should be determined experimentally by the investigator.
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说明
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Antigen size: 455 AA
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限制
- 仅限研究用
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状态
- Liquid
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浓度
- Lot specific
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缓冲液
- Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.
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储存液
- Sodium azide
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注意事项
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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注意事项
- Avoid repeated freeze-thaw cycles.
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储存条件
- -20 °C
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储存方法
- For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
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: "hCOA3 stabilizes cytochrome c oxidase 1 (COX1) and promotes cytochrome c oxidase assembly in human mitochondria." in: The Journal of biological chemistry, Vol. 288, Issue 12, pp. 8321-31, (2013) (PubMed).
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: "hCOA3 stabilizes cytochrome c oxidase 1 (COX1) and promotes cytochrome c oxidase assembly in human mitochondria." in: The Journal of biological chemistry, Vol. 288, Issue 12, pp. 8321-31, (2013) (PubMed).
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- TUFM (Tufm) (Tu Translation Elongation Factor, Mitochondrial (Tufm))
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别名
- TUFM
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背景
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TUFM is a protein which participates in protein translation in mitochondria. Mutations in this gene have been associated with combined oxidative phosphorylation deficiency resulting in lactic acidosis and fatal encephalopathy. This gene encodes a protein which participates in protein translation in mitochondria. Mutations in this gene have been associated with combined oxidative phosphorylation deficiency resulting in lactic acidosis and fatal encephalopathy. A pseudogene has been identified on chromosome 17. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.
Alias Symbols: COXPD4, EF-TuMT, EFTU, P43
Protein Interaction Partner: FAM9B, FUNDC1, CMTM5, ARL6IP1, HUWE1, FUS, SUMO2, SUMO3, SPRTN, UBC, MDM2, ASB12, ASB14, ASB10, ASB17, SUZ12, BMI1, RNF2, TUBB2A, XPO1, TUBB6, CAMK1D, NSFL1C, IPO9, UBXN1, DCPS, PROSC, PDIA4, PLAA, GTF3C4, NAE1, PPP5C, PPP1R2, PAFAH1B2, HK1, HEXB, GAPDH,
Protein Size: 455 -
分子量
- 50 kDa
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基因ID
- 7284
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NCBI登录号
- NM_003321, NP_003312
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UniProt
- P49411
抗原
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