COQ8A 抗体 (AA 501-647)
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- 抗原 See all COQ8A 抗体
- COQ8A (Coenzyme Q8A (COQ8A))
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抗原表位
- AA 501-647
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适用
- 人, 大鼠
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宿主
- 兔
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克隆类型
- 多克隆
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标记
- This COQ8A antibody is un-conjugated
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应用范围
- Western Blotting (WB), ELISA, Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))
- 交叉反应
- 人, 大鼠
- 预测反应
- Mouse,Dog,Cow,Sheep,Pig,Horse,Chicken,Rabbit
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human ADCK3/CABC1
- 亚型
- IgG
- Top Product
- Discover our top product COQ8A Primary Antibody
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anti-Coenzyme Q8A (COQ8A) antibody
COQ8A 适用: 人, 小鼠, 大鼠 WB, IHC 宿主: 兔 Polyclonal unconjugated
anti-Coenzyme Q8A (COQ8A) antibodyCOQ8A 适用: 人, 小鼠, 大鼠 WB, ELISA, IF, ICC 宿主: 兔 Polyclonal unconjugated
anti-Coenzyme Q8A (COQ8A) (AA 1-100) antibodyCOQ8A 适用: 人 WB, ELISA 宿主: 小鼠 Monoclonal 7G1 unconjugated
anti-Coenzyme Q8A (COQ8A) (AA 1-220) antibodyCOQ8A 适用: 人 ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-Coenzyme Q8A (COQ8A) (Internal Region) antibodyCOQ8A 适用: 人, 小鼠, 大鼠 WB, ELISA, IF, IHC 宿主: 兔 Polyclonal unconjugated
anti-Coenzyme Q8A (COQ8A) (Center) antibodyCOQ8A 适用: 人, 小鼠, 大鼠, Cow WB, IF, IHC, IC 宿主: 兔 Polyclonal unconjugated
anti-Coenzyme Q8A (COQ8A) (AA 146-195) antibodyCOQ8A 适用: 人, 小鼠, 大鼠, Cow, 犬, 豚鼠, 马, 兔, Hamster, 猴 WB 宿主: 兔 Polyclonal unconjugated
anti-Coenzyme Q8A (COQ8A) (AA 1-647) antibodyCOQ8A 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
anti-Coenzyme Q8A (COQ8A) antibodyCOQ8A 适用: 人 WB, IF 宿主: 小鼠 Monoclonal 216CT7-5-1 unconjugated
anti-Coenzyme Q8A (COQ8A) (N-Term) antibodyCOQ8A 适用: 人, 小鼠, 大鼠, Cow, 犬, 豚鼠, 马, 兔, 斑马鱼 WB 宿主: 兔 Polyclonal unconjugated
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- 应用备注
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WB 1:300-5000
ELISA 1:500-1000
IHC-P 1:200-400
IHC-F 1:100-500
IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200 - 限制
- 仅限研究用
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- 状态
- Liquid
- 浓度
- 1 μg/μL
- 缓冲液
- 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.
- 储存液
- ProClin
- 注意事项
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
- 储存条件
- 4 °C,-20 °C
- 储存方法
- Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
- 有效期
- 12 months
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- 抗原
- COQ8A (Coenzyme Q8A (COQ8A))
- 别名
- CABC1 (COQ8A 产品)
- 别名
- ARCA2 antibody, CABC1 antibody, COQ10D4 antibody, COQ8 antibody, SCAR9 antibody, 4632432J16Rik antibody, AI462003 antibody, Cabc1 antibody, mKIAA0451 antibody, cabc1 antibody, Adck3 antibody, adck4 antibody, si:dkey-114g7.2 antibody, coenzyme Q8A antibody, aarF domain containing kinase 3 antibody, coenzyme Q8B antibody, COQ8A antibody, Coq8a antibody, coq8a antibody, ADCK3 antibody, coq8b antibody
- 背景
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Synonyms: mitochondrial, aarF domain containing protein kinase 3, aarF domain-containing protein kinase 3, ADCK 3, ADCK3, ADCK3_HUMAN, CABC 1, Chaperone ABC1 activity of bc1 complex S.pombe like, Chaperone ABC1 activity of bc1 complex homolog, Chaperone ABC1 like, Chaperone activity of bc1 complex like, Chaperone activity of bc1 complex like mitochondrial, Chaperone activity of bc1 complex-like, Chaperone-ABC1-like, Coenzyme Q8 homolog, COQ 8, COQ8.
Background: May be a chaperone-like protein essential for the proper conformation and functioning of protein complexes in the respiratory chain.Tissue specificity:Ubiquitously expressed with a relatively greater abundance in heart and skeletal muscle.Involvement in disease:Defects in ADCK3 are a cause of coenzyme Q10 deficiency (CoQ10 deficiency). CoQ10 deficiency is an autosomal recessive disorder with variable manifestations. It can be associated with three main clinical phenotypes: a predominantly myopathic form with central nervous system involvement, an infantile encephalomyopathy with renal dysfunction and an ataxic form with cerebellar atrophy.Defects in ADCK3 are the cause of spinocerebellar ataxia autosomal recessive type 9 (SCAR9) [MIM:612016], also known as autosomal recessive cerebellar ataxia type 2 (ARCA2). Spinocerebellar ataxia is a clinically and genetically heterogeneous group of cerebellar disorders. Patients show progressive incoordination of gait and often poor coordination of hands, speech and eye movements, due to degeneration of the cerebellum with variable involvement of the brainstem and spinal cord. SCAR9 is an autosomal recessive form characterized by gait ataxia and cerebellar atrophy with slow progression and few associated features. Patients can manifest brisk tendon reflexes and Hoffmann sign, mild psychomotor retardation, mild axonal degeneration of the sural nerve, exercise intolerance and elevated serum lactate.
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