NADK2 抗体
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- 抗原 See all NADK2 抗体
- NADK2 (NAD Kinase 2, Mitochondrial (NADK2))
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适用
- 人, 小鼠, 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 NADK2 antibody is un-conjugated
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应用范围
- Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- 交叉反应
- 人, 小鼠, 大鼠
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human C5ORF33
- 亚型
- IgG
- Top Product
- Discover our top product NADK2 Primary Antibody
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anti-NAD Kinase 2, Mitochondrial (NADK2) (AA 16-156) antibody
NADK2 适用: 人 WB, ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-NAD Kinase 2, Mitochondrial (NADK2) antibodyNADK2 适用: 人, 大鼠 WB, ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-NAD Kinase 2, Mitochondrial (NADK2) (AA 122-150) antibodyNADK2 适用: 人, 小鼠 WB, IHC (p) 宿主: 兔 Polyclonal RB27767 unconjugated
anti-NAD Kinase 2, Mitochondrial (NADK2) (AA 215-264) antibodyNADK2 适用: 人, 小鼠, 大鼠, Cow, 犬, 兔, 豚鼠, Pig, Bat, 猴 WB 宿主: 兔 Polyclonal unconjugated
anti-NAD Kinase 2, Mitochondrial (NADK2) (Middle Region) antibodyNADK2 适用: 人, 小鼠, 大鼠, Cow, 犬, 兔, 马, 豚鼠, 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
IHC-P 1:200-400
IF(IHC-P) 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
- NADK2 (NAD Kinase 2, Mitochondrial (NADK2))
- 别名
- C5ORF33 (NADK2 产品)
- 别名
- C5orf33 antibody, MNADK antibody, NADKD1 antibody, ATNADK2 antibody, F8K7.5 antibody, F8K7_5 antibody, NAD KINASE 2 antibody, NAD kinase 2 antibody, NAD kinase 2, mitochondrial antibody, NAD kinase 2 antibody, NADK2 antibody
- 背景
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Synonyms: C5orf33, CE033_HUMAN, Chromosome 5 open reading frame 33, NADKD1.
Background: With 181 million base pairs encoding around 1,000 genes, chromosome 5 is about 6 % of human genomic DNA. It is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is also chromosome 5 associated and is caused by insertions or deletions within the TCOF1 gene. Deletion of the p arm of chromosome 5 leads to Cri du chat syndrome. Deletion of 5q or chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome. The C5orf33 gene product has been provisionally designated C5orf33 pending further characterization.
- 基因ID
- 133686
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