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- 抗原 See all FASTKD1 products
- FASTKD1 (FAST Kinase Domains 1 (FASTKD1))
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适用
- 人
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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 FASTKD1 antibody is un-conjugated
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应用范围
- ELISA, Immunohistochemistry (IHC)
- 产品特性
- Polyclonal Antibody
- 纯化方法
- Affinity purification
- 免疫原
- Recombinant protein of human FASTKD1
- 亚型
- IgG
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anti-FAST Kinase Domains 1 (FASTKD1) (AA 638-847) antibody
FASTKD1 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
anti-FAST Kinase Domains 1 (FASTKD1) (AA 2-99) antibodyFASTKD1 适用: 人 ELISA, WB 宿主: 小鼠 Polyclonal unconjugated
anti-FAST Kinase Domains 1 (FASTKD1) antibodyFASTKD1 适用: 人, 小鼠, 大鼠 IHC 宿主: 兔 Polyclonal unconjugated
anti-FAST Kinase Domains 1 (FASTKD1) (Internal Region) antibodyFASTKD1 适用: 人, 小鼠 ELISA, WB, ICC, IF 宿主: 兔 Polyclonal unconjugated
anti-FAST Kinase Domains 1 (FASTKD1) antibodyFASTKD1 适用: 人 WB, ICC, IF 宿主: 兔 Polyclonal unconjugated
anti-FAST Kinase Domains 1 (FASTKD1) (Internal Region) antibodyFASTKD1 适用: 人, 小鼠, 猴 ELISA, WB 宿主: 兔 Polyclonal unconjugated
anti-FAST Kinase Domains 1 (FASTKD1) (AA 561-610) antibodyFASTKD1 适用: 人, 小鼠 ELISA, WB, IHC, IHC (p) 宿主: 兔 Polyclonal unconjugated
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- 应用备注
- IHC 1:100-1:300
- 限制
- 仅限研究用
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- 状态
- Liquid
- 浓度
- 0.5 mg/mL
- 缓冲液
- PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
- 储存液
- Sodium azide
- 注意事项
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- 储存条件
- -20 °C
- 储存方法
- Store at -20°C. Avoid freeze / thaw cycles.
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- 抗原
- FASTKD1 (FAST Kinase Domains 1 (FASTKD1))
- 别名
- FASTKD1 (FASTKD1 产品)
- 别名
- zgc:77397 antibody, fakd1 antibody, 5330408N05Rik antibody, mKIAA1800 antibody, RGD1563531 antibody, FAST kinase domains 1 antibody, FAST kinase domain-containing protein 1 antibody, FAST kinase domains 1 L homeolog antibody, fastkd1 antibody, fakd1 antibody, FASTKD1 antibody, Fastkd1 antibody, fastkd1.L antibody
- 背景
- The second largest human chromosome, 2 consists of 237 million bases encoding over 1,400 genes and making up approximately 8 % of the human genome. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstrm syndrome is due to mutations in the ALMS1 gene. Interestingly, chromosome 2 contains what appears to be a vestigial second centromere and vestigial telomeres which gives credence to the hypothesis that human chromosome 2 is the result of an ancient fusion of two ancestral chromosomes seen in modern form today in apes.
- UniProt
- Q53R41
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