CA8 抗体 (full length)
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北京 101111
Quick Overview for CA8 抗体 (full length) (ABIN7877772)
抗原
See all CA8 抗体适用
宿主
克隆类型
标记
应用范围
质量等级
克隆位点
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抗原表位
- full length
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原理
- Carbonic Anhydrase VIII Antibody / CA8 (azide and preservative free)
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纯化方法
- Protein A/G affinity
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免疫原
- Recombinant full-length human Carbonic Anhydrase VIII/CA8 protein was used as the immunogen for the Carbonic Anhydrase VIII antibody.
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亚型
- IgG2a, kappa
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anti-Carbonic Anhydrase VIII (CA8) antibody
CA8 适用: 人 WB, IHC 宿主: 小鼠 Monoclonal CPTC-CA8-2 unconjugated
anti-Carbonic Anhydrase VIII (CA8) (AA 40-139) antibodyCA8 适用: 人 WB, ELISA 宿主: 小鼠 Monoclonal 1F7 unconjugated
anti-Carbonic Anhydrase VIII (CA8) (AA 1-290) antibodyCA8 适用: 人 WB, IHC, ELISA 宿主: 兔 Polyclonal unconjugated
anti-Carbonic Anhydrase VIII (CA8) (N-Term) antibodyCA8 适用: 人, 小鼠, 大鼠, 犬, 斑马鱼 WB 宿主: 兔 Polyclonal unconjugated
anti-Carbonic Anhydrase VIII (CA8) (AA 31-80) antibodyCA8 适用: 人, 小鼠, 大鼠, Cow, 犬, 斑马鱼, 猴, 豚鼠, 马, 兔, Bat, 小鸡, Pig WB 宿主: 兔 Polyclonal unconjugated
anti-Carbonic Anhydrase VIII (CA8) (C-Term) antibodyCA8 适用: 人, 小鼠, 大鼠 WB, ELISA 宿主: 兔 Polyclonal unconjugated
anti-Carbonic Anhydrase VIII (CA8) (AA 40-139) antibodyCA8 适用: 人 WB, ELISA 宿主: 小鼠 Polyclonal unconjugated
anti-Carbonic Anhydrase VIII (CA8) (C-Term) antibodyCA8 适用: 人, 小鼠, 大鼠, Cow, 犬, 斑马鱼, 猴, 豚鼠, 马, 兔, Bat, 小鸡, Pig WB 宿主: 兔 Polyclonal unconjugated
anti-Carbonic Anhydrase VIII (CA8) antibodyCA8 适用: 人 WB 宿主: 小鼠 Monoclonal 25GB8390 unconjugated
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应用备注
- Optimal dilution of the Carbonic Anhydrase VIII antibody should be determined by the researcher.
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限制
- 仅限研究用
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状态
- Liquid
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浓度
- 1 mg/mL
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缓冲液
- 1 mg/mL in 1X PBS, BSA free, sodium azide free
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储存液
- Azide free
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储存条件
- -20 °C
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储存方法
- Aliquot the Carbonic Anhydrase VIII antibody and store frozen at -20oC or colder. Avoid repeated freeze-thaw cycles.
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- CA8 (Carbonic Anhydrase VIII (CA8))
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别名
- Carbonic Anhydrase VIII
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背景
- Carbonic anhydrase-related protein is an protein that in humans is encoded by the CA8 gene. The CA8 protein lacks the catalytic activity of other carbonic anhydrase enzymes. A rare, autosomal recessive form of cerebellar ataxia known as cerebellar ataxia, mental retardation, and dysequilibrium syndrome 3 (CAMRQ3) is caused by mutations in the CA8 gene. [Wiki]
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UniProt
- P35219
抗原
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