RP2 抗体 (AA 244-348)
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北京 101111
Quick Overview for RP2 抗体 (AA 244-348) (ABIN7872775)
抗原
See all RP2 抗体适用
宿主
克隆类型
标记
应用范围
克隆位点
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抗原表位
- AA 244-348
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原理
- RP2 Antibody
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纯化方法
- Affinity purified
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免疫原
- A human recombinant protein (amino acids D244-M348) was used as the immunogen for the RP2 antibody.
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亚型
- IgG2b
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anti-Retinitis Pigmentosa 2 (X-Linked Recessive) (RP2) (AA 251-350) antibody
RP2 适用: 人 WB, ELISA 宿主: 小鼠 Monoclonal 5C10 unconjugated
anti-Retinitis Pigmentosa 2 (X-Linked Recessive) (RP2) (AA 251-350) antibodyRP2 适用: 人 WB, ELISA, IF 宿主: 小鼠 Monoclonal 1B4 unconjugated
anti-Retinitis Pigmentosa 2 (X-Linked Recessive) (RP2) (AA 1-350) antibodyRP2 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
anti-Retinitis Pigmentosa 2 (X-Linked Recessive) (RP2) (AA 1-350) antibodyRP2 适用: 人 WB, ELISA, IHC, IP 宿主: 兔 Polyclonal unconjugated
anti-Retinitis Pigmentosa 2 (X-Linked Recessive) (RP2) (AA 1-350) antibodyRP2 适用: 人 ELISA, IHC, IF 宿主: 兔 Polyclonal unconjugated
anti-Retinitis Pigmentosa 2 (X-Linked Recessive) (RP2) (C-Term) antibodyRP2 适用: 人, 小鼠, 大鼠, 犬, 兔, Hamster WB, IHC, IHC (p) 宿主: 兔 Polyclonal unconjugated
anti-Retinitis Pigmentosa 2 (X-Linked Recessive) (RP2) (AA 244-348) antibodyRP2 适用: 人, 小鼠, 大鼠 WB, IF, FACS, ICC 宿主: 小鼠 Monoclonal 3D7 unconjugated
anti-Retinitis Pigmentosa 2 (X-Linked Recessive) (RP2) (AA 244-348) antibodyRP2 适用: 人, 小鼠, 大鼠 WB, ELISA, IHC, IF, FACS, ICC 宿主: 兔 Polyclonal unconjugated
anti-Retinitis Pigmentosa 2 (X-Linked Recessive) (RP2) (Middle Region) antibodyRP2 适用: 人, 小鼠, 大鼠, 犬, 兔, Cow, 豚鼠, 马 WB, IHC 宿主: 兔 Polyclonal unconjugated
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应用备注
- Optimal dilution of the RP2 antibody should be determined by the researcher.
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限制
- 仅限研究用
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状态
- Lyophilized
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缓冲液
- 0.5 mg/mL if reconstituted with 0.2 mL sterile DI water
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储存条件
- 4 °C,-20 °C
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储存方法
- After reconstitution, the RP2 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
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- RP2 (Retinitis Pigmentosa 2 (X-Linked Recessive) (RP2))
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别名
- RP2
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背景
- Protein XRP2 is a protein that in humans is encoded by the RP2 gene. It is mapped to Xp11.3. The RP2 locus has been implicated as one cause of X-linked retinitis pigmentosa. The predicted gene product shows homology with human cofactor C, a protein involved in the ultimate step of beta-tubulin folding. Progressive retinal degeneration may therefore be due to the accumulation of incorrectly folded photoreceptor or neuron-specific tubulin isoforms followed by progressive cell death.The RP2 protein is also involved in regulating the function and extension of outer segment of cone photoreceptors in mice.
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UniProt
- O75695
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途径
- Nucleotide Phosphorylation, Ribonucleoside Biosynthetic Process
抗原
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