RP2 抗体 (AA 244-348) (Cy3)
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北京 101111
Quick Overview for RP2 抗体 (AA 244-348) (Cy3) (ABIN8031719)
抗原
See all RP2 抗体适用
宿主
克隆类型
标记
应用范围
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抗原表位
- AA 244-348
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原理
- Anti-RP2 Antibody Cy3 Conjugated
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特异性
- No cross reactivity with other proteins.
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交叉反应 （详细）
- No cross-reactivity with other proteins.
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纯化方法
- Immunogen affinity purified.
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免疫原
- E. coli-derived human RP2 recombinant protein (Position: D244-M348).
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亚型
- IgG
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anti-Retinitis Pigmentosa 2 (X-Linked Recessive) (RP2) (AA 244-348) antibody
RP2 适用: 人, 小鼠, 大鼠 WB, ELISA, FACS, IHC, IF, ICC 宿主: 兔 Polyclonal unconjugated
anti-Retinitis Pigmentosa 2 (X-Linked Recessive) (RP2) (AA 251-350) antibodyRP2 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, FACS, IF, ICC 宿主: 小鼠 Monoclonal 3D7 unconjugated
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应用备注
- Flow Cytometry, 1-3 μg/1x106 cells
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限制
- 仅限研究用
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状态
- Liquid
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缓冲液
- Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4, 0.02 % Sodium azide.
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储存液
- Sodium azide
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注意事项
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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储存条件
- -20 °C
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储存方法
- At -20°C for one year from date of receipt. Avoid repeated freezing and thawing. Protect from light.
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有效期
- 12 months
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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
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Background: 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.
Gene Full Name: RP2 activator of ARL3 GTPase
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基因ID
- 6102
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UniProt
- O75695
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途径
- Nucleotide Phosphorylation, Ribonucleoside Biosynthetic Process
抗原
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