RP1 抗体 (AA 451-550)
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- 抗原 See all RP1 抗体
- RP1 (Retinitis Pigmentosa 1 (Autosomal Dominant) (RP1))
- 抗原表位
- AA 451-550
- 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 RP1 antibody is un-conjugated
- 应用范围
- Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), ELISA, Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunocytochemistry (ICC)
- 预测反应
- Human,Mouse,Rat,Dog,Horse,Rabbit
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human RP1/Oxygen-regulated protein 1
- 亚型
- IgG
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- 应用备注
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ELISA 1:500-1000
IHC-P 1:200-400
IHC-F 1:100-500
IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200
ICC 1:100-500 - 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
- RP1 (Retinitis Pigmentosa 1 (Autosomal Dominant) (RP1))
- 别名
- Oxygen-regulated protein 1 (RP1 产品)
- 别名
- orp1 antibody, MGC83581 antibody, DCDC4A antibody, ORP1 antibody, Rp1h antibody, Dcdc3 antibody, Orp1 antibody, mG145 antibody, RP1, axonemal microtubule associated L homeolog antibody, RP1, axonemal microtubule associated antibody, retinitis pigmentosa 1 (autosomal dominant) antibody, uncharacterized LOC100355685 antibody, retinitis pigmentosa 1 (human) antibody, rp1.L antibody, RP1 antibody, rp1 antibody, LOC100355685 antibody, Rp1 antibody
- 背景
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Synonyms: DCDC4A, ORP1, Oxygen-regulated protein 1, Retinitis pigmentosa 1 protein, Retinitis pigmentosa RP1 protein, RP1, RP1_HUMAN.
Background: Retinitis pigmentosa 1 is a novel 2,156 amino acid oxygen-regulated photoreceptor specific to retina. Originally named ORP1 (for 'oxygen-regulated protein-1'), the expression of retinitis pigmentosa 1 has been found to be regulated by oxygen levels in the retina. Mutation of the retinitis pigmentosa 1 gene causes dominant retinitis pigmentosa which leads to degeneration of retinal photoreceptor cells and symptoms such as night vision blindness and deficits in the midperipheral visual field. Retinitis pigmentosa 1 may assist in differentiation of photoreceptor cells and has been identified in the cilia of photoreceptors, possibly aiding in both cilial structure and protein transport between inner and outer segments of photoreceptors. Retinitis pigmentosa 1 contains two doublecortin domains and is encoded by a gene which maps to human chromosome 8q11-q13.
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