RAX2 抗体
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北京 101111
Quick Overview for RAX2 抗体 (ABIN7466343)
抗原
See all RAX2 抗体适用
宿主
克隆类型
标记
应用范围
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交叉反应
- 人
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纯化方法
- Purified by antigen-affinity chromatography.
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免疫原
- Recombinant protein encompassing a sequence within the center region of human RAX2. The exact sequence is proprietary.
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亚型
- IgG
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anti-Retina and Anterior Neural Fold Homeobox 2 (RAX2) (AA 1-184) antibody
RAX2 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
anti-Retina and Anterior Neural Fold Homeobox 2 (RAX2) (N-Term) antibodyRAX2 适用: 人, 犬 WB 宿主: 兔 Polyclonal unconjugated
anti-Retina and Anterior Neural Fold Homeobox 2 (RAX2) (AA 1-168) antibodyRAX2 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
anti-Retina and Anterior Neural Fold Homeobox 2 (RAX2) (N-Term) antibodyRAX2 适用: 人, 犬, Cow, Pig WB 宿主: 兔 Polyclonal unconjugated
anti-Retina and Anterior Neural Fold Homeobox 2 (RAX2) antibodyRAX2 适用: 人 WB, ELISA 宿主: 兔 Polyclonal unconjugated
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应用备注
- WB: 1:500-1:3000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.
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说明
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Positive Control: IMR32
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限制
- 仅限研究用
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状态
- Liquid
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浓度
- 0.86 mg/mL
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缓冲液
- 0.1M Tris-Glycine ( pH 7), 20 % Glycerol, 0.01 % Thimerosal
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储存液
- Thimerosal (Merthiolate)
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注意事项
- This product contains Thimerosal (Merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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储存条件
- 4 °C,-20 °C
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储存方法
- Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
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- RAX2 (Retina and Anterior Neural Fold Homeobox 2 (RAX2))
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别名
- retina and anterior neural fold homeobox 2
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背景
- Retina and anterior neural fold homeobox 2 , ARMD6 , CORD11 , QRX , RAXL1,This gene encodes a homeodomain-containing protein that plays a role in eye development. Mutation of this gene causes age-related macular degeneration type 6, an eye disorder resulting in accumulations of protein and lipid beneath the retinal pigment epithelium and within the Bruch's membrane. Defects in this gene can also cause cone-rod dystrophy type 11, a disease characterized by the initial degeneration of cone photoreceptor cells and resulting in loss of color vision and visual acuity, followed by the degeneration of rod photoreceptor cells, which progresses to night blindness and the loss of peripheral vision. [provided by RefSeq]
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分子量
- 20 kDa
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基因ID
- 84839
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UniProt
- Q96IS3
抗原
-
