RAX2 抗体 (C-Term)
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Quick Overview for RAX2 抗体 (C-Term) (ABIN7602913)
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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抗原表位
- C-Term
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原理
- Anti-RAX2 Antibody
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交叉反应 （详细）
- No cross-reactivity with other proteins.
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产品特性
- Anti-RAX2 Antibody (ABIN7602913). Tested in IHC, WB applications. This antibody reacts with Human. This is a premium antibody that guarantees superior quality, high affinity, and strong signals with minimal background in Western blot applications.
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纯化方法
- Immunogen affinity purified.
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免疫原
- A synthetic peptide corresponding to a sequence at the C-terminus of human RAX2.
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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
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Western blot, 0.1-0.25 μg/mL, Human
Immunohistochemistry(Paraffin-embedded Section), 2-5 μg/mL, Human
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限制
- 仅限研究用
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状态
- Lyophilized
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溶解方式
- Adding 0.2 mL of distilled water will yield a concentration of 500 μg/mL.
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浓度
- 500 μg/mL
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缓冲液
- Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4.
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储存条件
- 4 °C,-20 °C
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储存方法
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At -20°C for one year from date of receipt. After reconstitution, at 4°C for one month.
It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freezing and thawing.
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- RAX2 (Retina and Anterior Neural Fold Homeobox 2 (RAX2))
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别名
- RAX2
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背景
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Synonyms: RNA-binding protein Nova-2, Astrocytic NOVA1-like RNA-binding protein, Neuro-oncological ventral antigen 2, NOVA2, ANOVA, NOVA3
Tissue Specificity: Brain. Expression restricted to astrocytes.
Background: 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. Alternative splicing results in multiple transcript variants.
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分子量
- 18 kDa
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基因ID
- 84839
抗原
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