RAX2 抗体 (C-Term) (Biotin)
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Quick Overview for RAX2 抗体 (C-Term) (Biotin) (ABIN8031685)
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 Biotin Conjugated
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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
- 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) (C-Term) antibody
RAX2 适用: 人 WB, IHC 宿主: 兔 Polyclonal unconjugated
anti-Retina and Anterior Neural Fold Homeobox 2 (RAX2) (AA 1-184) antibodyRAX2 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) antibodyRAX2 适用: 人 WB, ELISA 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
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应用备注
- Western blot, Optimal dilutions should be determined by end users. Immunohistochemistry (Paraffin-embedded Section), Optimal dilutions should be determined by end users. ELISA, Optimal dilutions should be determined by end users.
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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.
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有效期
- 12 months
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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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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.
Gene Full Name: retina and anterior neural fold homeobox 2
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基因ID
- 84839
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UniProt
- Q96IS3
抗原
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