MAGE-Like 2 抗体 (AA 578-847)
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北京 101111
Quick Overview for MAGE-Like 2 抗体 (AA 578-847) (ABIN8007361)
抗原
See all MAGE-Like 2 (MAGEL2) 抗体适用
宿主
克隆类型
标记
应用范围
质量等级
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抗原表位
- AA 578-847
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原理
- Anti-MAGEL2 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-MAGEL2 Antibody. Tested in ELISA, IHC, WB, Flow Cytometry applications. This antibody reacts with Human.
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纯化方法
- Immunogen affinity purified.
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免疫原
- E.coli-derived human MAGEL2 recombinant protein (Position: Q578-A847).
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亚型
- IgG
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应用备注
- Western blot, 0.25-0.5 μg/mL, Human Immunohistochemistry (Paraffin-embedded Section), 2-5 μg/mL, Human Flow Cytometry (Fixed), 1-3 μg/1x106 cells, Human ELISA, 0.1-0.5 μg/mL, -
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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. -
有效期
- 12 months
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- MAGE-Like 2 (MAGEL2)
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别名
- MAGEL2
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背景
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Background: Prader-Willi syndrome (PWS) is caused by the loss of expression of imprinted genes in chromosome 15q11-q13 region. Affected individuals exhibit neonatal hypotonia, developmental delay, and childhood-onset obesity. Necdin (NDN), a gene involved in the terminal differentiation of neurons, localizes to this region of the genome and has been implicated as one of the genes responsible for the etiology of PWS. This gene is structurally similar to NDN, is also localized to the PWS chromosomal region, and is paternally imprinted, suggesting a possible role for it in PWS.
Gene Full Name: MAGE family member L2
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分子量
- 133 kDa
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基因ID
- 54551
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UniProt
- Q9UJ55
抗原
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