MAGE-Like 2 抗体 (N-Term)
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- 抗原 See all MAGE-Like 2 (MAGEL2) 抗体
- MAGE-Like 2 (MAGEL2)
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抗原表位
- N-Term
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适用
- 人, Cow, 犬, Pig, 兔
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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 MAGE-Like 2 antibody is un-conjugated
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应用范围
- Western Blotting (WB)
- 序列
- MQGLFYRPQG SSKERRTSSK ERRAPSKDRM IFAATFCAPK AVSAARAHLP
- 预测反应
- Cow: 83%, Dog: 100%, Human: 100%, Pig: 88%, Rabbit: 100%
- 产品特性
- This is a rabbit polyclonal antibody against MAGEL2. It was validated on Western Blot.
- 纯化方法
- Affinity Purified
- 免疫原
- The immunogen is a synthetic peptide directed towards the N terminal region of human MAGEL2
- Top Product
- Discover our top product MAGEL2 Primary Antibody
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anti-MAGE-Like 2 (MAGEL2) antibody
MAGEL2 适用: 人 ELISA, WB 宿主: 兔 Polyclonal unconjugated
anti-MAGE-Like 2 (MAGEL2) (N-Term) antibodyMAGEL2 适用: 人, Cow, 犬, Pig, 兔, 猴 WB 宿主: 兔 Polyclonal unconjugated
anti-MAGE-Like 2 (MAGEL2) antibodyMAGEL2 适用: 人, 小鼠, 大鼠 ELISA, WB 宿主: 兔 Polyclonal unconjugated
anti-MAGE-Like 2 (MAGEL2) (AA 499-529), (C-Term) antibodyMAGEL2 适用: 人 WB, IHC (p) 宿主: 兔 Polyclonal RB2131 unconjugated
anti-MAGE-Like 2 (MAGEL2) (N-Term) antibodyMAGEL2 适用: 人 WB, IHC (p), EIA 宿主: 兔 Polyclonal unconjugated
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- 应用备注
- Optimal working dilutions should be determined experimentally by the investigator.
- 说明
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Antigen size: 529 AA
- 限制
- 仅限研究用
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- 状态
- Liquid
- 浓度
- Lot specific
- 缓冲液
- Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.
- 储存液
- Sodium azide
- 注意事项
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- 注意事项
- Avoid repeated freeze-thaw cycles.
- 储存条件
- -20 °C
- 储存方法
- For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
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- 抗原
- MAGE-Like 2 (MAGEL2)
- 别名
- MAGEL2 (MAGEL2 产品)
- 别名
- NDNL1 antibody, nM15 antibody, MAGEL2 antibody, Mage-l2 antibody, ns7 antibody, MAGE family member L2 antibody, melanoma antigen, family L, 2 antibody, MAGEL2 antibody, Magel2 antibody
- 背景
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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.
Alias Symbols: NDNL1, nM15
Protein Interaction Partner: VPS35, VPS26A, USP7, TRIM27, UBC,
Protein Size: 529 - 分子量
- 58 kDa
- 基因ID
- 54551
- NCBI登录号
- NM_019066
- UniProt
- Q9UJ55
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