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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
- C-Term
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适用
- 人
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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)
- 纯化方法
- Purified
- 免疫原
- MAGEL2 antibody was raised in rabbit using the C terminal of MAGEL2 as the immunogen
- Top Product
- Discover our top product MAGEL2 Primary Antibody
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anti-MAGE-Like 2 (MAGEL2) (C-Term) antibody
MAGEL2 适用: 人 ELISA, WB, IHC (p) 宿主: 兔 Polyclonal unconjugated
anti-MAGE-Like 2 (MAGEL2) antibodyMAGEL2 适用: 人 ELISA, WB 宿主: 兔 Polyclonal unconjugated
anti-MAGE-Like 2 (MAGEL2) antibodyMAGEL2 适用: 人 ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-MAGE-Like 2 (MAGEL2) (N-Term) antibodyMAGEL2 适用: 人, 兔, Cow, 犬, Pig, 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, 兔, Cow, 犬, Pig WB 宿主: 兔 Polyclonal 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
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WB: 0.2-1 µg/mL
Optimal conditions should be determined by the investigator. - 说明
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MAGEL2 Blocking Peptide, catalog no. 33R-6559, is also available for use as a blocking control in assays to test for specificity of this MAGEL2 antibody
- 限制
- 仅限研究用
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- 状态
- Lyophilized
- 浓度
- Lot specific
- 缓冲液
- Lyophilized powder. Add 50 µL of distilled water. Final antibody concentration is 1 mg/mL in PBS buffer.
- 注意事项
- Avoid repeated freeze/thaw cycles.
- 储存条件
- 4 °C/-20 °C
- 储存方法
- Store at 4 °C, following reconstitution, aliquot and store at -20 °C.
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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
- 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. Synonyms: Polyclonal MAGEL2 antibody, Anti-MAGEL2 antibody, MAGE-like 2 antibody, NDNL1 antibody, nM15 antibody.
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