MAGE-Like 2 抗体
Quick Overview for MAGE-Like 2 抗体 (ABIN2433343)
抗原
See all MAGE-Like 2 (MAGEL2) 抗体适用
宿主
克隆类型
标记
应用范围
-
-
纯化方法
- Antigen affinity purification
-
免疫原
- Synthetic peptide of human MAGEL2
-
亚型
- IgG
-
-
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) (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, Cow, 犬, Pig, 兔 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
-
-
应用备注
- Optimal working dilution should be determined by the investigator.
-
限制
- 仅限研究用
-
-
-
状态
- Liquid
-
注意事项
- Avoid freeze / thaw cycles.
-
储存条件
- -20 °C/-80 °C
-
储存方法
- Store at -20°C (regular) and -80°C (long term).
-
-
- MAGE-Like 2 (MAGEL2)
-
别名
- MAGEL2
-
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: PWLS, nM15, NDNL1 -
分子量
- Calculated MW: 59 kDa
抗原
-
