METTL7A 抗体
Quick Overview for METTL7A 抗体 (ABIN7264251)
抗原
See all METTL7A 抗体适用
宿主
克隆类型
标记
应用范围
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产品特性
- Polyclonal Antibody
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纯化方法
- Affinity purification
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免疫原
- Recombinant fusion protein of human METTL7A (NP_054752.3).
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亚型
- IgG
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anti-Methyltransferase Like 7A (METTL7A) (AA 30-244) antibody
METTL7A 适用: 人 WB, IHC, IF 宿主: 兔 Polyclonal unconjugated
anti-Methyltransferase Like 7A (METTL7A) (Internal Region) antibodyMETTL7A 适用: 人, 小鼠 ELISA, WB, IHC, ICC, IHC (p) 宿主: 兔 Polyclonal unconjugated
anti-Methyltransferase Like 7A (METTL7A) (AA 30-244) antibodyMETTL7A 适用: 人 ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-Methyltransferase Like 7A (METTL7A) (AA 1-244) antibodyMETTL7A 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
anti-Methyltransferase Like 7A (METTL7A) (AA 51-100) antibodyMETTL7A 适用: 人, 小鼠, 大鼠, Cow, Hamster, 猴 WB 宿主: 兔 Polyclonal unconjugated
anti-Methyltransferase Like 7A (METTL7A) (N-Term) antibodyMETTL7A 适用: 人, 大鼠 WB 宿主: 兔 Polyclonal unconjugated
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应用备注
- WB 1:500-1:2000 IHC 1:50-1:200
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限制
- 仅限研究用
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状态
- Liquid
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浓度
- 1 mg/mL
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缓冲液
- PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
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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
- Store at -20°C. Avoid freeze / thaw cycles.
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- METTL7A (Methyltransferase Like 7A (METTL7A))
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别名
- METTL7A
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背景
- METTL7A (methyltransferase like 7A), also known as AAM-B, is a 244 amino acid protein that is thought to function as a methyltransferase and is encoded by a gene which maps to chromosome 12. Encoding over 1,100 genes, chromosome 12 comprises nearly 4.5 % of the human genome and is associated with a number of skeletal deformaties, including hypochondrogenesis, achondrogenesis and Kniest dysplasia. Chromosome 12 is also home to both a homeobox gene cluster which encodes crucial transcription factors for morphogenesis, and a natural killer complex gene cluster encoding C-type lectin proteins which mediate the NK cell response to MHC I interaction. Additionally, Trisomy 12p (three copies of the p arm of chromosome 12) leads to facial developmental defects, seizure disorders and a host of other symptoms varying in severity depending on the extent of mosaicism.
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分子量
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Observed_MW: 28 kDa
Calculated_MW: 28 kDa
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基因ID
- 25840
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UniProt
- Q9H8H3
抗原
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