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METTL7A 抗体

METTL7A 适用: 人, 大鼠 WB, IHC 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN6571617
发货至: 中国
  • 抗原 See all METTL7A 抗体
    METTL7A (Methyltransferase Like 7A (METTL7A))
    适用
    • 28
    • 6
    • 4
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    人, 大鼠
    宿主
    • 27
    • 1
    克隆类型
    • 28
    多克隆
    标记
    • 13
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This METTL7A antibody is un-conjugated
    应用范围
    • 15
    • 12
    • 10
    • 3
    • 2
    • 1
    • 1
    • 1
    Western Blotting (WB), Immunohistochemistry (IHC)
    纯化方法
    Affinity purification
    免疫原
    Recombinant fusion protein of human METTL7A (NP_054752.3).
    亚型
    IgG
    Top Product
    Discover our top product METTL7A Primary Antibody
  • 应用备注
    WB 1:500-1:2000 IHC 1:50-1:200
    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    1 mg/mL
    缓冲液
    PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
    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.
    储存条件
    -20 °C
    储存方法
    Store at -20°C. Avoid freeze / thaw cycles.
  • 抗原
    METTL7A (Methyltransferase Like 7A (METTL7A))
    别名
    METTL7A (METTL7A 产品)
    别名
    AAM-B antibody, 2210414H16Rik antibody, 3300001H21Rik antibody, Aam-B antibody, Mettl7a antibody, UbiE1 antibody, RGD1308407 antibody, MGC82719 antibody, zgc:153889 antibody, MGC145311 antibody, DKFZp459L026 antibody, methyltransferase like 7A antibody, methyltransferase like 7A1 antibody, methyltransferase like 7A L homeolog antibody, METTL7A antibody, Mettl7a1 antibody, Mettl7a antibody, mettl7a.L antibody, mettl7a antibody
    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.
    分子量

    Observed_MW: 28kDa

    Calculated_MW: 28kDa

    基因ID
    25840
    UniProt
    Q9H8H3
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