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C9orf6 抗体 (AA 1-100) (Alexa Fluor 594)

FAM206A 适用: 大鼠 IF (cc), IF (p) 宿主: 兔 Polyclonal Alexa Fluor 594
产品编号 ABIN2810980
发货至: 中国
  • 抗原 See all C9orf6 (FAM206A) 抗体
    C9orf6 (FAM206A) (Family with Sequence Similarity 206, Member A (FAM206A))
    抗原表位
    • 14
    • 1
    • 1
    AA 1-100
    适用
    • 14
    • 2
    大鼠
    宿主
    • 14
    • 2
    克隆类型
    • 16
    多克隆
    标记
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This C9orf6 antibody is conjugated to Alexa Fluor 594
    应用范围
    • 12
    • 12
    • 3
    • 3
    • 3
    • 2
    • 2
    • 1
    Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
    交叉反应
    大鼠
    预测反应
    Human,Mouse,Dog,Cow,Sheep,Pig,Horse
    纯化方法
    Purified by Protein A.
    免疫原
    KLH conjugated synthetic peptide derived from human C9orf6
    亚型
    IgG
    Top Product
    Discover our top product FAM206A Primary Antibody
  • 应用备注
    IF(IHC-P) 1:50-200
    IF(IHC-F) 1:50-200
    IF(ICC) 1:50-200
    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    1 μg/μL
    缓冲液
    Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
    储存液
    ProClin
    注意事项
    This product contains ProClin: 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. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
    有效期
    12 months
  • 抗原
    C9orf6 (FAM206A) (Family with Sequence Similarity 206, Member A (FAM206A))
    别名
    C9orf6 (FAM206A 产品)
    别名
    Fam206a antibody, C9orf6 antibody, CG-8 antibody, C8H9orf6 antibody, C2H9orf6 antibody, si:ch211-254e15.2 antibody, zgc:153072 antibody, family with sequence similarity 206, member A antibody, family with sequence similarity 206 member A antibody, Fam206a antibody, FAM206A antibody, fam206a antibody
    背景

    Synonyms: CG 8, CG8, FLJ20457, Hypothetical protein LOC54942, UPF0436 protein C9orf6, F206A_HUMAN.

    Background: Chromosome 9 consists of about 145 million bases and 4 % of the human genome and encodes nearly 900 genes. Considered to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias. The C9orf6 gene product has been provisionally designated C9orf6 pending further characterization.

    基因ID
    54942
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