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LURAP1L 抗体 (AbBy Fluor® 555)

LURAP1L 适用: 人, 小鼠, 大鼠 WB, IF (p) 宿主: 兔 Polyclonal AbBy Fluor® 555
产品编号 ABIN1403057
发货至: 中国
  • 抗原 See all LURAP1L products
    LURAP1L (Leucine Rich Adaptor Protein 1-Like (LURAP1L))
    适用
    人, 小鼠, 大鼠
    宿主
    • 21
    克隆类型
    • 21
    多克隆
    标记
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This LURAP1L antibody is conjugated to AbBy Fluor® 555
    应用范围
    • 21
    • 12
    • 7
    • 7
    • 6
    • 4
    Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
    交叉反应
    人, 小鼠, 大鼠
    纯化方法
    Purified by Protein A.
    免疫原
    KLH conjugated synthetic peptide derived from human C9orf150
    亚型
    IgG
  • 应用备注
    IF(IHC-P) 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
    LURAP1L (Leucine Rich Adaptor Protein 1-Like (LURAP1L))
    别名
    C9orf150 (LURAP1L 产品)
    别名
    C9orf150 antibody, bA3L8.2 antibody, RGD1308059 antibody, 1110029A09Rik antibody, AV077978 antibody, AV175137 antibody, D4Bwg0951e antibody, WI-13707 antibody, bM350F23.1 antibody, leucine rich adaptor protein 1 like antibody, leucine rich adaptor protein 1-like antibody, LURAP1L antibody, Lurap1l antibody
    背景

    Synonyms: LURAP1L, bA3L8.2, FLJ38505, C9orf150, Chromosome 9 open reading frame 150, CI150_HUMAN, FLJ90271, HYST0841, MGC46502, Uncharacterized protein C9orf150.

    Background: C9orf150 is a 231 amino acid protein encoded by a gene that maps to human chromosome 9p23. Chromosome 9 consists of about 145 million bases, represents 4 % of the human genome and encodes nearly 900 genes. Thought 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.

    基因ID
    286343
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