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TMEM244 抗体

TMEM244 适用: 人 WB, IF (p), IHC (p) 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN1715075
发货至: 中国
  • 抗原 See all TMEM244 products
    TMEM244 (Transmembrane Protein 244 (TMEM244))
    适用
    宿主
    • 14
    克隆类型
    • 14
    多克隆
    标记
    • 1
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    This TMEM244 antibody is un-conjugated
    应用范围
    Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
    交叉反应
    纯化方法
    Purified by Protein A.
    免疫原
    KLH conjugated synthetic peptide derived from human C6orf191
    亚型
    IgG
  • 应用备注
    WB 1:100-1000
    IHC-P 1:100-500
    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 1 % BSA, 50 % glycerol and 0.09 % sodium azide.
    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 for 12 months.
    有效期
    12 months
  • 抗原
    TMEM244 (Transmembrane Protein 244 (TMEM244))
    别名
    C6orf191 (TMEM244 产品)
    别名
    C6orf191 antibody, bA174C7.4 antibody, transmembrane protein 244 antibody, TMEM244 antibody
    背景

    Synonyms: bA174C7.4, C6orf191, TM244_HUMAN, Chromosome 6 open reading frame 191, Putative transmembrane protein C6orf191.

    Background: Making up nearly 6 % of the human genome, chromosome 6 contains around 1,200 genes within 170 million base pairs of sequence. Deletion of a portion of the q arm of chromosome 6 is associated with early onset intestinal cancer suggesting the presence of a cancer susceptibility locus. Porphyria cutanea tarda is associated with chromosome 6 through the HFE gene which, when mutated, predisposes an individual to developing this porphyria. Notably, the PARK2 gene, which is associated with Parkinson's disease, and the genes encoding the major histocompatiblity complex proteins, which are key molecular components of the immune system and determine predisposition to rheumatic diseases, are also located on chromosome 6. Stickler syndrome, 21-hydroxylase deficiency and maple syrup urine disease are also associated with genes on chromosome 6. A bipolar disorder susceptibility locus has been identified on the q arm of chromosome 6. The C6orf191 gene product has been provisionally designated C6orf191 pending further characterization.

    基因ID
    253582
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