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CMSS1 抗体 (AbBy Fluor® 750)

CMSS1 适用: 人, 大鼠, 小鼠 WB 宿主: 兔 Polyclonal AbBy Fluor® 750
产品编号 ABIN4998444
发货至: 中国
  • 抗原 See all CMSS1 抗体
    CMSS1 (Cms Small Ribosomal Subunit 1 (CMSS1))
    适用
    • 16
    • 12
    • 12
    • 1
    • 1
    • 1
    人, 大鼠, 小鼠
    宿主
    • 16
    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 CMSS1 antibody is conjugated to AbBy Fluor® 750
    应用范围
    • 16
    • 3
    Western Blotting (WB)
    交叉反应
    预测反应
    Mouse,Rat,Horse
    纯化方法
    Purified by Protein A.
    免疫原
    KLH conjugated synthetic peptide derived from human C3orf26
    亚型
    IgG
    Top Product
    Discover our top product CMSS1 Primary Antibody
  • 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
    CMSS1 (Cms Small Ribosomal Subunit 1 (CMSS1))
    别名
    C3orf26 (CMSS1 产品)
    别名
    C3orf26 antibody, 1110001A06Rik antibody, 2610528E23Rik antibody, 4930572F24Rik antibody, AV099812 antibody, AV122629 antibody, RGD1309437 antibody, c3orf26 antibody, C1H3orf26 antibody, cms1 ribosomal small subunit homolog (yeast) antibody, cms small ribosomal subunit 1 antibody, cms1 ribosomal small subunit homolog L homeolog antibody, CMSS1 antibody, Cmss1 antibody, cmss1.L antibody
    背景

    Synonyms: C3orf26, CC026_HUMAN, MGC4308, Uncharacterized protein C3orf26.

    Background: Chromosome 3 is made up of about 214 million bases encoding over 1,100 genes. Notably, there is a chemokine receptor gene cluster and a variety of human cancer related loci on chromosome 3. Particular regions of the chromosome 3 short arm are deleted in many types of cancer cells. Key tumor suppressing genes on chromosome 3 encode apoptosis mediator RASSF1, cell migration regulator HYAL1 and angiogenesis suppressor SEMA3B. Marfan Syndrome, porphyria, von Hippel-Lindau syndrome, osteogenesis imperfecta and Charcot-Marie-Tooth Disease are a few of the numerous genetic diseases associated with chromosome 3. The C3orf26 gene product has been provisionally designated C3orf26 pending further characterization.

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