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C5ORF4 抗体 (AA 98-134) (Alexa Fluor 555)

FAXDC2 适用: 人, 大鼠, 小鼠 WB, IF (p) 宿主: 兔 Polyclonal Alexa Fluor 555
产品编号 ABIN1402973
发货至: 中国
  • 抗原 See all C5ORF4 (FAXDC2) products
    C5ORF4 (FAXDC2) (Fatty Acid Hydroxylase Domain Containing 2 (FAXDC2))
    抗原表位
    • 14
    • 2
    • 1
    AA 98-134
    适用
    • 19
    • 15
    • 14
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    人, 大鼠, 小鼠
    宿主
    • 19
    克隆类型
    • 19
    多克隆
    标记
    • 6
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This C5ORF4 antibody is conjugated to Alexa Fluor 555
    应用范围
    • 19
    • 12
    • 4
    • 4
    • 2
    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 C5ORF4
    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
    C5ORF4 (FAXDC2) (Fatty Acid Hydroxylase Domain Containing 2 (FAXDC2))
    别名
    C5ORF4 (FAXDC2 产品)
    别名
    C5orf4 antibody, fatty acid hydroxylase domain containing 2 antibody, FAXDC2 antibody
    背景

    Synonyms: Hypothetical protein LOC10826, Chromosome 5 open reading frame 4, FLJ13758, CE004_HUMAN.

    Background: With 181 million base pairs encoding around 1,000 genes, chromosome 5 is about 6 % of human genomic DNA. It is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is also chromosome 5 associated and is caused by insertions or deletions within the TCOF1 gene. Deletion of the p arm of chromosome 5 leads to Cri du chat syndrome. Deletion of 5q or chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome. The C5orf4 gene product has been provisionally designated C5orf4 pending further characterization.

    基因ID
    10826
    UniProt
    Q96IV6
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