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PUS7L 抗体 (AA 165-699) (Fluoro488)

This 兔 多克隆 antibody specifically detects PUS7L in FACS. It exhibits reactivity toward 人, 小鼠 和 大鼠.
产品编号 ABIN8028848
发货至: 中国
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Quick Overview for PUS7L 抗体 (AA 165-699) (Fluoro488) (ABIN8028848)

抗原

PUS7L (Pseudouridylate Synthase 7 Homolog-Like (PUS7L))

适用

人, 小鼠, 大鼠

宿主

  • 17
  • 2

克隆类型

  • 19
多克隆

标记

  • 10
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This PUS7L antibody is conjugated to Fluoro488

应用范围

  • 12
  • 7
  • 6
  • 5
  • 3
  • 2
  • 1
Flow Cytometry (FACS)
  • 抗原表位

    • 12
    • 2
    • 1
    • 1
    • 1
    AA 165-699

    原理

    Anti-PUS7L Antibody Fluoro488 Conjugated

    交叉反应 (详细)

    No cross-reactivity with other proteins

    纯化方法

    Immunogen affinity purified.

    免疫原

    E.coli-derived human PUS7L recombinant protein (Position: R165-H699).

    亚型

    IgG
  • 应用备注

    Flow Cytometry, Optimal dilutions should be determined by end users.

    限制

    仅限研究用
  • 状态

    Liquid

    缓冲液

    Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4, 0.02 % 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

    At -20°C for one year from date of receipt. Avoid repeated freezing and thawing. Protect from light.

    有效期

    12 months
  • 抗原

    PUS7L (Pseudouridylate Synthase 7 Homolog-Like (PUS7L))

    别名

    PUS7L

    背景

    Background: Pseudouridylate synthase 7 homolog-like protein is an enzyme that in humans is encoded by the PUS7L gene. PUS7L (pseudouridylate synthase 7 homolog (S. cerevisiae) -like) is a 701 amino acid protein that belongs to the pseudouridine synthase truD family and contains one TRUD domain. The PUS7L gene is conserved in chimpanzee, canine, bovine, mouse, chicken and zebrafish, and maps to human chromosome 12q12. Encoding over 1,100 genes within 132 million bases, chromosome 12 makes up about 4.5 % of the human genome. A number of skeletal deformities are linked to chromosome 12 including hypochondrogenesis, achondrogenesis and Kniest dysplasia. Noonan syndrome, which includes heart and facial developmental defects among the primary symptoms, is caused by a mutant form of PTPN11 gene product, SH-PTP2. Chromosome 12 is also home to a homeobox gene cluster which encodes crucial transcription factors for morphogenesis, and the natural killer complex gene cluster encoding C-type lectin proteins which mediate the NK cell response to MHC I interaction.

    Gene Full Name: pseudouridine synthase 7 like

    基因ID

    83448

    UniProt

    Q9H0K6
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