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LRRC59 抗体 (AA 20-307) (APC)

This 兔 多克隆 antibody specifically detects LRRC59 in FACS. It exhibits reactivity toward 人, 小鼠 和 大鼠.
产品编号 ABIN8005541
发货至: 中国
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Quick Overview for LRRC59 抗体 (AA 20-307) (APC) (ABIN8005541)

抗原

See all LRRC59 抗体
LRRC59 (Leucine Rich Repeat Containing 59 (LRRC59))

适用

  • 23
  • 21
  • 19
  • 4
  • 3
  • 3
  • 3
  • 3
  • 2
  • 1
  • 1
人, 小鼠, 大鼠

宿主

  • 24

克隆类型

  • 24
多克隆

标记

  • 15
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This LRRC59 antibody is conjugated to APC

应用范围

  • 17
  • 10
  • 9
  • 6
  • 6
  • 4
  • 3
  • 1
  • 1
  • 1
  • 1
Flow Cytometry (FACS)
  • 抗原表位

    • 12
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 20-307

    原理

    Anti-LRRC59 Antibody APC 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 LRRC59 recombinant protein (Position: L20-Q307).

    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

    LRRC59 (Leucine Rich Repeat Containing 59 (LRRC59))

    别名

    LRRC59

    背景

    Background: Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8 % of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes Lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma.

    Gene Full Name: leucine rich repeat containing 59

    基因ID

    55379

    UniProt

    Q96AG4
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