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LRRC47 抗体 (AA 309-583)

The 兔 多克隆 anti-LRRC47 antibody is suitable to detect LRRC47 in samples from 人. It has been validated for WB, ELISA 和 FACS.
产品编号 ABIN7601245
发货至: 中国
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Quick Overview for LRRC47 抗体 (AA 309-583) (ABIN7601245)

抗原

LRRC47 (Leucine Rich Repeat Containing 47 (LRRC47))

适用

  • 4
  • 3
  • 1

宿主

  • 4

克隆类型

  • 4
多克隆

标记

  • 4
This LRRC47 antibody is un-conjugated

应用范围

  • 4
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB), ELISA, Flow Cytometry (FACS)
  • 抗原表位

    • 1
    • 1
    • 1
    AA 309-583

    原理

    Anti-LRRC47 Antibody

    交叉反应 (详细)

    No cross reactivity with other proteins.

    产品特性

    Anti-LRRC47 Antibody. Tested in ELISA, WB, Flow Cytometry applications. This antibody reacts with Human.

    纯化方法

    Immunogen affinity purified.

    免疫原

    E.coli-derived human LRRC47 recombinant protein (Position: L309-R583).

    亚型

    IgG
  • 应用备注

    Western blot, 0.1-0.25 μg/mL, Human Flow Cytometry (Fixed), 1-3 μg/1x106 cells, Human ELISA, 0.1-0.5 μg/mL, -

    限制

    仅限研究用
  • 状态

    Lyophilized

    溶解方式

    Adding 0.2 mL of distilled water will yield a concentration of 500 μg/mL.

    浓度

    500 μg/mL

    缓冲液

    Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4.

    储存条件

    4 °C,-20 °C

    储存方法

    At -20°C for one year from date of receipt. After reconstitution, at 4°C for one month.
    It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freezing and thawing.

    有效期

    12 months
  • 抗原

    LRRC47 (Leucine Rich Repeat Containing 47 (LRRC47))

    别名

    LRRC47

    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 47

    分子量

    68 kDa

    基因ID

    57470

    UniProt

    Q8N1G4
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