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LMAN1 抗体

This anti-LMAN1 antibody is a 小鼠 单克隆 antibody detecting LMAN1 in WB, IHC, IF 和 FACS. Suitable for 人 和 犬.
产品编号 ABIN2724842
发货至: 中国

Quick Overview for LMAN1 抗体 (ABIN2724842)

抗原

See all LMAN1 抗体
LMAN1 (Lectin, Mannose-Binding, 1 (LMAN1))

适用

  • 45
  • 15
  • 13
  • 6
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
人, 犬

宿主

  • 43
  • 2
小鼠

克隆类型

  • 37
  • 8
单克隆

标记

  • 27
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This LMAN1 antibody is un-conjugated

应用范围

  • 40
  • 15
  • 15
  • 14
  • 13
  • 13
  • 10
  • 5
  • 3
  • 3
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF), Flow Cytometry (FACS)

克隆位点

1E3
  • 产品特性

    Homo sapiens lectin, mannose-binding, 1 (LMAN1)

    纯化方法

    Purified from mouse ascites fluids by affinity chromatography

    免疫原

    Full length human recombinant protein of human LMAN1 (NP_005561) produced in HEK293T cell.

    亚型

    IgG1
  • 应用备注

    WB 1:500~2000, IHC 1:150, IF 1:100, FLOW 1:100

    说明

    The concentration of the product may vary between diferrent lots.

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    0.5-1.0 mg/mL

    缓冲液

    PBS (PH 7.3) containing 1 % BSA, 50 % glycerol and 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
  • 抗原

    LMAN1 (Lectin, Mannose-Binding, 1 (LMAN1))

    别名

    LMAN1

    背景

    The protein encoded by this gene is a type I integral membrane protein localized in the intermediate region between the endoplasmic reticulum and the Golgi, presumably recycling between the two compartments. The protein is a mannose-specific lectin and is a member of a novel family of plant lectin homologs in the secretory pathway of animal cells. Mutations in the gene are associated with a coagulation defect. Using positional cloning, the gene was identified as the disease gene leading to combined factor V-factor VIII deficiency, a rare, autosomal recessive disorder in which both coagulation factors V and VIII are diminished.

    分子量

    54.2 kDa

    基因ID

    3998

    NCBI登录号

    NM_005570

    HGNC

    3998
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