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NAIP 抗体

NAIP 适用: 人 ELISA, IHC 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7239233
发货至: 中国
  • 抗原 See all NAIP 抗体
    NAIP (NLR Family, Apoptosis Inhibitory Protein (NAIP))
    适用
    • 31
    • 4
    • 2
    宿主
    • 31
    • 1
    • 1
    克隆类型
    • 31
    • 2
    多克隆
    标记
    • 16
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This NAIP antibody is un-conjugated
    应用范围
    • 27
    • 13
    • 13
    • 13
    • 7
    • 5
    • 4
    • 3
    • 3
    • 2
    • 1
    • 1
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    ELISA, Immunohistochemistry (IHC)
    产品特性
    Polyclonal Antibody
    纯化方法
    Affinity purification
    免疫原
    Synthetic peptide of human NAIP
    亚型
    IgG
    Top Product
    Discover our top product NAIP Primary Antibody
  • 应用备注
    IHC 1:25-1:100
    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    0.5 mg/mL
    缓冲液
    PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
    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
    Store at -20°C. Avoid freeze / thaw cycles.
  • 抗原
    NAIP (NLR Family, Apoptosis Inhibitory Protein (NAIP))
    别名
    NAIP (NAIP 产品)
    别名
    BIRC1 antibody, NLRB1 antibody, psiNAIP antibody, AV364616 antibody, Birc1a antibody, D13Lsd1 antibody, Naip antibody, Naip-rs1 antibody, NLR family apoptosis inhibitory protein antibody, NLR family, apoptosis inhibitory protein 1 antibody, NAIP antibody, Naip1 antibody
    背景
    This gene is part of a 500 kb inverted duplication on chromosome 5q13. This duplicated region contains at least four genes and repetitive elements which make it prone to rearrangements and deletions. The repetitiveness and complexity of the sequence have also caused difficulty in determining the organization of this genomic region. This copy of the gene is full length, additional copies with truncations and internal deletions are also present in this region of chromosome 5q13. It is thought that this gene is a modifier of spinal muscular atrophy caused by mutations in a neighboring gene, SMN1.
    NCBI登录号
    NP_004527
    UniProt
    Q13075
    途径
    Apoptosis, Inflammasome
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