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NBPF3 抗体 (N-Term)

NBPF3 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN5517639
发货至: 中国
  • 抗原 See all NBPF3 抗体
    NBPF3 (Neuroblastoma Breakpoint Family, Member 3 (NBPF3))
    抗原表位
    • 5
    • 1
    • 1
    N-Term
    适用
    宿主
    • 13
    克隆类型
    • 13
    多克隆
    标记
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This NBPF3 antibody is un-conjugated
    应用范围
    • 5
    • 3
    • 1
    Western Blotting (WB)
    序列
    CDQVKKEDQE ATSPRLSREL LDEKEPEVLQ DSLDRFYSTP FEYLELPDLC
    预测反应
    Human: 100%
    产品特性
    This is a rabbit polyclonal antibody against NBPF3. It was validated on Western Blot.
    纯化方法
    Affinity Purified
    免疫原
    The immunogen is a synthetic peptide directed towards the N-terminal region of Human NBPF3
    Top Product
    Discover our top product NBPF3 Primary Antibody
  • 应用备注
    Optimal working dilution should be determined by the investigator.
    限制
    仅限研究用
  • 状态
    Liquid
    缓冲液
    Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.
    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
    For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
  • 抗原
    NBPF3 (Neuroblastoma Breakpoint Family, Member 3 (NBPF3))
    别名
    NBPF3 (NBPF3 产品)
    别名
    AE2 antibody, NBPF member 3 antibody, NBPF3 antibody
    背景
    This gene is a member of the neuroblastoma breakpoint family (NBPF) which consists of dozens of recently duplicated genes primarily located in segmental duplications on human chromosome 1. This gene family has experienced its greatest expansion within the human lineage and has expanded, to a lesser extent, among primates in general. Members of this gene family are characterized by tandemly repeated copies of DUF1220 protein domains. DUF1220 copy number variations in human chromosomal region 1q21.1, where most DUF1220 domains are located, have been implicated in a number of developmental and neurogenetic diseases such as microcephaly, macrocephaly, autism, schizophrenia, mental retardation, congenital heart disease, neuroblastoma, and congenital kidney and urinary tract anomalies. Altered expression of some gene family members is associated with several types of cancer. This gene family contains numerous pseudogenes.

    Alias Symbols: NBPF3, L7,

    Protein Interaction Partner: NBPF3, APP, UBD, UBC, TSEN15, ANK1, EWSR1,

    Protein Size: 275
    基因ID
    84224
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