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C16orf57 抗体 (N-Term)

USB1 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN5517969
发货至: 中国
  • 抗原 See all C16orf57 (USB1) 抗体
    C16orf57 (USB1) (U6 SnRNA Biogenesis 1 (USB1))
    抗原表位
    • 4
    • 2
    • 1
    • 1
    • 1
    • 1
    N-Term
    适用
    • 25
    • 18
    • 18
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    宿主
    • 22
    • 2
    • 1
    克隆类型
    • 25
    多克隆
    标记
    • 8
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This C16orf57 antibody is un-conjugated
    应用范围
    • 21
    • 13
    • 4
    • 3
    • 1
    Western Blotting (WB)
    序列
    LVGYSSSGSE DESEDGMRTR PGDGSHRRGQ SPLPRQRFPV PDSVLNMFPG
    纯化方法
    Affinity purified
    免疫原
    The immunogen is a synthetic peptide directed towards the N terminal region of human C16ORF57
    Top Product
    Discover our top product USB1 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
    C16orf57 (USB1) (U6 SnRNA Biogenesis 1 (USB1))
    别名
    C16ORF57 (USB1 产品)
    别名
    C16orf57 antibody, HVSL1 antibody, Mpn1 antibody, PN antibody, hUsb1 antibody, C18H16orf57 antibody, AA960436 antibody, RGD1305215 antibody, c16orf57 antibody, C2H16orf57 antibody, zgc:91896 antibody, U6 snRNA biogenesis phosphodiesterase 1 antibody, U6 snRNA biogenesis 1 antibody, U6 snRNA biogenesis phosphodiesterase 1 L homeolog antibody, USB1 antibody, Usb1 antibody, usb1.L antibody, usb1 antibody
    背景
    This gene encodes a protein with several conserved domains, however, its exact function is not known. Mutations in this gene are associated with poikiloderma with neutropenia (PN), which shows phenotypic overlap with Rothmund-Thomson syndrome (RTS) caused by mutations in the RECQL4 gene. It is believed that this gene product interacts with RECQL4 protein via SMAD4 proteins, explaining the partial clinical overlap between PN and RTS. Alternatively spliced transcript variants encoding different isoforms have been noted for this gene.

    Alias Symbols: PN, Mpn1, HVSL1, hUsb1, C16orf57

    Protein Size: 186
    基因ID
    79650
    NCBI登录号
    NM_001195302, NP_001182231
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