电话:
400-7060-959
传真:
+86 10 56315212-8813
电子邮件:
orders@antibodies-online.cn

TRIM37 抗体 (AA 850-900)

TRIM37 适用: 人 IP 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7452461
发货至: 中国
  • 抗原 See all TRIM37 抗体
    TRIM37 (Tripartite Motif Containing 37 (TRIM37))
    抗原表位
    • 10
    • 8
    • 6
    • 5
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 850-900
    适用
    • 30
    • 3
    • 3
    • 3
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    宿主
    • 28
    • 1
    • 1
    克隆类型
    • 29
    • 1
    多克隆
    标记
    • 16
    • 4
    • 3
    • 3
    • 2
    • 2
    This TRIM37 antibody is un-conjugated
    应用范围
    • 23
    • 19
    • 3
    • 3
    • 2
    • 1
    Immunoprecipitation (IP)
    原理
    Rabbit anti-TRIM37 Antibody, Affinity Purified
    纯化方法
    Affinity Purified
    免疫原
    between AA 850 and 900
    亚型
    IgG
    Top Product
    Discover our top product TRIM37 Primary Antibody
  • 应用备注

    IP: 2 - 5 μg/mg lysate

    WB: Not recommended. Use rabbit anti-TRIM37 antibody ABIN7452119.

    限制
    仅限研究用
  • 浓度
    1000 μg/mL
    缓冲液
    Tris-citrate/phosphate buffer, pH 7 to 8 containing 0.09 % 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
    4 °C
    有效期
    12 months
  • 抗原
    TRIM37 (Tripartite Motif Containing 37 (TRIM37))
    别名
    TRIM37 (TRIM37 产品)
    别名
    MUL antibody, POB1 antibody, TEF3 antibody, 1110032A10Rik antibody, 2810004E07Rik antibody, AI848587 antibody, AU043018 antibody, mKIAA0898 antibody, tripartite motif-containing 37 antibody, tripartite motif containing 37 antibody, Trim37 antibody, TRIM37 antibody
    背景
    Background: TRIM37 is a member of the tripartite motif RBCC/Trim domain family that contains a RING-finger domain, B-boxes, and an alpha-helical coiled-coil region. TRIM37 is a peroxisomal protein whose function has not been determined. Mutations in TRIM37 result in mulibrey (MUscle, LIver, BRain, and EYes) nanism ('dwarfism'), a rare autosomal recessive disorder characterized by defects in tissues of mesodermal origin.
    基因ID
    4591
    NCBI登录号
    NP_056109
    UniProt
    O94972
You are here: