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DTNA 抗体 (C-Term)

This anti-DTNA antibody is a 兔 多克隆 antibody detecting DTNA in WB. Suitable for 人, 小鼠, 大鼠, 犬, 马, Cow, 豚鼠 和 Saccharomyces cerevisiae.
产品编号 ABIN2788807
发货至: 中国

Quick Overview for DTNA 抗体 (C-Term) (ABIN2788807)

抗原

See all DTNA 抗体
DTNA (Dystrobrevin alpha (DTNA))

适用

人, 小鼠, 大鼠, 犬, 马, Cow, 豚鼠, Saccharomyces cerevisiae

宿主

  • 15
  • 7

克隆类型

  • 18
  • 4
多克隆

标记

  • 17
  • 1
  • 1
  • 1
  • 1
  • 1
This DTNA antibody is un-conjugated

应用范围

  • 21
  • 14
  • 9
  • 8
  • 5
  • 3
  • 3
  • 1
  • 1
Western Blotting (WB)
  • 抗原表位

    • 8
    • 4
    • 2
    • 2
    • 1
    • 1
    • 1
    C-Term

    序列

    GATTSTMRGD MVTEDADPYV QPEDENYEND SVRQLENELQ MEEYLKQKLQ

    预测反应

    Cow: 92%, Dog: 100%, Guinea Pig: 93%, Horse: 100%, Human: 100%, Mouse: 86%, Rat: 92%, Yeast: 83%

    产品特性

    This is a rabbit polyclonal antibody against DTNA. It was validated on Western Blot.

    纯化方法

    Affinity Purified
  • 应用备注

    Optimal working dilutions should be determined experimentally by the investigator.

    说明

    Antigen size: 452 AA

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    Lot specific

    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.

    注意事项

    Avoid repeated freeze-thaw cycles.

    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

    DTNA (Dystrobrevin alpha (DTNA))

    别名

    DTNA

    背景

    The protein encoded by this gene belongs to the dystrobrevin subfamily of the dystrophin family. This protein is a component of the dystrophin-associated protein complex (DPC), which consists of dystrophin and several integral and peripheral membrane proteins, including dystroglycans, sarcoglycans, syntrophins and alpha- and beta-dystrobrevin. The DPC localizes to the sarcolemma and its disruption is associated with various forms of muscular dystrophy. Mutations in this gene are associated with left ventricular noncompaction with congenital heart defects. Multiple alternatively spliced transcript variants encoding different isoforms have been identified for this gene.
    Alias Symbols: D18S892E, DRP3, DTN, FLJ96209, LVNC1
    Protein Interaction Partner: SNTA1, ADRA1D, TJP1, ACTB, MLC1, NUP62, SEC23A, SEC24C, PSEN1, MYO1E, GFI1B, MARK2, SYNC, SNTG2, SNTG1, KCNJ12, SYNM, DTNBP1, SNTB2, SNTB1, DMD, DRP2, UTRN, ACTA1,
    Protein Size: 452

    分子量

    49 kDa

    基因ID

    1837

    NCBI登录号

    NM_001198942, NP_001185871

    UniProt

    B4DIR0
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