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HGD 抗体 (Middle Region)

This anti-HGD antibody is a 兔 多克隆 antibody detecting HGD in WB. Suitable for 人, 小鼠, 大鼠, 斑马鱼, Cow, 犬, 豚鼠, 马 和 兔.
产品编号 ABIN2784538
发货至: 中国

Quick Overview for HGD 抗体 (Middle Region) (ABIN2784538)

抗原

See all HGD 抗体
HGD (Homogentisate 1,2-Dioxygenase (HGD))

适用

人, 小鼠, 大鼠, 斑马鱼, Cow, 犬, 豚鼠, 马, 兔

宿主

  • 52
  • 6

克隆类型

  • 51
  • 7
多克隆

标记

  • 29
  • 7
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This HGD antibody is un-conjugated

应用范围

  • 44
  • 22
  • 16
  • 13
  • 13
  • 13
  • 9
  • 6
  • 3
  • 3
  • 2
  • 1
  • 1
Western Blotting (WB)
  • 抗原表位

    • 15
    • 5
    • 5
    • 4
    • 4
    • 2
    • 2
    • 2
    • 1
    • 1
    Middle Region

    序列

    KLFAAKQDVS PFNVVAWHGN YTPYKYNLKN FMVINSVAFD HADPSIFTVL

    预测反应

    Cow: 93%, Dog: 93%, Guinea Pig: 93%, Horse: 93%, Human: 100%, Mouse: 93%, Rabbit: 93%, Rat: 93%, Zebrafish: 86%

    产品特性

    This is a rabbit polyclonal antibody against HGD. It was validated on Western Blot using a cell lysate as a positive control.

    纯化方法

    Affinity Purified

    免疫原

    The immunogen is a synthetic peptide directed towards the middle region of human HGD
  • 应用备注

    Optimal working dilutions should be determined experimentally by the investigator.

    说明

    Antigen size: 445 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

    HGD (Homogentisate 1,2-Dioxygenase (HGD))

    别名

    HGD

    背景

    Homogentisate 1,2-dioxygenase (HGD) gene mutations are the molecular cause of alkaptonuria, a rare hereditary disorder of the phenylalanine catabolism. The highest expression of HGD is in the prostate, small intestine, colon, and liver. The HGD gene contains 14 exons. Conflicting reports have placed the gene at 3q2, 3q13.3-q21, 3q21-q24, 3q21-q23, or 3q25-q26.Homogentisate 1,2-dioxygenase (HGD) gene mutations are the molecular cause of alkaptonuria, a rare hereditary disorder of the phenylalanine catabolism. The highest expression of HGD is in the prostate, small intestine, colon, and liver. The HGD gene contains 14 exons. Conflicting reports have placed the gene at 3q2, 3q13.3-q21, 3q21-q24, 3q21-q23, or 3q25-q26. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.
    Alias Symbols: AKU, HGO
    Protein Interaction Partner: HGD, Dlg4, GIT2, PCDHGC3, CLDN7, TERF1, CTBP2, CTBP1,
    Protein Size: 445

    分子量

    50 kDa

    基因ID

    3081

    NCBI登录号

    NM_000187, NP_000178

    UniProt

    Q93099
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