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HMX2 抗体 (AA 122-200) (FITC)

This anti-HMX2 antibody is a 兔 多克隆 antibody detecting HMX2 in IF (cc) 和 IF (p). Suitable for 人.
产品编号 ABIN1393712
发货至: 中国

Quick Overview for HMX2 抗体 (AA 122-200) (FITC) (ABIN1393712)

抗原

See all HMX2 抗体
HMX2 (H6 Family Homeobox 2 (HMX2))

适用

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宿主

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克隆类型

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多克隆

标记

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This HMX2 antibody is conjugated to FITC

应用范围

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Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
  • 抗原表位

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    AA 122-200

    预测反应

    Human,Mouse,Dog,Cow,Pig,Horse,Chicken,Rabbit

    纯化方法

    Purified by Protein A.

    免疫原

    KLH conjugated synthetic peptide derived from human HMX2

    亚型

    IgG
  • 应用备注

    IF(IHC-P) 1:50-200
    IF(IHC-F) 1:50-200
    IF(ICC) 1:50-200

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1 μg/μL

    缓冲液

    Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

    储存液

    ProClin

    注意事项

    This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

    储存条件

    -20 °C

    储存方法

    Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

    有效期

    12 months
  • 抗原

    HMX2 (H6 Family Homeobox 2 (HMX2))

    别名

    HMX2

    背景

    Synonyms: H6 family homeo box 2, H6 family homeobox 2, H6 homeo box 2, H6L, HMX 2, HMX2 , HMX2_HUMAN , Homeo box H6 family 2, Homeo box protein H6 family member 2, Homeobox H6 family 2 , Homeobox protein H6 family member 2, Homeobox protein HMX2, Nkx5 2.

    Background: The homeobox DNA-binding domain is a 60 amino acid motif that is conserved among many species and functions to bind DNA via a helix-turn-helix structure, thereby playing a role in transcriptional regulation and the control of gene expression. HMX2 (H6 family homeobox 2), also known as H6L or Nkx5-2, is a 273 amino acid nuclear protein that belongs to the HMX homeobox family and contains one homeobox DNA-binding domain. HMX2 functions as a transcription factor that assists in specification of neuronal cell types and is essential for proper development of hypothalamus and inner ear. Hemizygous deletions of the gene encoding HMX2 are thought to lead to vestibular dysfunction, inner ear malformations and congenital sensorineural hearing loss.

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