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Retinoid X Receptor alpha 抗体

This anti-Retinoid X Receptor alpha antibody is a 兔 多克隆 antibody detecting Retinoid X Receptor alpha in WB, IHC (p) 和 IF (p). Suitable for 人, 小鼠 和 大鼠.
产品编号 ABIN685702
发货至: 中国

Quick Overview for Retinoid X Receptor alpha 抗体 (ABIN685702)

抗原

See all Retinoid X Receptor alpha (RXRA) 抗体
Retinoid X Receptor alpha (RXRA) (Retinoid X Receptor, alpha (RXRA))

适用

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人, 小鼠, 大鼠

宿主

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克隆类型

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多克隆

标记

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This Retinoid X Receptor alpha antibody is un-conjugated

应用范围

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Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
  • 交叉反应

    人, 小鼠, 大鼠

    纯化方法

    Purified by Protein A.

    免疫原

    KLH conjugated synthetic peptide derived from human RXR Alpha

    亚型

    IgG
  • 应用备注

    WB(1:100-1000), IHC-P(1:100-500), IF(IHC-P)(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 1 % BSA, 50 % glycerol and 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

    -20 °C

    储存方法

    Store at -20°C for 12 months.

    有效期

    12 months
  • 抗原

    Retinoid X Receptor alpha (RXRA) (Retinoid X Receptor, alpha (RXRA))

    背景

    Synonyms: Retinoid X receptor alpha, FLJ16020, FLJ16733, MGC102720, NR2B1, Retinoic acid receptor RXR alpha, RXR alpha1, RXRalpha1, retinoid-X receptor alpha.

    Background: The WNT gene family consists of structurally related genes which encode secreted signaling proteins. These proteins have been implicated in oncogenesis and in several developmental processes, including regulation of cell fate and patterning during embryogenesis. This gene is a member of the WNT gene family. It is very conserved in evolution, and the protein encoded by this gene is known to be 98 % identical to the mouse Wnt1 protein at the amino acid level. The studies in mouse indicate that the Wnt1 protein functions in the induction of the mesencephalon and cerebellum. This gene was originally considered as a candidate gene for Joubert syndrome, an autosomal recessive disorder with cerebellar hypoplasia as a leading feature. However, further studies suggested that the gene mutations might not have a significant role in Joubert syndrome. This gene is clustered with another family member, WNT10B, in the chromosome 12q13 region.

    基因ID

    6256

    途径

    Nuclear Receptor Transcription Pathway, Retinoic Acid Receptor Signaling Pathway, Steroid Hormone Mediated Signaling Pathway, Regulation of Lipid Metabolism by PPARalpha, Hepatitis C
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