FITC标记的锌指蛋白673抗体
产品名称: FITC标记的锌指蛋白673抗体
英文名称: Anti-ZNF673/FITC
产品编号: HZ-16523R-FITC
产品价格: null
产品产地: 中国/上海
品牌商标: HZbscience
更新时间: 2023-08-17T10:24:20
使用范围: ICC=1:50-200 IF=1:50-200
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Rabbit Anti-ZNF673/FITC Conjugated antibody
FITC标记的锌指蛋白673抗体
英文名称 | Anti-ZNF673/FITC |
中文名称 | FITC标记的锌指蛋白673抗体 |
别 名 | Protein ZNF673; RP4-733D15.4; zinc finger family member 673; ZN673_HUMAN; ZNF673. |
规格价格 | 100ul/2980元 购买 大包装/询价 |
说 明 书 | 100ul |
研究领域 | 转录调节因子 锌指蛋白 表观遗传学 |
抗体来源 | Rabbit |
克隆类型 | Polyclonal |
交叉反应 | Human, |
产品应用 | ICC=1:50-200 IF=1:50-200 not yet tested in other applications. optimal dilutions/concentrations should be determined by the end user. |
分 子 量 | 20kDa |
性 状 | Lyophilized or Liquid |
浓 度 | 1mg/ml |
免 疫 原 | KLH conjugated synthetic peptide derived from human ZNF673 |
亚 型 | IgG |
纯化方法 | affinity purified by Protein A |
储 存 液 | 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol. |
保存条件 | Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20°C. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C. |
产品介绍 | background: This encodes a zinc finger protein with an N-terminal KRAB (Kruppel-associated) domain found in transcriptional repressors. This gene is located in a region of the X chromosome thought to be involved in nonsyndromic X-linked mental retardation. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2011] Tissue Specificity: Expressed in brain, ovary, testis, prostate, tonsil, heart, bone marrow, colon, breast and kidney. Similarity: Contains 1 KRAB domain. Database links: Entrez Gene: 55634 Human Omim: 300585 Human SwissProt: Q5JUW0 Human Unigene: 632800 Human Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications |
这编码锌指蛋白与N-末端KrAb(Krbpel-相关)结构域在转录阻遏物中发现。该基因位于X染色体的一个区域,被认为参与了非综合征性X连锁精神发育迟滞。该基因已发现编码不同亚型的多个转录变体。[ RefSeq,Aug 2011提供]