Anti-HOXA11/FITC Conjugated抗体-抗体-抗体-生物在线

Anti-HOXA11/FITC Conjugated抗体

商家询价

产品名称： Anti-HOXA11/FITC Conjugated抗体

英文名称： Anti-HOXA11/FITC

产品编号： YB--6666R-FITC

产品价格： null

产品产地：中国/美国

品牌商标： Ybscience

更新时间： 2023-08-17T10:29:50

使用范围：科研使用

上海钰博生物科技有限公司

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所在区域 : 上海
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产品详情

Anti-HOXA11/FITC Conjugated抗体

产品编号	YB-6666R-FITC
英文名称	Anti-HOXA11/FITC
中文名称	FITC标记的同源盒蛋白HOXA11抗体
别名	HXA11_HUMAN; Hox 1I; Homeo box 1I; Homeo box A11; Homeobox A11; Homeobox protein Hox-A11; Homeobox protein HOXA11; Hox-1I; HOX1; HOX1I.
规格价格	100ul/2980元购买大包装/询价
说明书	100ul
研究领域	细胞生物信号转导转录调节因子表观遗传学
抗体来源	Rabbit
克隆类型	Polyclonal
交叉反应	Human, Mouse, Rat, Dog, Cow, Horse, Rabbit,
产品应用	IF=1:50-200 not yet tested in other applications. optimal dilutions/concentrations should be determined by the end user.
分子量	34kDa
性状	Lyophilized or Liquid
浓度	1mg/ml
免疫原	KLH conjugated synthetic peptide derived from human HOXA11
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: In vertebrates, the genes encoding the class of transcription factors called homeobox genes are found in clusters named A, B, C, and D on four separate chromosomes. Expression of these proteins is spatially and temporally regulated during embryonic development. This gene is part of the A cluster on chromosome 7 and encodes a DNA-binding transcription factor which may regulate gene expression, morphogenesis, and differentiation. This gene is involved in the regulation of uterine development and is required for female fertility. Mutations in this gene can cause radio-ulnar synostosis with amegakaryocytic thrombocytopenia. Function: Sequence-specific transcription factor which is part of a developmental regulatory system that provides cells with specific positional identities on the anterior-posterior axis. Subcellular Location: Nuclear DISEASE: Defects in HOXA11 are the cause of radioulnar synostosis with amegakaryocytic thrombocytopenia (RSAT) [MIM:605432]. The syndrome consists of an unusual association of bone marrow failure and skeletal defects. Patients have the same skeletal defects, the proximal fusion of the radius and ulna, resulting in extremely limited pronation and supination of the forearm. Some patients have also symptomatic thrombocytopenia, with bruising and bleeding problems since birth, necessitating correction by bone marrow or umbilical-cord stem-cell transplantation. Similarity: Belongs to the Abd-B homeobox family. Contains 1 homeobox DNA-binding domain. Database links: Entrez Gene: 3207 Human Entrez Gene: 15396 Mouse Omim: 142958 Human SwissProt: P31270 Human SwissProt: P31311 Mouse SwissProt: Q3V026 Mouse Unigene: 249171 Human Unigene: 26954 Mouse Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.