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锌指转录蛋白Sall4抗体

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产品名称: 锌指转录蛋白Sall4抗体
产品型号: SALL4
产品展商: 单克隆抗体/多克隆抗体
产品文档: 无相关文档

简单介绍

锌指转录蛋白Sall4抗体应用于IHC、WB、 IF、IP、ELISA等科研实验,按理化性质和生物学功能IgM、IgG、IgA、IgE、IgD五类。按抗体的来源,可将其分为天然抗体和**抗体。锌指转录蛋白Sall4抗体生产每个流程都执行严格的检测标准,保证蛋白抗原产品质量,质量稳定,实验效果明显。


锌指转录蛋白Sall4抗体  的详细介绍

锌指转录蛋白Sall4抗

规格:1mg/1ml

英文名: SALL4

别名: AA407717; ZNF797; AL022809; AW536104; C330011P20Rik; C78083; C78563; Sal like 4 (Drosophila); Sal like 4; Sal like Protein 4; Sal-like protein 4; Sall4; SALL4_HUMAN; Tex20; Zinc finger protein 797; Zi

分子量: 112kDa

储存液:0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glyce

克隆类型:Polyclonal

亚型:IgG

纯化方法:affinity purified by Protein A

**原:KLH conjugated synthetic peptide derived from human SALL4 (5

交叉反应:Human, Mouse, Rat, Chicken, Dog, Pig, Cow, Horse, Sheep,

细胞定位:细胞核

锌指转录蛋白Sall4抗产品介绍:background: Sall4 is mammalian homologs of the Drosophila region-specific homeotic gene spalt, which encodes a zinc finger-containing transcription regulator. Drosophila spalt is an essential genetic component required for the specification of posterior head and anterior tail as opposed to trunk. Sall3 is expressed at 24 weeks of gestation in several regions of the human fetal brain including neurons of the hippocampus formation and of mediodorsal and ventrolateral thalamic nuclei, Purkinje cells of the cerebellum, and a subset of neurons in the brainstem. Sall4 expression in early mouse embryos is gradually confined to the head region and the primitive streak, followed by prominent expression in the developing midbrain, branchial arches, limbs and genital papilla. Function: Probable transcription factor. Subcellular Location: Nucleus. 锌指转录蛋白Sall4抗Tissue Specificity: Expressed in testis. DISEASE: Defects in SALL4 are the cause of Duane-radial ray syndrome (DRRS) [MIM:607323]; also known as Okihiro syndrome. DRRS is a disorder characterized by the association of forearm malformations with Duane retraction syndrome. Defects in SALL4 are the cause of oculootoradial syndrome (OORS) [MIM:147750]. Oculootoradial syndrome is an autosomal dominant condition characterized by upper limbs anomalies (radial ray defects, carpal bones fusion), extraocular motor disturbances, congenital bilateral non-progressive mixed hearing loss. Other less consistent malformations include heart involvement, mild thrombocytopenia and leukocytosis (before age 50),锌指转录蛋白Sall4抗shoulder girdle hypoplasia, imperforate anus, kidney malrotation or rectovaginal fistula. The IVIC syndrome is an allelic disorder of Duane-radial ray syndrome (DRRS) with a similar phenotype. Similarity: Belongs to the sal C2H2-type zinc-finger protein family. Contains 7 C2H2-type zinc fingers. Gene ID: 57167 Database links: Entrez Gene: 57167 Human Entrez Gene: 99377 Mouse Omim: 607343 Human SwissProt: Q9UJQ4 Human SwissProt: Q8BX22 Mouse Unigene: 517113 Human Unigene: 434054 Mouse Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

锌指转录蛋白Sall4抗产品应用:WB=1:100-500 ELISA=1:500-1000 IHC-P=1:100-500 IHC-F=1:100-500 ICC=1:100-500 IF=1:100-500 (石蜡切片需做抗原修复) not yet tested in other applications. optimal dilutions/concentrations should be determined by the end user.

研究领域:细胞生物  发育生物学  信号转导  干细胞  转录调节因子  锌指蛋白  表观遗传学  

储存条件: Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.

来源: Rabbit

外观: Lyophilized or Liquid


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