Anti-Human /Mouse /Rat SEPT9 Polyclonal Antibody

SEPT9多克隆抗体

This gene is a member of the septin family involved in cytokinesis and cell cycle control. This gene is a candidate for the ovarian tumor suppressor gene. Mutations in this gene cause hereditary neuralgic amyotrophy, also known as neuritis with brachial predilection. A chromosomal translocation involving this gene on chromosome 17 and the MLL gene on chromosome 11 results in acute myelomonocytic leukemia. Multiple alternatively spliced transcript variants encoding different isoforms have been described.
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基本信息

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货号 PA03645
规格 100μl
宿主 Rabbit
免疫原 Recombinant protein of human SEPT9
特异性 Widely expressed. Isoforms are differentially expressed in testes, kidney, liver heart, spleen, brain, peripheral blood leukocytes, skeletal muscle and kidney. Specific isoforms appear to demonstrate tissue specificity. Isoform 5 is the most highly expressed in fetal tissue. Isoform 1 is detected in all tissues except the brain and thymus, while isoform 2, isoform 3, and isoform 4 are detected at low levels in approximately half of the fetal tissues.
亚型 IgG
反应性 Human ,Mouse ,Rat
克隆
Uniprot Q9UHD8
浓度 0.2 mg/mL
推荐稀释度 IHC 1:25-1:100
配方
应用范围 IHC,ELISA
别名 AF17q25,Cell division control protein septin D1,KIAA0991,MLL septin like fusion protein,MLL septin-like fusion protein,MLL septin-like fusion protein MSF-A,MSF,MSF1,NAPB,Ov/Br septin,Ovarian/breast septin alpha,Ovarian/Breast septin,PNUTL4,SEPT9,SEPT9,SeptD1,Septin 9,Septin D1,Septin-9,SINT1
保存条件 冻干产品: 2 - 8°C保存5年; 液体: -20°C保存2年.
注意 仅用于科学研究, 不能用于疾病诊断.

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