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磷脂酶DDHD1抗体

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产品名称: 磷脂酶DDHD1抗体
产品型号: DDHD1
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

磷脂酶DDHD1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。磷脂酶DDHD1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。


磷脂酶DDHD1抗体  的详细介绍

磷脂酶DDHD1抗体

规格:1mg/1ml

英文名: DDHD1

别名: DDHD domain containing 1; DDHD domain containing protein 1; KIAA1705; PA-PLA1; PAPLA1; Phosphatidic acid-preferring phospholipase A1 homolog; Phospholipase DDHD1; Spastic paraplegia 28 (autosomal rece

分子量: 100kDa

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 DDHD1

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

细胞定位:细胞浆

磷脂酶DDHD1抗体产品介绍:background: Phosphatidic acid is released following cell activation and functions as a second messenger in several signaling pathways. DDHD1 is a lipase that catalyzes degradation of phosphatidic acid and attenuates cell activation. Function: Phospholipase that hydrolyzes phosphatidic acid, including 1,2-dioleoyl-sn-phosphatidic acid. The different isoforms may change the substrate specificity. Subunit: Forms homooligomers and, to a much smaller extent, heterooligomers with DDHD2. Subcellular Location: Cytoplasmic Tissue Specificity: Highly expressed in testis. Also expressed in brain, spleen and lung. Only expressed in cerebellum in fetal brain. DISEASE: Spastic paraplegia 28, autosomal recessive (SPG28) [MIM:609340]: A form of spastic paraplegia, a neurodegenerative disorder characterized by a slow, gradual,磷脂酶DDHD1抗体 progressive weakness and spasticity of the lower limbs. Rate of progression and the severity of symptoms are quite variable. Initial symptoms may include difficulty with balance, weakness and stiffness in the legs, muscle spasms, and dragging the toes when walking. In some forms of the disorder, bladder symptoms (such as incontinence) may appear, or the weakness and stiffness may spread to other parts of the body. Some SPG28 patients also have distal sensory impairment. Note=The disease is caused by mutations affecting the gene represented in this entry磷脂酶DDHD1抗体. Similarity: Belongs to the PA-PLA1 family. Contains 1 DDHD domain. Gene ID: 80821 Database links: Entrez Gene: 80821 Human Entrez Gene: 114874 Mouse Entrez Gene: 305816 Rat Omim: 614603 Human SwissProt: Q8NEL9 Human SwissProt: Q80YA3 Mouse Unigene: 125525 Human Unigene: 121918 Mouse Unigene: 163271 Rat Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

磷脂酶DDHD1抗体产品应用: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  信号转导  新陈代谢  

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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