麻豆av资源_日本三级一区_www.狠狠艹_国产精妇在线观看第一区_成人性生交大片免费看中国A片_日本一本久久

掃碼關注公眾號           掃碼咨詢技術支持           掃碼咨詢技術服務
  
客服熱線:400-901-9800  客服QQ:4009019800  技術答疑  技術支持  質量反饋  關于我們  聯系我們
肥美欧美内射中出,人人爽人人爽人人爽人人片av ,国产成人一级毛片
首頁 > 產品中心 > 一抗 > 產品信息
DDHD1 Rabbit pAb (bs-14221R)  
訂購熱線:400-901-9800
訂購郵箱:sales@bioss.com.cn
訂購QQ:  400-901-9800
技術支持:techsupport@bioss.com.cn
50ul/1180.00元
100ul/1980.00元
200ul/2800.00元
大包裝/詢價
產品編號 bs-14221R
英文名稱 DDHD1 Rabbit pAb
中文名稱 磷脂酶DDHD1抗體
別    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 recessive); SPG28.  
研究領域 細胞生物  信號轉導  新陳代謝  
抗體來源 Rabbit
克隆類型 Polyclonal
克 隆 號
交叉反應 (predicted: Human,Mouse,Rat,Rabbit,Pig,Sheep,Cow,Dog)
產品應用 IHC-P=1:100-500,IHC-F=1:100-500,IF=1:100-500,ICC/IF=1:100-500,ELISA=1:5000-10000
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
理論分子量 100 kDa
檢測分子量
細胞定位 細胞漿 
性    狀 Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human DDHD1: 751-850/900 
亞    型 IgG
純化方法 affinity purified by Protein A
緩 沖 液 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
保存條件 Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
注意事項 This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed PubMed
產品介紹 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, 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.

Similarity:
Belongs to the PA-PLA1 family.
Contains 1 DDHD domain.

SWISS:
Q8NEL9

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



版權所有 2004-2026 m.jywcc.com 北京博奧森生物技術有限公司
通過國際質量管理體系ISO 9001:2015 GB/T 19001-2016    證書編號: 00124Q34771R2M/1100
通過國際醫療器械-質量管理體系ISO 13485:2016 GB/T 42061-2022    證書編號: CQC24QY10047R0M/1100
京ICP備05066980號-1         京公網安備110107000727號
主站蜘蛛池模板: 亚洲第一在线综合网站 | 亚洲精品午夜国产va久久成人 | 一级毛片视频免费看 | 亚洲超高清大胆极品人体美女 | 四虎成人精品无码永久在线 | 亚洲а∨天堂久久精品喷水 | 高清国产在线观看 | 中文字幕在线播 | 91亚洲福利 | 91日韩免费 | h网站在线播放 | 一二三四视频在线观看中文版免费 | 182tv人之初午夜精品视频 | 91大神在线看 | 亚洲日本乱码一区二区在线二产线 | 爽爽淫人网 | 久久精品视频一区二区三区 | 亚洲一区二区三区自拍公司 | 91夫妻在线 | 凯蒂夫人在线播放 | 欧美日韩大片在线观看 | 啊啊啊国产视频 | 国产人人爱| 精品国产一区二区三区观看不卡 | 中文字幕AV无码免费一区 | 五月av综合av国产av | 亚洲av日韩av无码黑人 | 3344成人免费看A片 | 午夜影视啪啪免费体验区入口 | 天堂成人国产精品一区 | 亚洲日韩乱码中文无码蜜桃臀 | 热久久视久久精品2019 | 国产精品啪一品二区三区粉嫩 | 中文字幕在线观看日 | 在线观看麻豆传媒 | 亚洲av无码成h人动漫在线观看3d | 伊人第四色 | 日本韩国国产 | av免费福利 | 日韩不卡视频在线观看 | 亚洲第一天堂影院 |