超碰97自拍_久久99久久98精品免观看软件_在线亚洲一区_九九视频这里只有精品_国产精品一区二区欧美视频_精品国产区一区

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
99久久国产综合精品五月天,国产亚洲在线观看,国产大BBWBBWHD视频
首頁 > 產品中心 > 一抗 > 產品信息
PLEKHG5 Rabbit pAb (bs-12455R)  
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-12455R
英文名稱 PLEKHG5 Rabbit pAb
中文名稱 凋亡誘導受體PLEKHG5抗體
別    名 PKHG5_HUMAN; Pleckstrin homology domain-containing family G member 5; PH domain-containing family G member 5; Guanine nucleotide exchange factor 720; GEF720.  
研究領域 染色質和核信號  信號轉導  G蛋白偶聯受體  G蛋白信號  
抗體來源 Rabbit
克隆類型 Polyclonal
克 隆 號
交叉反應 Mouse,Rat (predicted: Human,Rabbit,Pig,Cow,Dog,Horse)
產品應用 IHC-P=1:100-500,IHC-F=1:100-500,IF=1:100-500
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
理論分子量 116 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 PLEKHG5: 951-1062/1062 
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 This gene encodes a protein that activates the nuclear factor kappa B (NFKB1) signaling pathway. Mutations in this gene are associated with autosomal recessive distal spinal muscular atrophy. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2012]

Function:
Guanine nucleotide exchange factor that activates RHOA and maybe the NF-kappa-B signaling pathway. Involved in the control of neuronal cell differentiation. Plays a role in angiogenesis through regulation of endothelial cells chemotaxis.

Subunit:
Interacts with GIPC1/synectin and RHOA.

Subcellular Location:
Cytoplasm. Cytoplasm, perinuclear region. Cell junction. Cell projection, lamellipodium. Note=Predominantly cytoplasmic, however when cells are stimulated found in perinuclear regions. Localized at cell-cell junctions in quiescent endothelial cells, it relocalizes to cytoplasmic vesicle and the leading edge of lamellipodia in migrating endothelial cells.

Tissue Specificity:
Predominantly expressed in the peripheral nervous system and brain. Highest expression is observed in heart, lung, kidney, testis and moderate expression is present in spleen, pancreas, skeletal muscle, ovary and liver. Weakly expressed in glioblastoma (GBM) cell lines.

DISEASE:
Distal spinal muscular atrophy, autosomal recessive, 4 (DSMA4) [MIM:611067]: A neuromuscular disorder. Distal spinal muscular atrophy, also known as distal hereditary motor neuronopathy, represents a heterogeneous group of neuromuscular disorders caused by selective degeneration of motor neurons in the anterior horn of the spinal cord, without sensory deficit in the posterior horn. The overall clinical picture consists of a classical distal muscular atrophy syndrome in the legs without clinical sensory loss. The disease starts with weakness and wasting of distal muscles of the anterior tibial and peroneal compartments of the legs. Later on, weakness and atrophy may expand to the proximal muscles of the lower limbs and/or to the distal upper limbs. DSMA4 is characterized by childhood onset, generalized muscle weakness and atrophy with denervation and normal sensation. Bulbar symptoms and pyramidal signs are absent. Note=The disease is caused by mutations affecting the gene represented in this entry.
Charcot-Marie-Tooth disease, recessive, intermediate type, C (CMTRIC) [MIM:615376]: A form of Charcot-Marie-Tooth disease, a disorder of the peripheral nervous system, characterized by progressive weakness and atrophy, initially of the peroneal muscles and later of the distal muscles of the arms. Recessive intermediate forms of Charcot-Marie-Tooth disease are characterized by clinical and pathologic features intermediate between demyelinating and axonal peripheral neuropathies, and motor median nerve conduction velocities ranging from 25 to 45 m/sec. Note=The disease is caused by mutations affecting the gene represented in this entry.

Similarity:
Contains 1 DH (DBL-homology) domain.
Contains 1 PH domain.

SWISS:
O94827

Gene ID:
57449

Database links:

Entrez Gene: 57449 Human

Entrez Gene: 269608 Mouse

Entrez Gene: 310999 Rat

Omim: 611101 Human

SwissProt: O94827 Human

SwissProt: Q66T02 Mouse

SwissProt: Q6RFZ7 Rat

Unigene: 284232 Human

Unigene: 332102 Mouse

Unigene: 486442 Mouse

Unigene: 20730 Rat



產品圖片
Paraformaldehyde-fixed, paraffin embedded (Mouse brain); Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15min; Block endogenous peroxidase by 3% hydrogen peroxide for 20 minutes; Blocking buffer (normal goat serum) at 37°C for 30min; Antibody incubation with (PLEKHG5) Polyclonal Antibody, Unconjugated (bs-12455R) at 1:400 overnight at 4°C, followed by operating according to SP Kit(Rabbit) (sp-0023) instructionsand DAB staining.
Paraformaldehyde-fixed, paraffin embedded (Rat liver); Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15min; Block endogenous peroxidase by 3% hydrogen peroxide for 20 minutes; Blocking buffer (normal goat serum) at 37°C for 30min; Antibody incubation with (PLEKHG5) Polyclonal Antibody, Unconjugated (bs-12455R) at 1:400 overnight at 4°C, followed by operating according to SP Kit(Rabbit) (sp-0023) instructionsand DAB staining.
版權所有 2004-2026 www.ggggww.cn 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: 5566日本婷婷色中文字幕 | 国产亚洲欧美日韩夜色凹凸成人 | www.亚洲国产 | 狠狠躁夜夜躁人人爽超碰97香蕉 | 亚洲一区二区三区写真 | 国产午夜成人久久无码一区二区 | 伊人网综合视频 | 久久精品中文字幕有码 | 4438╳全国最大色倩网址 | 日韩亚洲制服丝袜中文字幕 | 99久久国语露脸精品国产 | 色香欲综合成人免费视频 | 福利视频一区二区三区 | 国产精品私密保健会所 | av在线网站免费观看 | 国产亚洲欧美日韩夜色凹凸成人 | 黄色成年人国语版在线观看 | 欧美亚洲另类激情另类 | 特级淫片女子高清视频在线观看 | 麻豆传媒免费视频 | 国产精品久久久aaa 欧美乱强伦XXXXX | 在线成人免费网站 | 国产视频福利 | 国产性猛交粗暴力xxxx | 亚洲伊人久久综合成人网站 | 日韩国产成人无码AV毛片 | 黄v在线观看 | 四虎永久在线精品免费A | 冲田杏梨一区二区三区 | 亚洲精品乱码久久久久久蜜桃91 | 99久久精品国产一区二区成人 | 国产精品十八禁一区二区三区 | 精品女同一区二区三区免费播放 | 亚洲视频中文字幕在线 | 97成人超碰视 | gay18无套网站| 视频国产一区二区 | 久久av麻豆| 麻豆综合在线 | 国产亚洲欧美精品一区 | 亚洲欧美国产成人 |