Rabbit Anti-TJP2/FITC Conjugated antibody
|别 名||Friedreich ataxia region gene X104 (tight junction protein ZO-2); MGC26306; Tight junction protein 2; Tight junction protein ZO 2; Tight junction protein ZO-2; TJP2; X104; ZO 2; ZO-2; ZO2; ZO2_HUMAN; Zona occludens protein 2; Zonula occludens protein 2|
|规格价格||100ul/2980元 购买 大包装/询价|
|说 明 书||100ul|
|交叉反应||Human, Mouse, Rat, Chicken, Dog, Cow, Horse, Rabbit, Sheep, Guinea Pig, Danio rerio|
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
|分 子 量||131kDa|
|性 状||Lyophilized or Liquid|
|免 疫 原||KLH conjugated synthetic peptide derived from human TJP2|
|纯化方法||affinity purified by Protein A|
|储 存 液||0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.|
|保存条件||Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20°C. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C.|
This gene encodes a zonula occluden that is a member of the membrane-associated guanylate kinase homolog family. The encoded protein functions as a component of the tight junction barrier in epithelial and endothelial cells and is necessary for proper assembly of tight junctions. Mutations in this gene have been identified in patients with hypercholanemia, and genomic duplication of a 270 kb region including this gene causes autosomal dominant deafness-51. Alternatively spliced transcripts encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Nov 2011].
Plays a role in tight junctions and adherens junctions
Homodimer, and heterodimer with ZO1. Interacts with occludin, SAFB and UBN1. Interaction with SAFB occurs in the nucleus. Interacts with SCRIB.
Cell junction, adherens junction. Cell membrane; Peripheral membrane protein; Cytoplasmic side. Cell junction, tight junction. Nucleus. Note=Also nuclear under environmental stress conditions and in migratory endothelial cells and subconfluent epithelial cell cultures.
This protein is found in epithelial cell junctions. Isoform A1 is abundant in the heart and brain. Detected in brain and skeletal muscle. It is present almost exclusively in normal tissues. Isoform C1 is expressed at high level in the kidney, pancreas, heart and placenta. Not detected in brain and skeletal muscle. Found in normal as well as in most neoplastic tissues.
Defects in TJP2 are involved in familial hypercholanemia (FHCA) [MIM:607748]. FHCA is a disorder characterized by elevated serum bile acid concentrations, itching, and fat malabsorption.
Belongs to the MAGUK family.
Contains 1 guanylate kinase-like domain.
Contains 3 PDZ (DHR) domains.
Contains 1 SH3 domain.
Entrez Gene: 9414 Human
Entrez Gene: 21873 Mouse
Entrez Gene: 115769 Rat
Omim: 607709 Human
SwissProt: Q9UDY2 Human
SwissProt: Q9Z0U1 Mouse
Unigene: 50382 Human
Unigene: 104744 Mouse
Unigene: 10965 Rat
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications
该基因编码一个膜小带，它是膜相关鸟苷酸激酶同系物家族的成员。编码蛋白是上皮细胞和内皮细胞紧密连接屏障的组成部分，是紧密连接正确组装所必需的。该基因的突变已经在高胆碱血症患者中鉴定出来，包括该基因在内的270kb区域的基因组重复导致常染色体显性聋-51。另一种编码多个异构体的剪接转录本已被观察到该基因。[ RefSeq，NOV 2011 ]提供。