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Dipeptidyl-peptidase 1 (heavy chain, Cleaved-Leu231) Rabbit Polyclonal Antibody

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产品基本信息

产品货号
BD-PC0150
产品名称
Dipeptidyl-peptidase 1 (heavy chain, Cleaved-Leu231) Rabbit Polyclonal Antibody
别名
Dipeptidyl peptidase 1 (EC 3.4.14.1;Cathepsin C;Cathepsin J;Dipeptidyl peptidase I;DPP-I;DPPI;Dipeptidyl transferase) [Cleaved into: Dipeptidyl peptidase 1 exclusion domain chain (Dipeptidyl peptidase I exclusion domain chain); Dipeptidyl peptidase 1 heavy chain (Dipeptidyl peptidase I heavy chain); Dipeptidyl peptidase 1 light chain (Dipeptidyl peptidase I light chain)]
类别
常规抗体
基因名称
CTSC CPPI
蛋白名称
Dipeptidyl-peptidase 1 (heavy chain, Cleaved-Leu231)
推荐应用
WB
反应种属
Human,Rat,Mouse
浓度
1 mg/ml
存储缓冲液
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% New type preservative N.
Human Gene ID
1075
Human Gene Link
https://www.uniprot.org/uniprot/1075
Human Swissprot No.
P53634
Human Swissprot Link
https://www.uniprot.org/uniprotkb/P53634/entry
Mouse Gene ID
13032
Mouse Gene Link
https://www.uniprot.org/uniprot/13032
Mouse Swissprot No.
P97821
Mouse Swissprot Link
https://www.uniprot.org/uniprotkb/P97821
Rat Gene ID
25423
Rat Gene Link
https://www.uniprot.org/uniprot/25423
Rat Swissprot No.
P80067
Rat Swissprot Link
https://www.uniprot.org/uniprotkb/P80067
免疫原
Synthesized peptide derived from human Dipeptidyl-peptidase 1 (heavy chain, Cleaved-Leu231)
特异性
This antibody detects endogenous levels of Human Dipeptidyl-peptidase 2 (heavy chain, Cleaved-Leu231, protein was cleaved amino acid sequence between 230-231 )
稀释度
WB 1:1000-2000 ELISA 1:5000-20000
预测分子量
18kD
运输及保存条件
-20°C/1 year
宿主
Polyclonal, Rabbit,IgG
背景介绍
catalytic activity:Release of an N-terminal dipeptide, Xaa-Yaa-|-Zaa-, except when Xaa is Arg or Lys, or Yaa or Zaa is Pro.,cofactor:Binds 1 chloride ion per heavy chain.,disease:Defects in CTSC are a cause of Haim-Munk syndrome (HMS) [MIM:245010]; also known as keratosis palmoplantaris with periodontopathia and onychogryposis or Cochin Jewish disorder. HMS is an autosomal recessive disorder characterized by palmoplantar keratosis, onychogryphosis and periodontitis. Additional features are pes planus, arachnodactyly, and acroosteolysis.,disease:Defects in CTSC are a cause of juvenile periodontitis (JPD) [MIM:170650]; also known as prepubertal periodontitis (PPP). JPD is characterized by severe and protracted gingival infections, leading to tooth loss. JPD inheritance is autosomal dominant.,disease:Defects in CTSC are a cause of Papillon-Lefevre syndrome (PLS) [MIM:245000]; also known as keratosis palmoplantaris with periodontopathia. PLS is an autosomal recessive disorder characterized by palmoplantar keratosis and severe periodontitis affecting deciduous and permanent dentitions and resulting in premature tooth loss. The palmoplantar keratotic phenotype vary from mild psoriasiform scaly skin to overt hyperkeratosis. Keratosis also affects other sites such as elbows and knees.,enzyme regulation:Strongly inhibited by the cysteine peptidase inhibitors mersalyl acid, iodoacetic acid and cystatin. Inhibited by N-ethylmaleimide, Gly-Phe-diazomethane, TLCK, TPCK and, at low pH, by dithiodipyridine. Not inhibited by the serine peptidase inhibitor PMSF, the aminopeptidase inhibitor bestatin, or metal ion chelators.,function:Thiol protease. Has dipeptidylpeptidase activity. Active against a broad range of dipeptide substrates composed of both polar and hydrophobic amino acids. Proline cannot occupy the P1 position and arginine cannot occupy the P2 position of the substrate. Can act as both an exopeptidase and endopeptidase. Activates serine proteases such as elastase, cathepsin G and granzymes A and B. Can also activate neuraminidase and factor XIII.,induction:Up-regulated in lymphocytes by IL2.,online information:CTSC mutation db,PTM:In approximately 50% of the complexes the exclusion domain is cleaved at position 58 or 61. The two parts of the exclusion domain are held together by a disulfide bond.,PTM:N-glycosylated.,similarity:Belongs to the peptidase C1 family.,subunit:Tetramer of heterotrimers consisting of exclusion domain, heavy- and light chains.,tissue specificity:Ubiquitous. Highly expressed in lung, kidney and placenta. Detected at intermediate levels in colon, small intestine, spleen and pancreas.,
组织表达
Ubiquitous. Highly expressed in lung, kidney and placenta. Detected at intermediate levels in colon, small intestine, spleen and pancreas.
细胞定位
Lysosome.
功能
proteolysis,?immune response,?aging,?response to organic substance,
期货
现货
纯化
The antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen.

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