Anti-KLKB1 Antibody (CAB5318)
- SKU:
- CAB5318
- Product type:
- Antibody
- Reactivity:
- Human
- Reactivity:
- Mouse
- Reactivity:
- Rat
- Host Species:
- Rabbit
- Isotype:
- IgG
- Antibody Type:
- Polyclonal Antibody
- Research Area:
- Cardiovascular
Frequently bought together:
Description
抗体名: | Anti-KLKB1 Antibody |
抗体コード: | CAB5318 |
抗体サイズ: | 20uL, 50uL, 100uL |
申し込み: | WB IHC |
反応性: | Human, Mouse, Rat |
宿主種: | Rabbit |
免疫原: | Recombinant fusion protein containing a sequence corresponding to amino acids 20-300 of human KLKB1 (NP_000883.2). |
申し込み: | WB IHC |
推奨希釈: | WB 1:500 - 1:2000 IHC 1:50 - 1:200 |
反応性: | Human, Mouse, Rat |
ポジティブサンプル: | HepG2, HT-29, 293T, BxPC-3, Mouse liver, Rat liver |
免疫原: | Recombinant fusion protein containing a sequence corresponding to amino acids 20-300 of human KLKB1 (NP_000883.2). |
精製方法: | Affinity purification |
ストレージバッファ: | Store at -20'C. Avoid freeze / thaw cycles. Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3. |
アイソタイプ: | IgG |
順序: | GCLT QLYE NAFF RGGD VASM YTPN AQYC QMRC TFHP RCLL FSFL PASS INDM EKRF GCFL KDSV TGTL PKVH RTGA VSGH SLKQ CGHQ ISAC HRDI YKGV DMRG VNFN VSKV SSVE ECQK RCTS NIRC QFFS YATQ TFHK AEYR NNCL LKYS PGGT PTAI KVLS NVES GFSL KPCA LSEI GCHM NIFQ HLAF SDVD VARV LTPD AFVC RTIC TYHP NCLF FTFY TNVW KIES QRNV CLLK TSES GTPS SSTP QENT ISGY SLLT CKRT LPEP CHSK IYPG V |
遺伝子ID: | 3818 |
Uniprot: | P03952 |
セルラーロケーション: | Secreted |
計算された分子量: | 71kDa |
観察された分子量: | 71kDa |
同義語: | KLKB1, KLK3, PKK, PKKD, PPK |
バックグラウンド: | This gene encodes a glycoprotein that participates in the surface-dependent activation of blood coagulation, fibrinolysis, kinin generation and inflammation. The encoded preproprotein present in plasma as a non-covalent complex with high molecular weight kininogen undergoes proteolytic processing mediated by activated coagulation factor XII to generate a disulfide-linked, heterodimeric serine protease comprised of heavy and light chains. Certain mutations in this gene cause prekallikrein deficiency. Alternative splicing results in multiple transcript variants encoding different isoforms. |
UniProt Protein Function: | KLKB1: The enzyme cleaves Lys-Arg and Arg-Ser bonds. It activates, in a reciprocal reaction, factor XII after its binding to a negatively charged surface. It also releases bradykinin from HMW kininogen and may also play a role in the renin-angiotensin system by converting prorenin into renin. Defects in KLKB1 are the cause of prekallikrein deficiency (PKK deficiency); also known as Fletcher factor deficiency. This disorder is a blood coagulation defect. Belongs to the peptidase S1 family. Plasma kallikrein subfamily. |
UniProt Protein Details: | Protein type:Secreted; EC 3.4.21.34; Protease; Secreted, signal peptide Chromosomal Location of Human Ortholog: 4q35 Cellular Component: extracellular space; plasma membrane; extracellular region Molecular Function:protein binding; serine-type endopeptidase activity Biological Process: extracellular matrix disassembly; extracellular matrix organization and biogenesis; fibrinolysis; positive regulation of fibrinolysis; zymogen activation; proteolysis; blood coagulation; blood coagulation, intrinsic pathway; Factor XII activation; plasminogen activation Disease: Prekallikrein Deficiency |
NCBI Summary: | Plasma prekallikrein is a glycoprotein that participates in the surface-dependent activation of blood coagulation, fibrinolysis, kinin generation and inflammation. It is synthesized in the liver and secreted into the blood as a single polypeptide chain. Plasma prekallikrein is converted to plasma kallikrein by factor XIIa by the cleavage of an internal Arg-Ile bond. Plasma kallikrein therefore is composed of a heavy chain and a light chain held together by a disulphide bond. The heavy chain originates from the amino-terminal end of the zymogen and contains 4 tandem repeats of 90 or 91 amino acids. Each repeat harbors a novel structure called the apple domain. The heavy chain is required for the surface-dependent pro-coagulant activity of plasma kallikrein. The light chain contains the active site or catalytic domain of the enzyme and is homologous to the trypsin family of serine proteases. Plasma prekallikrein deficiency causes a prolonged activated partial thromboplastin time in patients. [provided by RefSeq, Jul 2008] |
UniProt Code: | P03952 |
NCBI GenInfo Identifier: | 125184 |
NCBI Gene ID: | 3818 |
NCBI Accession: | P03952.1 |
UniProt Secondary Accession: | P03952,Q17RE8, Q17RE9, Q4W5C3, A6NH96, B2R8H9, |
UniProt Related Accession: | P03952 |
Molecular Weight: | 71,370 Da |
NCBI Full Name: | Plasma kallikrein |
NCBI Synonym Full Names: | kallikrein B, plasma (Fletcher factor) 1 |
NCBI Official Symbol: | KLKB1 |
NCBI Official Synonym Symbols: | PPK; KLK3 |
NCBI Protein Information: | plasma kallikrein; kininogenin; Fletcher factor; plasma prekallikrein; plasma kallikrein heavy chain; plasma kallikrein light chain |
UniProt Protein Name: | Plasma kallikrein |
UniProt Synonym Protein Names: | Fletcher factor; Kininogenin; Plasma prekallikrein |
Protein Family: | Protein kinase |
UniProt Gene Name: | KLKB1 |
UniProt Entry Name: | KLKB1_HUMAN |
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