58
23
3
6
Cat. No. | Product Name | Form | Specificity Of Inhibition |
---|---|---|---|
C0045 |
RIPA Lysis Buffer (Strong)
RIPA裂解液(强) |
Solution in bottle | |
C0046 |
RIPA Lysis Buffer (Medium)
RIPA裂解液(中) |
Solution in bottle | |
C0047 |
RIPA Lysis Buffer (Weak)
RIPA裂解液(弱) |
Solution in bottle |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T35788 |
Orlistat Degradation Product (sodium salt)
|
Others | Others |
Orlistat degradation product is a degradation product of the digestive lipase inhibitor orlistat . It is formed via hydrolytic and thermal degradation as well as digestion by human carboxyl ester lipase. | |||
T20933 |
Bis(p-chlorophenyl)acetic acid
Bis(p-chlorphenyl)essigsaeure,Bis(4-chlorophenyl)acetic acid,DDA (degradation product),DDA |
Others | Others |
Bis(p-chlorophenyl)acetic acid is a standard for pesticide residue analysis. | |||
T39598 |
4-Chlorocatechol
|
Others | Others |
4-Chlorocatechol, a significant degradation product of 4-chloro-2-aminophenol (4C2AP), serves as a substrate for both catechol 1,2-dioxygenases and chlorocatechol dioxygenase [1] [2]. | |||
T21572 |
Erythromycin A enol ether
|
Others | Others |
Erythromycin A enol ether 是大环内酯类抗生素红霉素A 的降解产物。 | |||
T7440 |
p,p'-DDE
p,p'-dichlorodiphenyldichloroethylene,4,4'-DDE,Dichlorodiphenyldichloroethylene,2,2-双(4-氯苯基)-1,1-二氯乙烯 |
Androgen Receptor; Drug Metabolite | Endocrinology/Hormones; Metabolism |
p,p'-DDE (p,p'-dichlorodiphenyldichloroethylene) 是持久性 DDT 的主要代谢物。4,4'-DDE 是一种有效的雄激素受体拮抗剂,IC50=5 μM,Ki=3.5 μM。 | |||
T38961L |
DP-1 hydrochloride
DP-1 hydrochloride(1472616-61-7 Free base) |
Drug Metabolite | Metabolism |
DP-1 hydrochloride是 SDC-TRAP-0063 的降解产物,是 Ganetespib 的一个片段。Ganetespib 是一种具有抗肿瘤活性的热休克蛋白 90 (HSP90) 抑制剂。 | |||
T38003 |
Levofloxacin N-oxide
|
Others | Others |
Levofloxacin N-oxide 是从左氧氟沙星中分离出来的杂质。 | |||
T0983L |
DL-Penicillamine
3-Sulfanylvaline,DL-青霉胺 |
Antibiotic | Microbiology/Virology |
DL-Penicillamine (3-Sulfanylvaline) 是一种螯合剂,推荐用于去除威尔逊病患者体内多余的铜。 它仅存在于使用或服用该药物的个体中。它是青霉素类抗生素最具特征的降解产物。它被用作抗风湿药和威尔逊病的螯合剂。 | |||
T34439 |
Rubreserine
|
Others | Others |
degradation product | |||
T32527 |
Lactenocin
Demycarosylmacrocin |
Others | Others |
Lactenocin is a active degradation product. | |||
T19545 |
Raloxifene N-Oxide
|
Others | Others |
Raloxifene N-Oxide is a Raloxifene oxidative degradation product. | |||
T33879 |
Papaveraldine
Xanthaline |
Others | Others |
Papaveraldine is a benzylisoquinoline alkaloid that papaverine degradation product. | |||
T71226 |
Opc 15161
|
Others | Others |
Opc 15161 is a degradation product of OPC-15160 and superoxide inhibitor. | |||
T39339 |
Ochratoxin α
|
Others | Others |
Ochratoxin α is a less toxic photolytic and thermal degradation product of Ochratoxin A. | |||
T19785 |
Isocyclosporin A
IsocyclosporinA,Isocyclosporin-A |
Others | Others |
Isocyclosporin A is a rearranged degradation product. It is formed by acid treatment of cyclosporin A under aqueous and non-aqueous conditions. | |||
T84986 |
Descarbonyl Lacosamide
DP-I |
Others | Others |
Descarbonyl-lacosamide is a potential impurity in commercial lacosamide preparations. It is a degradation product that forms under acidic conditions. | |||
T38177 |
Flambalactone
|
Others | Others |
Flambalactone is a degradation product formed by methanolysis of the antibiotic flambamycin. | |||
T35882 |
Rizatriptan N-oxide
|
Others | Others |
Rizatriptan N-oxide is a potential impurity found in commercial preparations of rizatriptan.1It is a degradation product formed under oxidative conditions. | |||
T11000 |
Descarbamoyl cefuroxime
|
Others | Others |
Descarbamoyl cefuroxime is also an intermediate in the synthesis of cephalosporin antibiotics. Decarbamyl cefuroxime is a degradation product of cefuroxime. | |||
T36721 |
Dehydro Amlodipine (fumarate)
|
Others | Others |
Dehydro amlodipine is a potential impurity found in commercial preparations of amlodipine. It is a degradation product formed during storage or when amlodipine is subjected to oxidative or acidic conditions or undergoes photo or electrochemical degradation. | |||
T19380 |
Iretol
|
Others | Others |
Iretol (2,4,6-trihydroxyanisole), serving as an intermediate in the synthesis of natural isoflavones including Tectorigenin, Irigenin, and Caviunin, is identified as a degradation product of a glucoside derived from Iris Jorentina. | |||
T37915 |
Monodes(N-carboxymethyl)valine Daclatasvir
|
Others | Others |
Monodes(N-carboxymethyl)valine Daclatasvir, also known as Daclatasvir Impurity A, is the principal degradation product of Daclatasvir.Daclatasvir is a potent inhibitor of the HCV NS5A protein[1]. | |||
T37704 |
Olanzapine Lactam Impurity
|
Others | Others |
Olanzapine lactam impurity is a potential impurity found in commercial preparations of olanzapine.1It is a degradation product formed by exposure to thermal or oxidative stress. 1.Baertschi, S.W., Brunner, H., Bunnell, C.A., et al.Isolation, identification, and synthesis of two oxidative degradation products of olanzapine (LY170053) in solid oral formulationsJ. Pharm. Sci.97(2)883-892(2008) | |||
T68890 |
Desvaleryl Valsartan
|
Others | Others |
Desvaleryl valsartan is a potential impurity found in commercial preparations of the angiotensin II type 1 (AT1) receptor antagonist valsartan. It is a degradation product formed under acidic conditions. | |||
T35734 |
Doramectin monosaccharide
|
Others | Others |
Doramectin monosaccharide is an acid degradation product of doramectin , a disaccharide-containing anthelmintic that potentiates glutamate- and GABA-gated chloride channel opening in nematodes. Doramectin undergoes acid-catalyzed hydrolysis to form doramectin monosaccharide. | |||
T36751 |
Dihydroxy Melphalan
|
Others | Others |
Dihydroxy melphalan is an inactive degradation product of melphalan . It is formed by the hydrolysis of melphalan via the intermediate monohydroxy melphalan in aqueous solutions, including cell culture medium and human plasma. | |||
T36599 |
4-Epianhydrotetracycline hydrochloride
|
Others | Others |
Epianhydrotetracycline (EATC) is a degradation product of the antibiotic tetracycline .1 EATC is active against Pseudomonas, Agrobacterium, Moraxella, Bacillus, and E. coli (MIC50s = 0.75-16 mg/L). | |||
T84933 |
Meclizine N-oxide
Meclozine N-oxide |
Others | Others |
Meclizine N-oxide, a metabolite of the histamine H1 receptor antagonist meclizine (1), also acts as a degradation product and potential impurity in commercial meclizine preparations (2). | |||
T84628 |
Safinamide Acid
|
Others | Others |
Safinamide acid, a potential impurity in commercial safinamide preparations and a degradation product of safinamide under thermal and oxidative stress, is encountered in the pharmaceutical formulation process. | |||
T36030 |
Desethylene Ciprofloxacin (hydrochloride)
|
Others | Others |
Desethylene ciprofloxacin is a major metabolite of ciprofloxacin . It is also a degradation product of ciprofloxacin that can be created through advanced oxygenation processes as a potential way to remove ciprofloxacin from wastewater. It is also created during degradation of ciprofloxacin by chlorination. | |||
T37380 |
Pseudoerythromycin A enol ether
|
Others | Others |
Pseudoerythromycin A enol ether is a degradation product of erythromycin. It does not possess antibiotic activity and can be used as an analytical standard for erythromycin A stability studies. | |||
TP1598 |
Tyroserleutide hydrochloride
|
||
Tyroserleutide hydrochloride is a small molecule tripeptide isolated from the degradation product of pig spleen, which can inhibit tumor growth in vivo and in vitro. | |||
T38337 |
Isochlortetracycline
|
Others | Others |
Isochlortetracycline 是广谱抗生素金霉素降解的无活性碱性产物。 | |||
T84927 |
Lansoprazole N-oxide
|
Others | Others |
Lansoprazole N-oxide is a potential impurity in lansoprazole bulk preparations, identified as a degradation product under acidic or basic conditions. This compound is related to lansoprazole, a proton pump inhibitor. | |||
T38961 |
DP-1
|
Others | Others |
DP-1, a Ganetespib degradation product, represents a fragment derived from SDC-TRAP-0063. Ganetespib itself functions as an inhibitor of heat shock protein 90 (HSP90), exhibiting notable anti-tumor properties. | |||
T35733 |
Doramectin aglycone
|
Others | Others |
Doramectin aglycone is an acid degradation product of doramectin , a disaccharide-containing anthelmintic that potentiates glutamate- and GABA-gated chloride channel opening in nematodes, and its acid-catalyzed hydrolysis product doramectin monosaccharide . Doramectin undergoes one round of acid-catalyzed hydrolysis to form doramectin monosaccharide which is then hydrolyzed again to remove the remaining saccharide unit and form doramectin aglycone. | |||
T76587 |
(Asp28)-Exenatide
|
||
(Asp28)-Exenatide 是艾塞那肽 的降解产物。(Asp28)-Exenatide 可用作GLP-1R 激动剂。 | |||
T73723 |
Bifenazate-diazene
|
Others | Others |
Bifenazate-diazene 是 Bifenazate 的主要降解产物。Bifenazate 是一种选择性杀螨剂和杀虫剂。 | |||
T38379 |
4-tert-Octylphenol diethoxylate
|
Others | Others |
4-tert-Octylphenol diethoxylate is a degradation product of the multi-purpose surfactant, Triton X. A known environmental contaminant, 4-tert-octylphenol diethoxylate is reported to be an endocrine disruptor in animal and human research studies, producing weak estrogenic effects. | |||
T84962 |
(3R,5R)-Rosuvastatin calcium
|
Others | Others |
(3R,5R)-Rosuvastatin, a potential impurity detected in bulk rosuvastatin formulations, arises as a degradation product through various stresses including acid or base hydrolysis, thermal, photolytic, hydrolytic, oxidative stress, or during storage. This compound is associated with the HMG-CoA reductase inhibitor class to which rosuvastatin belongs. | |||
T74078 |
N-Nitrosoglyphosate sodium
|
Others | Others |
N-Nitrosoglyphosate sodium 是亚硝胺的降解产物,是草甘膦除草剂的合成杂质。 | |||
T37246 |
Palonosetron N-oxide
|
Others | Others |
Palonosetron N-oxide is a metabolite of the serotonin (5-HT) receptor subtype 5-HT3antagonist palonosetron .1It is also a potential impurity in palonosetron preparations.2Palonosetron N-oxide is a degradation product formed by exposure to oxidative stress. 1.Stoltz, R.A., Cyong, J.-C., Shah, A., et al.Pharmacokinetic and safety evaluation of palonosetron, a 5-hydroxytryptamine-3 receptor antagonist, in U.S. and Japanese healthy subjectsJ. Clin. Pharmacol.44(5)520-531(2004) 2.Vishnu Murthy, M., S... | |||
T85127 |
Monohydroxy Melphalan hydrochloride
Hydroxymelphalan |
Others | Others |
Monohydroxy melphalan, a degradation product and DNA alkylating agent derived from melphalan, results from melphalan hydrolysis in aqueous solutions such as cell culture medium and human plasma. It enhances DNA adducts in ML-1 myeloblastic leukemia cells based on concentration and induces cytotoxicity with an IC50 value of 28.1 μg/ml. | |||
T85208 |
4-epi Minocycline
4-EMC,Minocycline Impurity A |
Others | Others |
4-epiMinocycline, recognized as a primary degradation product and a probable impurity in minocycline commercial formulations, is derived from minocycline, a broad-spectrum tetracycline antibiotic notable for its extended serum half-life. Besides treating acne, especially in older patients, minocylvania exhibits significant anti-inflammatory and neuroprotective effects. | |||
T36708 |
Monohydroxy Melphalan (hydrochloride)
|
Others | Others |
Monohydroxy melphalan is a DNA alkylating agent and a degradation product of melphalan . Monohydroxy melphalan is formed by the hydrolysis of melphalan in aqueous solutions, including cell culture medium and human plasma. It increases the level of DNA adducts in ML-1 myeloblastic leukemia cells in a concentration-dependent manner and induces cytotoxicity with an IC50 value of 28.1 μg/ml. | |||
T85303 |
(E)-2-Hexadecenal Alkyne
Click TagTM (E)-2-Hexadecenal Alkyne |
Others | Others |
"(E)-2-Hexadecenal alkyne is a click chemistry probe derivative of the sphingolipid degradation product (E)-2-hexadecenal. This compound has demonstrated the ability to induce cytoskeletal reorganization, leading to cell rounding, detachment, activation of downstream JNK targets, and apoptosis in various cell types. Furthermore, it readily reacts with deoxyguanosine and DNA, forming aldehyde-derived DNA adducts." | |||
T35458 |
(R)-nitro-Blebbistatin
|
Others | Others |
(R)-nitro-Blebbistatin is a more stable form of (+)-blebbistatin , which is the inactive form of (-)-blebbistatin . Prolonged exposure to blue light (450-490 nm) results in degradation of blebbistatin to an inactive product via cytotoxic intermediates, which may be problematic for its use in fluorescent live cell imaging applications. The addition of a nitro group stabilizes the molecule to circumvent its degradation by prolonged blue light exposure. (R)-nitro-Blebbistatin has the same stereoche... | |||
T74109 |
Captopril EP Impurity B
|
Others | Others |
CaptoprilEPImpurity B 是一种 Captopril 的杂质。Captopril 是一种含巯基的口服活性血管紧张素转换酶(ACE)抑制剂 (IC50=0.025 μM)。 | |||
T35929 |
O-Demethyl Apremilast
|
Others | Others |
O-Demethyl apremilast is an active metabolite of the phosphodiesterase 4 (PDE4) inhibitor apremilast .1It inhibits the activity of PDE4 isolated from U937 cells and LPS-induced TNF-α production in isolated human peripheral blood mononuclear cells (PBMCs; IC50s = 8.3 and 5.6 μM, respectively). O-Demethyl apremilast is also an oxidative degradation product of apremilast.2,3 1.Hoffmann, M., Kumar, G., Schafer, P., et al.Disposition, metabolism and mass balance of [14C]apremilast following oral admi... | |||
T36182 |
Neamine tetrahydrochloride
|
Others | Others |
Neamine tetrahydrochloride 是一种广谱氨基糖苷类抗生素,一种新霉素的降解产物。Neamine tetrahydrochloride 可通过靶向血管生成素 (angiogenin) 发挥抗血管生成作用。Neamine tetrahydrochloride 具有抗菌,抗肿瘤和神经保护活性。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T4940 |
3-Methylhistamine dihydrochloride
|
Others; Endogenous Metabolite | Metabolism; Others |
3-Methylhistamine dihydrochloride 是一种组胺的降解产物,与免疫反应有关,并在接种过疫苗的小鼠中表现出上调作用。 | |||
T4456 |
N4-Acetylcytidine
N4-乙酰胞苷,N-Acetylcytidine |
Others; Endogenous Metabolite | Metabolism; Others |
N4-Acetylcytidine (N-Acetylcytidine) 是内源性代谢产物的一种。 | |||
TN1833 |
Karacoline
|
NF-κB | NF-κB |
Karacoline 是发现于植物Aconitum kusnezoffii 中的一种二萜生物碱,通过 NF-κB 信号通路,抑制椎间盘退变中细胞外基质的降解。 | |||
T8244 |
Raspberry ketone glucoside
覆盆子酮葡糖苷,树莓苷,覆盆子酮葡萄糖甙 |
Others | Others |
Raspberry ketone glucoside 是一种山莓果实中的天然产物。它能够抑制黑色素的合成。 | |||
TN1892 |
Lusianthridin
|
Others; c-Myc | Cell Cycle/Checkpoint; Others |
Lusianthridin 是来自石斛 Dendrobium venustum 的天然产物。 Lusianthridin 在无毒浓度下表现出抗迁移特性。 Lusianthridin 通过抑制 Src-STAT3 信号传导增强 c-Myc 降解。 | |||
T2723 |
Ketoisophorone
茶香酮,4-Oxoisophorone,2,6,6-Trimethyl-2-cyclohexene-1,4-dione |
Others | Others |
Ketoisophorone (2,6,6-Trimethyl-2-cyclohexene-1,4-dione) 是工业上重要的环状内酯,是合成类胡萝卜素和调味剂的关键中间体。 | |||
T4887 |
3-Amino-2-methylpropanoic acid
DL-3-AMINOISOBUTYRIC ACID,3-氨基异丁酸,α-Methyl-β-alanine |
Endogenous Metabolite | Metabolism |
3-Amino-2-methylpropanoic acid (α-Methyl-β-alanine) 是 N-carbamyl-beta-aminoisobutyric acid 经 enzyme Beta-ureidopropionase (EC 3.5.1.6)转化后的产物,是嘧啶降解的最后一步。-尿嘧啶丙酸酶缺乏症是一种与神经异常相关的嘧啶降解的先天性错误。 | |||
T0983 |
Penicillamine
青霉胺,d-penicillamin,Dimethyl Cysteine,D-青霉胺,Artamine,D-(-)-Penicillamine |
Antibiotic | Microbiology/Virology |
Penicillamine (Artamine) 是一种 penicillin 的代谢降解产物,是一种螯合剂,可作用于威尔逊氏病。 | |||
T19124 |
3-Oxocholic acid
3-Ketocholic acid |
Endogenous Metabolite | Metabolism |
3-Oxocholic acid(3-Ketocholic acid) 是胆汁酸的代谢产物,也是产气荚膜梭菌在肠道中由胆汁降解的主要产物。33-Oxocholic acid 是一种主要存在于哺乳动物的胆汁中类固醇酸。 | |||
T5248 |
(R)-3-Hydroxybutanoic acid
|
Others; Endogenous Metabolite | Metabolism; Others |
(R)-3-Hydroxybutanoic acid 是一种代谢物,在 3-羟基丁酸脱氢酶催化下由乙酸乙酯转化而成。它可以作为营养来源和抗生素、维生素和信息素的前体。 | |||
T5060 |
2-Oxobutanoic acid
2-酮丁酸,alpha-Ketobutyric Acid,2-Oxobutyric acid,Propionylformic acid |
Others; Endogenous Metabolite | Metabolism; Others |
2-Oxobutanoic acid (alpha-Ketobutyric Acid) 是一种胱硫醚的酶促裂解产物。它也是苏氨酸的降解产物之一。 它能够转化为丙酰辅酶A,从而进入柠檬酸循环。 | |||
TN1637 |
Eurycomalactone
|
Anti-infection; NF-κB | Microbiology/Virology; NF-κB |
Eurycomalactone 是一种NF-κB 抑制剂,IC50=0.5 μM,是一种天然产物。它可抑制蛋白合成,降低 cyclin D1 蛋白水平,但对 TNFα 诱导的 IκBα 降解或 IKKα/β 和 IκBα 的磷酸化水平没有作用。 | |||
T6599 |
N6-methyladenosine
N6-甲基腺苷,N-Methyladenosine,6-Methyladenosine,NSC-29409,m6A |
Others; Influenza Virus; Endogenous Metabolite | Metabolism; Microbiology/Virology; Others |
N6-Methyladenosine 是甲基化的腺嘌呤残基,苷是转移核糖核酸降解的内源性尿核苷产物。它是存在于所有高等真核生物中最普遍的的信使 RNA 内部修饰,可修饰病毒 RNA,有抗病毒活性。 | |||
T5236 |
N-Methylhydantoin
甲酰乙内脲,Dioxy-creatinine,1-Methyl-hydantoin |
Others; Endogenous Metabolite | Metabolism; Others |
N-Methylhydantoin (1-Methyl-hydantoin) 是一种小分子量极性物质,是细菌降解肌酐的产物。在哺乳动物中,N-Methylhydantoin 的代谢是通过 5-hydroxy-1-methylhydantoin 进行的。在一个报告的人类病例中,N-Methylhydantoin 被发现是影响智力的物质dupracetam的代谢物。 | |||
T0665 |
Xanthine
2,6-Dihydroxypurine,海生丁(黄嘌呤),黄嘌呤,Isoxanthine |
Endogenous Metabolite; Adenosine Receptor | GPCR/G Protein; Metabolism; Neuroscience |
Xanthine (Isoxanthine) 是一种植物生物碱,存在于茶、咖啡和可可中。Xanthine 是温和的中枢神经系统激活剂,也是嘌呤降解途径的中间产物。 | |||
TCS2070 |
Homogentisic acid
高龙胆酸,2,5-dihydroxyphenylacetic acid,Homogentisinic Acid,Melanic acid |
Antioxidant; Endogenous Metabolite | Metabolism; oxidation-reduction |
Homogentisic acid (2,5-dihydroxyphenylacetic acid) 是一种尿液和血清代谢物中的特定代谢物,可用于尿黑酸尿症的诊断。 | |||
T10619 |
Bromelain
|
Apoptosis; Others | Apoptosis; Others |
Bromelain 是来源于菠萝茎的一种抗炎药,可诱导细胞凋亡,具有纤维蛋白溶解、抗癌、抗水肿和抗血栓形成活性。它通过下调血浆激肽原,抑制前列腺素 E2 表达,降解晚期糖基化终产物受体,在COX 途径上游发生抗氧化作用以及调节血管生成生物标志物而发挥作用。 | |||
T4716 |
Pyrrole-2-carboxylic acid
吡咯-2-羧酸,2-Pyrrolecarboxylic acid,Minaline |
Endogenous Metabolite | Metabolism |
Pyrrole-2-carboxylic acid (Minaline) 是一种天然生物碱类,从海洋细菌Pelomonas puraquaesp. Nov 中分离得到。 | |||
T4799 |
Indole
|
Others; Endogenous Metabolite | Metabolism; Others |
Indole 它具有双环结构,由一个六元苯环和一个五元含氮吡咯环融合而成。它可以由细菌作为氨基酸色氨酸的降解产物产生。它自然存在于人类粪便中,有强烈的粪便气味。然而,在非常低的浓度下,它有一种花香,是许多花香(如橙花)和香水的成分。 | |||
T5089 |
5-Aminovaleric acid
|
Others; Endogenous Metabolite | Metabolism; Others |
5-Aminovaleric acid 被认为是 GABA 的亚甲基同系物,是GABA 的弱激动剂。它是赖氨酸降解产物。 它既能够内源性产生,也能够通过赖氨酸的细菌分解代谢产生。 | |||
T40347 |
Eicosapentaenoic acid methyl ester
|
Others | Others |
Eicosapentaenoic acid methyl ester is a degradation product derived from monogalactosyl diacylglycerol, which is an apoptosis-inducing anticancer compound. | |||
T35743 |
Ivermectin B1a aglycone
|
Others | Others |
Ivermectin B1a aglycone is an acid degradation product produced by hydrolysis of the disaccharide unit of ivermectin. It can inhibit nematode larval development, but does not cause paralytic activity. | |||
TN7549 |
2-epi-Abamectin
epi-Avermectin B1a |
Others | Others |
2-epi-Abamectin, a degradation product of abamectin, exhibits toxicity towards the two-spotted spider mite in contact assays, possessing an LC50 value of 4 ppm. This indicates it is approximately 100-fold less potent than its precursor, abamectin. |
Cat. No. | Product Name | Species | Expression System |
---|---|---|---|
TMPK-00507 |
TREM2 Protein, Cynomolgus, Recombinant (His)
TREM2,Trem2a,PLOSL2,TREM-2,Trem2c,Trem2b |
Cynomolgus | HEK293 Cells |
TREM-2 (Triggering Receptor Expressed on Myeloid cells-2) is a 35 kDa type I transmembrane member of the TREM family and Ig superfamily. Mature human TREM-2 consists of a 156 amino acid (aa) extracellular domain (ECD) with one V-type Ig-like domain, a 21 aa transmembrane (TM) domain, and a 35 aa cytoplasmic tail. TREM-2 forms a receptor signaling complex with TYROBP which mediates signaling and cell activation following ligand binding (PubMed:10799849). Acts as a receptor for amyloid-beta prote... | |||
TMPH-03038 |
Cobra venom factor Protein, Naja kaouthia, Recombinant (His & SUMO)
Cobra venom factor,Complement C3 homolog,CVFk,CVF |
Naja kaouthia | E. coli |
Complement-activating protein in cobra venom. It is a structural and functional analog of complement component C3b, the activated form of C3. It binds factor B (CFB), which is subsequently cleaved by factor D (CFD) to form the bimolecular complex CVF/Bb. CVF/Bb is a C3/C5 convertase that cleaves both complement components C3 and C5. Structurally, it resembles the C3b degradation product C3c, which is not able to form a C3/C5 convertase. Unlike C3b/Bb, CVF/Bb is a stable complex and completely re... | |||
TMPY-03749 |
LC3B Protein, Human, Recombinant (His)
microtubule-associated protein 1 light chain 3 beta,ATG8F,MA... |
Human | E. coli |
MAP1LC3B (Microtubule Associated Protein 1 Light Chain 3 beta, also known as LC3B) is a Protein Coding gene. The product of this gene is a subunit of neuronal microtubule-associated MAP1A and MAP1B proteins, which are involved in microtubule assembly and important for neurogenesis. LC3B is a member of the MAP1 LC3 family. It is most abundantly expressed in the heart, brain, skeletal muscle, and testis. LC3B is a subunit of the neuronal microtubule and functions in the formation of autophagosomal... | |||
TMPY-01711 |
Serpin B2 Protein, Human, Recombinant (GST)
PAI,serpin peptidase inhibitor, clade B (ovalbumin), member ... |
Human | Baculovirus Insect Cells |
Serpins are the largest and most diverse family of serine protease inhibitors which are involved in some fundamental biological processes such as blood coagulation, complement activation, fibrinolysis, angiogenesis, inflammation and tumor suppression and are expressed in a cell-specific manner.SerpinB2, also known as Plasminogen activator inhibitor 2, Placental plasminogen activator inhibitor, Monocyte Arg-serpin, Urokinase inhibitor and PAI2, is a cytoplasm protein that belongs to the serpin fa... | |||
TMPY-02519 |
BLVRB Protein, Human, Recombinant (His)
HEL-S-10,biliverdin reductase B,FLR,BVRB,SDR43U1 |
Human | E. coli |
Biliverdin reductase (hBVR) is a serine/threonine kinase that catalyzes reduction of the heme oxygenase (HO) activity product, biliverdin, to bilirubin. BVR consists of an N-terminal dinucleotide-binding domain (Rossmann-fold) and a C-terminal domain that contains a six-stranded β-sheet that is flanked on one face by several α-helices. The C-terminal and N-terminal domains interact extensively, forming the active site cleft at their interface. Biliverdin reductase (BVR) catalyzes the last step i... | |||
TMPY-01710 |
IkB alpha/NFKBIA Protein, Human, Recombinant (His)
IkB α,IKBA,nuclear factor of kappa light polypeptide gene en... |
Human | E. coli |
Nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor, alpha (IkB alpha, NFKBIA, or IKBA), is a member of the NF-kappa-B inhibitor family that function to inhibit the NF-kB transcription factor. NFKBIA inhibits NF-kB by masking the nuclear localization signals (NLS) of NF-kB proteins and keeping them sequestered in an inactive state in the cytoplasm. Also, NFKBIA blocks the ability of NF-κB transcription factors to bind to DNA, which is required for NF-kB's proper function... |