大连美仑生物技术有限公司

Apoptosis Bcl-2 Bcl-6 Caspase Ferroptosis Mdm2 p53 RIP kinase Survivin TNF-alpha Cuproptosis IAP Metabolic Enzyme/Protease PDHK ROS Kinase Phosphatase MDM-2/p53 Kinesin PKC HSP Autophagy TNF Receptor FKBP Bcl-2 Family Pyroptosis DAPK PKD EBV Glutathione Peroxidase Transferrin Receptor c-Myc Necroptosis ASK1 Thymidylate Synthase

Autophagy

Autophagy LRRK2 Estrogen/progestogen PINK1/Parkin Dynamin Anti-infection Oxidative Phosphorylation Akt AMPK JAK Toll-like Receptor (TLR) ULK p62 Atg8/LC3 Atg7 Atg4 AUTACs

Epigenetics

DNA Methyltransferase DNMT Epigenetic Reader Domain Histone Acetyltransferase Histone demethylases Histone Methyltransferase PKC AMPK HDAC JAK MicroRNA Protein Arginine Deiminase Phosphodiesterase (PDE)

GPCR/G Protein

Adenosine Receptor Angiotensin Receptor Cannabinoid Receptor CaSR E1 Activating CRFR E2 conjugating E3 Ligase Endothelin Receptor GHSR Glucagon Receptor GLP-1R GPCR19(TGR5) GPR GPR119 GPR40(FFAR1) Imidazoline Receptor Leukotriene Receptor LPA Receptor OX Receptor Protease-activated Receptor Rac Prostaglandin Receptor Oxytocin Receptor Ras Rho S1P Receptor Sigma Receptor 5-HT Receptor Neurokinin Receptor mAChR GCGR LPL Receptor Dopamine Receptor Guanylate Cyclase Histamine Receptor CXCR CCR GPR35 P2Y Receptor Opioid Receptor GPR68 mGluR Formyl Peptide Receptor (FPR) Platelet-activating Factor Rec GnRH Receptor Protease Activated Receptor (P Vasopressin Receptor Chemerin Receptor Melatonin Receptor MCHR1 (GPR24) Orexin Receptor (OX Receptor) RGS Protein CGRP Receptor Free Fatty Acid Receptor

Immunology/Inflammation

AhR CCR COX Complement 5(C5) CXCR Histamine Receptor IL Receptor Immunology IL-5 NOD1 IL-12 PD-1 IL-17 PDL-1 reactive oxygen species (ROS) NLRP3 TLR STING Toll-like Receptor (TLR) Bcr-Abl Salt-inducible Kinase (SIK) Glucocorticoid Receptor IRAK SphK Interleukin Related PGE synthase Macrophage migration inhibitor Complement System MyD88 FLAP Thrombopoietin Receptor Arginase NO Synthase AP-1 Nuclear Factor of activated T IFNAR CD276/B7-H3 CD3 CD38 CD28 CD22 CD20 CD19 Aryl Hydrocarbon Receptor PD-1/PD-L1 NOD-like Receptor (NLR) Mesothelin Mucin NTPDase PSMA SOD DOCK CD74 CD6 CD73 CTLA-4 CX3CR1 Cyclic GMP-AMP Synthase FAP Galectin Cyclophilin P-selectin CD2 CD47 Tim3 TROP2 Glycoprotein VI Kallikrein LAG-3 VAP-1 BCL6

Integrin

JAK-STAT/IL6

JAK STAT IL-6 Pim EGFR

MAPK

ErbB2 ERK JNK MEK p38 MAPK Mixed Lineage Kinase Raf

Membrane Transporter/Ion Chann

Amino acid transporter antagon ATPase Calcium Channel CFTR Chloride channel CRM1 GABA Receptor GluR iGluR NMDAR P-gp Potassium Channel Proton Pump SGLT Sodium Channel TRPV P-glycoprotein Na+/K+ ATPase Piezo Channel Fat Mass and Obesity-associate TRP Channel BCRP nAChR CRAC Channel Apical Sodium-Dependent Bile A P2X Receptor Monocarboxylate Transporter Na+/HCO3- Cotransporter GlyT OAT NKCC Monoamine Transporter HCN Channel EAAT Ferroportin GLUT Na+/H+ Exchanger (NHE) Na+/Ca2+ Exchanger FATP ATP Synthase ASCT VDAC Urea Transporter URAT1 Aquaporin Calmodulin

Metabolic Enzyme/Protease

5-alpha Reductase Aminopeptidase ATP-citrate lyase in Carbonic Anhydrase CETP DGAT DPP-4 Factor Xa FOX FXR Glucokinase(GK) GSNOR HCV Protease HIF HMG-CoA Reductase HSP IDO Lactate Dehydrogenase Integrase MMP NAMPT P450 PAI-1 PDE PGC-1α Phospholipase Procollagen C Protein Proteases PKM Proteasome RAR/RXR Retinoid Receptor Serine Protease Thrombin Transferase Xanthine Oxidase p38-MAPK Stearoyl-CoA Desaturase (SCD) Mitochondrial Metabolism (MPC) Tyrosinase Endogenous Metabolite Phosphatase Pyruvate Kinase PDI Phosphodiesterase (PDE) HIF/HIF Prolyl-Hydroxylase Hexokinase Ser/Thr Protease Carboxylesterase Cathepsin Cytochrome P450 Drug Metabolite E1/E2/E3 Enzyme Angiotensin-converting Enzyme HMG-CoA Reductase (HMGCR) Aldose Reductase Oxidative Phosphorylation NADPH Oxidase Lipoxygenase DAGL MAGL MALT1 Adenosine Kinase COMT Glutathione S-transferase Adenosine Deaminase Acyltransferase Enolase Aldehyde Dehydrogenase (ALDH) Farnesyl Transferase Glucosidase PDHK Fatty Acid Synthase (FASN) Dipeptidyl Peptidase Methylenetetrahydrofolate Dehy Dihydroorotate Dehydrogenase Renin FAAH SGK Dopamine β-hydroxylase HIV Integrase Adiponectin Receptor ROR LXR Mineralocorticoid Receptor REV-ERB Amine N-methyltransferase

Neuronal Signaling

5-HT Receptor AChR BACE Beta Amyloid Beta-secretase CaMK CGRP Receptor Dopamine Receptor FAAH Gamma-secretase GlyT iGluR MAO mAChR Opioid Receptor Serotonin Transporter Legumain γ-secretase Notch Monoamine Oxidase Trk Receptor Cholinesterase (ChE) Imidazoline Receptor Amyloid-β Dopamine Transporter Sigma Receptor Glucosylceramide Synthase (GCS

NF-κB

NF-κB Nrf2 IκB/IKK Reactive Oxygen Species Keap1-Nrf2 IKK RANKL/RANK

Others

Androgen Receptor Aromatase CD20 CD52 c-Myc CPT1 c-RET CTLA-4 Decarboxylase Dehydrogenase FPR GLUT Glutaminase HIV ProteaseAnti-infection HSP90 Hydroxylase IAP IgE IRE1 LDL Lipase Lipoxygenase Lysyl Hydroxylase MT Receptor NADPH oxidase others P2 Receptor PAFR PCSK9 RAAS RANK Ligand Reverse Transcriptase S6 Kinase Thioredoxin Tie-2 SARM Vasopressin Receptor VDA Vitamin D Related CDA TrxR PDE IDO

PI3K/Akt/mTOR

Akt MELK mTOR GSK-3 PDK-1 PI3K PIKfyve PTEN RSK AMPK PI4K PIN1

Protein Tyrosine Kinase/PTK

ACK ALK Axl Bcr-Abl BTK cAMP(PKA) c-Kit c-Met CSF-1R DYRK EGFR Ephrin receptor FAK FGFR FLT3 HER2 IGF-1R MET Insulin Receptor PDGFR PKA ROS Src Syk Trk receptor VEGFR

Stem Cell /Wnt

c-Jun Hedgehog/Smoothened Hippo pathway Met stemness kinase OCT Wnt/β-catenin Adenylate Cyclase YAP PKA TGF-beta/Smad Gli Wnt sFRP-1 Smo Organoid Hedgehog Porcupine PKG Hippo (MST) Oct3/4 β-catenin BMI1

TGF-beta/Smad

TGF-beta/Smad TGF-β Receptor PKC PKA

Cell Cycle/DNA Damage

Antifolate APC ATM/ATR Aurora Kinase BMI-1 Casein Kinase CDK CD38 Chk DHFR DNA alkylator DNA-PK DNA/RNA Synthesis DUB Dynamin HDAC HSP Kinesin Microtubule Associated p97 MTH1 PAK PERK PLK PPAR PARP ROCK Sirtuin RAD51 Telomerase TOPK Topoisomerase Wee1 Deubiquitinase NEKs OGG Polo-like Kinase (PLK) Microtubule/Tubulin Mps1 MASTL Haspin Kinase SRPK DNA Alkylator/Crosslinker ATF6 Checkpoint Kinase (Chk) G-quadruplex Nucleoside Antimetabolite/Anal Eukaryotic Initiation Factor ( CRISPR/Cas9 IRE1 MARK Epoxide Hydrolase

Protein Tyrosine Kinase/RTK

TAM Receptor ROS Kinase JAK Src VEGFR c-Met Syk ALK FAK IGF-1R FLT3 c-Met/HGFR PDGFR Bcr-Abl c-Fms Ephrin receptor FLT3 BTK Itk Anaplastic lymphoma kinase (AL Ack1 RET c-Kit FGFR EGFR Insulin Receptor Discoidin Domain Receptor BRK BMX Kinase SHP2 DYRK Tie Pyk2 GDNF Receptor

Epigenetics Histone

Methyltransferase

Anti-infection

HSV Flavivirus others Fungal Parasite HBV Bacterial Dengue virus HIV Filovirus Antibiotic VSV SARS-CoV Beta-lactamase HCV CMV Reverse Transcriptase Influenza Virus Arenavirus HIV Protease

MAPK/ERK Pathway

ERK p38 MAPK MEK MAP3K Ribosomal S6 Kinase (RSK) Raf JNK MAP4K KLF Mixed Lineage Kinase MNK

Vitamin D Related/Nuclear Rece

Estrogen Receptor/ERR Progesterone Receptor VD/VDR Androgen Receptor Thyroid Hormone Receptor Nuclear Hormone Receptor 4A/NR Constitutive Androstane Recept

Cytoskeleton

MARCKS Integrin Gap Junction Protein Myosin Polo-like Kinase (PLK) Annexin A Dynamin Arp2/3 Complex

Antibodydrug Conjugate/ADC Rel

ADC Cytotoxin Antibody-Drug Conjugates (ADCs Drug-Linker Conjugates for ADC

PROTAC

Molecular Glues PROTACs Ligands for Target Protein for PROTAC Linkers Ligands for E3 Ligase E3 Ligase Ligand-Linker Conjug PROTAC-Linker Conjugates for P Target Protein Ligand-Linker C SNIPERs LYTACs AUTOTACs

通用试剂类

氨基酸

氨基酸犬尿氨酸系列

胆酸系列

蛋白及衍生物

合成多肽

核酸及其衍生物

抗生素及抗病毒

抗生素及抗病毒抗真菌抗生素抗细菌抗生素抗肿瘤抗生素抗病毒化合物

酶辅酶

染色剂指示剂

生物缓冲剂

碳水化合物

碳水化合物多糖寡糖去垢剂

通用试剂

微生物检测

微生物培养基

维生素

显色及标记试剂

植物生长激素

其他生化试剂

其他生化试剂表面活性剂无机盐

还原剂

蛋白修饰

交联剂

表面活性剂/去垢剂

非离子表活剂/去垢剂阴离子表活剂/去垢剂阳离子表活剂/去垢剂

生物耗材

吸头类

常规吸头滤芯吸头（PCR用）

PCR类

离心管类

常规离心管

细胞培养类

细胞培养板细胞培养皿细胞冻存培养瓶

液体处理类

移液管

体外诊断

核心原料

亲和素

重组蛋白

IgG-Fc

植物研究相关

植物激素

赤霉素类(GA) 细胞分裂素(CTK) 油菜素甾醇(BR) 其他植物激素脱落酸（ABA）乙烯(ETH)

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Bevacizumab

总货号: MB2791

货号	规格	发货时间
MB2791-1	1MG/只 [￥800.00] :￥800.00	现货
MB2791-2	5MG/只 [￥3200.00] :￥3200.00	现货

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摩尔浓度计算器

相关论文

分子量：146.5 KDa

简介：Bevacizumab（贝伐单抗）是一种抗VEGF的人源化IgG1单克隆抗体，通过高亲和力且特异性地与所有 VEGF-A异构体结合，抑制其与VEGFR-1和VEGFR-2的相互作用，进而抑制血管生成。Bevacizumab是一种靶向治疗药物，称为血管生成抑制剂，可用于研究和治疗多种类型的癌症。

产品形式：蛋白原液，装于冻存管中，单抗质量为标示数量1mg或者5mg，体积根据不同批次浓度不同略有不同，具体批次浓度请详见COA。

别名：贝伐单抗; 贝伐珠单抗; Anti-Human VEGF, Humanized Antibody

物理性质和指标：

外观：……………….......Liquid

克隆类型：………….......重组抗体

表达系统：………….......HEK293 supernatant

亚型：……………….......Human IgG1

储存缓冲液：………..…..Acetic acid buffer, pH5.4 with protectants

浓度：……………….......见COA

纯度：……………..........Non-reduced SDS-PAGE：≥95%；SEC-HPLC：≥95%

内毒素：……………...…Less than 5 EU/mg by LAL method

Biological Activity：……Corresponds to reference standard

产品用途：科研试剂，广泛应用于分子生物学、药理学等科研方面，严禁用于人体。Bevacizumab的核心作用是抑制异常血管生成（阻断VEGF介导的血管内皮细胞增殖、迁移，减少血管渗漏），主要用于肿瘤研究，如：结直肠癌、非小细胞肺癌、胶质母细胞瘤、肾细胞癌、卵巢癌、宫颈癌、输卵管癌、腹膜癌等。另外在某些眼底血管异常增生相关疾病中，Bevacizumab可抑制眼底新生血管渗漏，如湿性年龄相关性黄斑变性（wAMD）、糖尿病性黄斑水肿（DME）、视网膜静脉阻塞（RVO）继发的黄斑水肿。

储存条件：-70±15℃避光保存。首次使用后建议分装，避免反复冻融。

运输条件：干冰运输

生物活性：

Target

VEGFA

体外研究

Bevacizumab(2-4mg/mL)低浓度水平处理HHT患者鼻内内皮细胞，24h后显著降低了VEGF的表达，但在48h后再次升高，且超过4mg/mL时会产生细胞毒性作用。

Bevacizumab(5- 1000ng/mL)处理U87-RFP细胞48h后，不会引起细胞死亡。

体内研究

Bevacizumab(5和25 mg/kg)通过腹腔注射治疗原位胶质瘤小鼠，显著抑制了肿瘤血管生长速率，提高了存活率。

Bevacizumab(5mg/kg)腹膜给药可以延长卵巢癌模型小鼠的生存期。

Bevacizumab(5mg/kg)治疗骨肉瘤模型小鼠，表现出较强的抗血管生成活性。

使用方法：请详见说明书

【注意】

●本产品为无菌包装，使用时请注意无菌操作，防止污染。

●为了您的安全和健康，请穿实验服并戴一次性手套操作。

●部分产品我司仅能提供部分信息，我司不保证所提供信息的权威性，以上数据仅供参考交流研究之用。

参考文献：

[1]. Tan H, et al. 99mTc-labeled bevacizumab for detecting atherosclerotic plaque linked to plaque neovascularization and monitoring antiangiogenic effects of treatment in ApoE-/-mice. Sci Rep. 2017 Jun 14;7(1):3504.

[2]. Haneen Sadick, Elena SchÄfer, Christel Weiss, et al. An in vitro study on the effect of bevacizumab on endothelial cell proliferation and VEGF concentration level in patients with hereditary hemorrhagic telangiectasia[J].Experimental and Therapeutic Medicine.July 5, 2022.11493.

[3]. Von Baumgarten L , Brucker D , Tirniceru A ,et al. Bevacizumab Has Differential and Dose-Dependent Effects on Glioma Blood Vessels and Tumor Cells[J].Clinical Cancer Research, 2011, 17(19):6192-205.

[4]. Mabuchi S , Terai Y , Morishige K ,et al.Maintenance treatment with bevacizumab prolongs survival in an in vivo ovarian cancer model.[J]Clinical Cancer Research , 2008, 14(23):7781-9.

[5]. Zhao Z X , Li X , Liu W D , et al. Inhibition of Growth and Metastasis of Tumor in Nude Mice after Intraperitoneal Injection of Bevacizumab[J]. Orthopaedic Sugery. 2016.234-240.

生物活性数据展示：

Immoblized VEGF165 Protein at 0.5μg/mL binding to Bevacizumab (Meilunbio, Cat:MB2791), and tested by anti-Human IgG Fc Antibody[HRP] at 1:5000. The binding EC₅₀ is 0.318nM and converts to 46.514 ng/mL.

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我司所售出产品仅供于科研研究用途（非临床科研研究），每次销售产品行为都适用于我司网上所列明的通用销售条款。

CAS号：216974-75-3

别名：贝伐单抗; Anti-Human VEGF, Humanized Antibody

质量标准：>95%,蛋白原液

摩尔浓度计算器（本计算器可帮助您计算出特定溶液中溶质的质量、溶液浓度和体积之间的关系）

摩尔浓度计算公式：质量 (g) = 浓度 (mol/L) x 体积 (L) x 分子量 (g/mol)

质量（g）

浓度 (mol/L)

体积 (L)

分子量 (g/mol)