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Search Results for " bk "

46

抑制剂 & 化合物

3

天然产物

8

重组蛋白

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Cat. No.	Product Name	Target	Signaling Pathways
T26830	BK 129 BK-129,BK129
	BK 129 is a local anesthetic with relaxant properties. BK 129 inhibits Ca2+ entry into the smooth muscle cell and Ca2+ release from sarcoplasmic reticulum.
T30481	BK 218 BK218,BK-218
	BK 218 is a novel cephalosporin, which is active against streptococcus pneumoniae, Haemophilus influenza, and Moraxella catarrase, but has a higher MIC against penicillin-resistant strains. Bk-218 has dual administration routes and the activity spectrum m
T72905	cyclo(RLsKDK) BK-1361
	Cyclo(RLsKDK) (BK-1361) 作为ADAM8金属蛋白酶的特异性抑制剂，展示出182 nM的IC50值。其在炎性疾病和癌症治疗中显示出潜在的应用价值。
T24986	6bK 6 bK,6-bK,IDE inhibitor 6bK,IDE-IN-6bK,IDE-inhibitor-6bK
	6bK is an inhibitor of insulin degrading enzyme (IDE).
T20782	Triazinetriethanol Grotan BK,Grotan,Actane
	Triazinetriethanol is a bactericidal agent used in coolant liquids.
T30650	C.I. 15690 Chrome Black BK,Eriochrome Black SR
	C.I. 15690 is a dye.
T8747	Levofloxacin hydrochloride	DNA gyrase; Topoisomerase	DNA Damage/DNA Repair
	Levofloxacin hydrochloride 是一种广谱的第三代氟喹诺酮类抗生素，是氧氟沙星的光学活性 L-异构体，具有抗菌活性。左氧氟沙星通过细菌细胞壁扩散并通过抑制 DNA 促旋酶（细菌拓扑异构酶 II）起作用，这是一种 DNA 复制、RNA 转录和细菌 DNA 修复所需的酶。 DNA 促旋酶活性的抑制导致细菌细胞生长受阻。
T83688	R 715 TFA [Ac-Lys-[D-βNal7,Ile8]des-Arg9]-BK,Ac-Lys-Arg-Pro-Pro-Gly-Phe-Ser-D2Nal-Ile-OH
	R 715是一种布拉迪肾上腺素B1受体拮抗剂。它抑制在表达布拉迪肾上腺素B1受体的孤立人类脐带中由布拉迪肾上腺素引发的收缩（pA2 = 8.49）。R 715（200、400及600 µg/kg）通过尾部闪烁测试减少了由链脲佐菌素（STZ）诱导的糖尿病神经病变小鼠模型中尾部撤回的潜伏期。它还在以髓磷脂少突胶质细胞糖蛋白（MOG）（35-55）（MOG35-55）抗原肽诱导的实验性自体免疫性脑炎（EAE）小鼠模型中，通过每天1 mg/kg的剂量减少了后肢无力和瘫痪的发病率，改善对称步态，并减少脊髓炎症灶点数、神经元脱髓鞘以及病灶单核细胞侵袭。R 715（0.01 nmol/动物，脑室内）能在自发性高血压大鼠中降低平均动脉血压并增加心率。
T78982	BK60106	Apoptosis	Apoptosis
	BK60106是一种选择性针对CD99的抑制剂，能够直接与CD99的胞外结构域结合。它能特异性地诱导尤文肉瘤(ES)细胞凋亡(apoptosis)，而且伴随的DNA损伤相对较少。
T74865	BK50164
	BK50164 是一种有效的CD73抑制剂，IC50值为 13.089 µM。BK50164 与 CD99 结合KD 值为 1.5 µM。BK50164 显示抗增殖活性。BK50164 诱导细胞凋亡 (Apoptosis) 和细胞周期停滞在 Sub-G1 阶段。
T1451	Levofloxacin hydrate 左氧氟沙星半水合物,Levaquin hydrate,Cravit hydrate,Quixin hydrate,Levofloxacin Hemihydrate,Tavanic hydrate,Iquix hydrate	DNA gyrase; Topoisomerase; Antibacterial; Antibiotic	DNA Damage/DNA Repair; Microbiology/Virology
	Levofloxacin hydrate (Cravit hydrate) 是抗生素化合物，抑制细菌DNA 旋转酶活性。
T6060L	Anabasine HCl BB-NC-0036,CCG-38440,H-8174,AR-1H7273,ZX-BK000320,ST-24041653
	Anabasine HCl is used as a clinical biomarker for tobacco smoke exposure and as an insecticide. It is also a depolarizing NMJ blocker, aromatase inhibitor, nAChr antagonist, and teratogen found in species of Nicotiana.
T36095	Histone H2BK12ac (1-22)-GGK-biotin amide (trifluoroacetate salt) Histone H2BK12ac (1-22)-GGK-biotin amide (trifluoroacetate salt)
	Histone H2BK12ac (1-22)-GGK-biotin amide (trifluoroacetate salt) 可用于生命科学领域的相关研究，其产品编号为 T36095。
T7951	TBK1/IKKε-IN-5	IκB/IKK	NF-κB
	TBK1/IKKε-IN-5 是一种 TBK1 (IC50:1 nM) 和 IKKε (IC50:5.6 nM) 的双抑制剂。
T15559	TBK1/IKKε-IN-2	IκB/IKK	NF-κB
	TBK1/IKKε-IN-2 是双重TBK1和IKKε抑制剂。
T73322	TBK1-IN-1	IκB/IKK	NF-κB
	TBK1-IN-1 是一种具有特异性和高效性的 TANK 结合激酶 1 (TBK1) 抑制剂（IC50: 22.4 nM），具有抗癌活性。TBK1-IN-1 对 TBK1 下游靶基因 cxcl10 和 ifnβ 的表达有抑制作用。
T60086	TTBK1-IN-2 N-[4-(4-chlorophenoxy)phenyl]-7H-pyrrolo[2,3-d]pyrimidin-4-amine	Microtubule Associated	Cytoskeletal Signaling
	TTBK1-IN-2 (N-[4-(4-chlorophenoxy)phenyl]-7H-pyrrolo[2,3-d]pyrimidin-4-amine) 是 Tau-Tubulin 激酶 (TTBK1) 的抑制剂，IC50 为 0.24 和 4.22 µM。 TTBK1-IN-2 降低细胞培养物和转基因 TDP-43 小鼠脊髓中的 TDP-43 磷酸化。
T75107	CrBKA
	CrBKA 是SIRT6的弱活性荧光小分子底物。
T26833	BKM-570
	BKM-570, a bradykinin antagonist, causes impressive growth inhibition of lung and prostate tumors.
T26831	BKM1644 BKM 1644,BKM-1644
	BKM1644 is an effective inhibition of the proliferation of metastatic, castration-resistant PCa (mCRPC) cells.
T38263	TBK1/IKKε-IN-4 TBK1/IKKε-IN-4
	TBK1/IKKε-IN-4 is a 6-aminopyrazolopyrimidine derivative and a potent, selective TBK1 and IKKε inhibitor with IC50 values of 13 nM and 59 nM, respectively. TBK1/IKKε-IN-4 shows 100- to 1000-fold less activity against other protein kinases including PDK1, PI3K family members and mTOR[1]. TBK1/IKKε-IN-4 (Compound II; 96 hours; A549 andHCC44 cells) treatmentdisplays selective toxicity in TBK1-dependent cancer cell lines (IC50 of ~ 4.2 μM for H441 cells and IC50 of ~0.4 μM for A549 cells)[1].TBK1/IK...
T72808	(R)-TTBK1-IN-1
	TTBK1-IN-1 是一种强效、选择性、脑渗透型 tau 微管蛋白激酶 1 (TTBK1) 抑制剂。(R)-TTBK1-IN-1 是 TTBK1-IN-1 的对映体。TTBK1-IN-1 可用于阿尔茨海默病及相关疾病的研究。
T38598	CBK289001
	CBK289001 is a tartrate-resistant acid phosphatase (TRAP/ACP5) inhibitor. CBK289001 inhibits TRAP 5b MV , TRAP 5b OX and TRAP 5a OX with IC 50 s of 125 μM, 4.21 μM and 14.2 μM, respectively.
T36247	TBK1 control PROTAC® 4
	Negative control for TBK1 PROTAC 3i. Binds TBK1 with high affinity, but exhibits no significant degradation of TBK1. PROTAC is a registered trademark of Arvinas Operations, Inc., and is used under license.
T40348	TTBK1-IN-1 TTBK1-IN-1
	TTBK1-IN-1 is a highly potent and selective inhibitor of tau tubulin kinase 1 (TTBK1), capable of penetrating the blood-brain barrier with ease. With an IC 50 value of 2.7 nM, TTBK1-IN-1 exhibits strong inhibitory activity against TTBK1. This compound holds great promise for advancing research in Alzheimer's disease and other tauopathies.
T13097	TBK1/IKKε-IN-1	IκB/IKK	NF-κB
	TBK1/IKKε-IN-1 is a dual inhibitor of TBK1 and IKKε (IC50s of <100 nM).
T39841	TBK1/IKKε-IN-6 TBK1/IKKε-IN-6
	TBK1/IKKε-IN-6 (example 110) is a potent inhibitor of TBK1 and IKKε, with IC50 values of less than 100 nM for both enzymes.
T10556	BKI-1369	EGFR	Angiogenesis; JAK/STAT signaling; Tyrosine Kinase/Adaptors
	BKI-1369 is a bumped kinase inhibitor. BKI-1369 increases hERG-inhibitory activity (IC50:1.52 μM).
T26832	BKM1740 BKM-1740,BKM 1740
	BKM1740 induced apoptosis in prostate cancer (PCa) cells by repressing survivin at both the mRNA and protein levels in vitro.
T16370	OABK hydrochloride	Others	Others
	OABK hydrochloride is a small-molecule switch. It also can be used to control protein activity.
T28222	5-Hydroxy-1-methylhydantoin HD-003,HD003,5-羟基-1-甲基咪唑啉-2,4-二酮,NZ419,NZ-419,HD 003,NZ 419	Bradykinin Receptor	GPCR/G Protein
	5-Hydroxy-1-methylhydantoin (HD-003) 是一种可能用于治疗肾衰竭的抗氧化剂。它是肌酐代谢物，是一种羟基自由基清除剂，此前已显示通过抑制大鼠慢性肾病的进展来提供肾脏保护。它是一种新型抗氧化药物，可完全抑制 B2-激肽受体(B2KR) 对 VSMC 中高葡萄糖 (25 mM) 刺激的反应，并且还显示可减弱 BK 对 VSMC 重塑的影响。它抑制 BK 诱导的 MAPK 磷酸化增加并减弱 VSMC 中结缔组织生长因子 (CTGF) 蛋白水平的增加。这些研究结果表明，它可能通过其抗氧化特性赋予血管保护免受高葡萄糖浓度和 BK 刺激以改善血管损伤和重塑。
T4612	NS309	EGFR; Potassium Channel; HER	Angiogenesis; JAK/STAT signaling; Membrane transporter/Ion channel; Tyrosine Kinase/Adaptors
	NS309 是选择性钙依赖性钾离子通道 SK/IK 的激活剂，在 BK 通道上没有激活作用。
T3102	NS-1619	Apoptosis; Potassium Channel	Apoptosis; Membrane transporter/Ion channel
	NS 1619 是 Ca2+激活的 K+(BK) 通道的激活剂，是一种高效的松弛剂，在血管和其他组织的几个平滑肌中的 EC50约为 10 – 30 μM。它抑制A2780卵巢癌细胞增殖并诱导细胞凋亡。
T12255	NS19504	Potassium Channel	Membrane transporter/Ion channel
	NS19504 是 Ca2+激活的 K+通道激活剂 (EC50=11.0 µM)，对膀胱平滑肌自发性相位收缩具有松弛作用。
T24065	FK-3657 FK 3657,FK3657,FR-173657,FR 173657,FR173657
	FK-3657 is a non-peptide antagonist of bradykinin (BK)-B2 receptor.
T24137	HENA
	HENA is a novel activator of large conductance, voltage- and Ca2+-gated K+ (BK) channels.
T37294	GoSlo-SR-5-69
	BK channel activator (EC50 = 251 nM). Shifts the voltage required for half maximal negatively (DV1/2 = -104 mV).
T40650	Dihydroisopimaric acid
	Dihydroisopimaric acid activates BK channels alphabeta1, which are large conductance Ca 2+ activated K + channels. This compound directly measures the opening of BKalphabeta1 under a whole-cell voltage clamp.
TP1725	Bradykinin (1-5)
	Bradykinin (1-5) is a major stable metabolite of Bradykinin, formed by the proteolytic action of angiotensin-converting enzyme (ACE).The bradykinin (BK) fragment (1-5) (RPPGF) is among the most stable of naturally occurring metabolites. Bradykinin (1-5) m
T75998	cyclo(RLsKDK) TFA
	cyclo(RLsKDK) (TFA) (BK-1361 (TFA)) 是一种特异性的金属蛋白酶 ADAM8抑制剂，IC50值为 182 nM。cyclo(RLsKDK) (TFA) 在炎性疾病和癌症中有潜在应用。
T70224	Bupivacaine tartrate
	Bupivacaine is a BK/SK, Kv1, Kv3, TASK-2 K Channel and voltage-gated Na channel blocker used as an anesthetic. It maybe neurotoxic at high does, inducing apoptosis in neuroblastoma cells. It acts by binding to the intracellular portion of voltage-gated sodium channels and blocking sodium influx into nerve cells.
T40750	12,14-Dichlorodehydroabietic acid
	12,14-Dichlorodehydroabietic acid, a chlorinated resin acid, exhibits potent calcium-activated potassium (BK) channel opening activity. It effectively inhibits GABA-dependent chloride influx in the mammalian brain, functioning as a non-competitive antagonist of GABA A receptors. Moreover, 12,14-Dichlorodehydroabietic acid induces an elevation in cytosolic free calcium levels and promotes the release of neurotransmitters.
T76169	Angiotensin-converting enzyme
	Angiotensin-converting enzyme (ACE)血管紧张素转换酶是一种二羧基肽酶，它将非活性的血管紧张素 I (Ang I) 转化为活性的 Ang II，并降解活性的缓激肽 (BK)。Angiotensin-converting enzyme 是一种有效的血管收缩剂，常用于生化研究。
T37808	Kaliotoxin
	aliotoxin是神经BK型肽基的抑制剂，对Kv通道和钙激活的钾通道能产生特异性抑制。Kaliotoxin对细胞膜电位和神经元兴奋性的调控具有研究意义。其产品编号为 T37808，CAS号为 145199-73-1
T83868	(±)13,14-EDT (±)13,14-Epoxydocosatrienoic Acid,(±)13,14-EpDoTrE,(±)-Dihomo-13,14-EET
	(±)13,14-EDT是一种氧脂和腎上腺酸的代谢产物，通过细胞色素P450（CYP）途径形成。在50 nM的浓度下，它能激活分离的大鼠冠状小动脉平滑肌细胞中的大导电钙激活钾通道（KCa1.1/BK），并导致分离的猪小动脉扩张（EC50 = 12 pM）。(±)13,14-EDT还能使用TP受体激动剂U-46619预收缩的分离牛冠状动脉放松。
T36215	17R(18S)-EpETE
	17R(18S)-EpETE is an oxylipin and a cytochrome P450 metabolite of eicosapentaenoic acid .1,217R(18S)-EpETE is an activator of large-conductance calcium-activated potassium (BKCa) channels, increasing the potassium current amplitude by 15-fold in isolated rat cerebral artery vascular smooth muscle cells (VSMCs) at +60 mV when used at a concentration of 50 nM.2It has negative chronotropic effects in isolated neonatal rat cardiomyocytes (NRCMs; EC50= ~1-2 nM) and prevents calcium-induced increases ...

化合物

Cat.No: T26830

Synonym: BK-129,BK129

Cat.No: T30481

Synonym: BK218,BK-218

Cat.No: T72905

Synonym: BK-1361

Cat.No: T24986

Synonym: 6 bK,6-bK,IDE inhibitor 6bK,IDE-IN-6bK,IDE-inhibitor-6bK

Triazinetriethanol

Cat.No: T20782

Synonym: Grotan BK,Grotan,Actane

Cat.No: T30650

Synonym: Chrome Black BK,Eriochrome Black SR

Levofloxacin hydrochloride

Cat.No: T8747

Target: DNA gyrase, Topoisomerase

Cat.No: T83688

Synonym: [Ac-Lys-[D-βNal7,Ile8]des-Arg9]-BK,Ac-Lys-Arg-Pro-Pro-Gly-Phe-Ser-D2Nal-Ile-OH

Cat.No: T78982

Target: Apoptosis

Cat.No: T74865

Levofloxacin hydrate

Cat.No: T1451

Synonym: 左氧氟沙星半水合物,Levaquin hydrate,Cravit hydrate,Quixin hydrate,Levofloxacin Hemihydrate,Tavanic hydrate,Iquix hydrate

Target: DNA gyrase, Topoisomerase, Antibacterial, Antibiotic

Cat.No: T6060L

Synonym: BB-NC-0036,CCG-38440,H-8174,AR-1H7273,ZX-BK000320,ST-24041653

Histone H2BK12ac (1-22)-GGK-biotin amide (trifluoroacetate salt)

Cat.No: T36095

Synonym: Histone H2BK12ac (1-22)-GGK-biotin amide (trifluoroacetate salt)

TBK1/IKKε-IN-5

Cat.No: T7951

Target: IκB/IKK

TBK1/IKKε-IN-2

Cat.No: T15559

Target: IκB/IKK

Cat.No: T73322

Target: IκB/IKK

Cat.No: T60086

Synonym: N-[4-(4-chlorophenoxy)phenyl]-7H-pyrrolo[2,3-d]pyrimidin-4-amine

Target: Microtubule Associated

Cat.No: T75107

Cat.No: T26833

Cat.No: T26831

Synonym: BKM 1644,BKM-1644

TBK1/IKKε-IN-4

Cat.No: T38263

Synonym: TBK1/IKKε-IN-4

Cat.No: T72808

Cat.No: T38598

TBK1 control PROTAC® 4

Cat.No: T36247

Cat.No: T40348

Synonym: TTBK1-IN-1

TBK1/IKKε-IN-1

Cat.No: T13097

Target: IκB/IKK

TBK1/IKKε-IN-6

Cat.No: T39841

Synonym: TBK1/IKKε-IN-6

Cat.No: T10556

Target: EGFR

Cat.No: T26832

Synonym: BKM-1740,BKM 1740

OABK hydrochloride

Cat.No: T16370

Target: Others

5-Hydroxy-1-methylhydantoin

Cat.No: T28222

Synonym: HD-003,HD003,5-羟基-1-甲基咪唑啉-2,4-二酮,NZ419,NZ-419,HD 003,NZ 419

Target: Bradykinin Receptor

Cat.No: T4612

Target: EGFR, Potassium Channel, HER

Cat.No: T3102

Target: Apoptosis, Potassium Channel

Cat.No: T12255

Target: Potassium Channel

Cat.No: T24065

Synonym: FK 3657,FK3657,FR-173657,FR 173657,FR173657

Cat.No: T24137

Cat.No: T37294

Dihydroisopimaric acid

Cat.No: T40650

Bradykinin (1-5)

Cat.No: TP1725

cyclo(RLsKDK) TFA

Cat.No: T75998

Bupivacaine tartrate

Cat.No: T70224

12,14-Dichlorodehydroabietic acid

Cat.No: T40750

Angiotensin-converting enzyme

Cat.No: T76169

Cat.No: T37808

Cat.No: T83868

Synonym: (±)13,14-Epoxydocosatrienoic Acid,(±)13,14-EpDoTrE,(±)-Dihomo-13,14-EET

Cat.No: T36215

Cat. No.	Product Name	Target	Signaling Pathways
T6567	Levofloxacin Levaquin,Cravit,Tavanic,Fluoroquinolone,左氧氟沙星,(-)-Ofloxacin	Topoisomerase; Antibacterial; Antibiotic	DNA Damage/DNA Repair; Microbiology/Virology
	Levofloxacin (Fluoroquinolone) 是合成的氟喹诺酮类抗生素，有抑制细菌DNA 旋转酶的超螺旋活性的作用，能阻止DNA 复制。
T12373	Paxilline	Others	Others
	Paxilline is an indole alkaloid mycotoxin from Penicillium paxilli, acts as a potent BK channels inhibitor by an almost exclusively closed-channel block mechanism. Paxilline possesses significant anticonvulsant activity.
T12403	Penitrem A	Others	Others
	Penitrem A is a selective antagonist of BK channel with antiproliferative and anti-invasive activities against multiple malignancies.

天然产物

Cat.No: T6567

Synonym: Levaquin,Cravit,Tavanic,Fluoroquinolone,左氧氟沙星,(-)-Ofloxacin

Target: Topoisomerase, Antibacterial, Antibiotic

Cat.No: T12373

Target: Others

Cat.No: T12403

Target: Others

Species：

Expression System：

Tag：

Cat. No.	Product Name	Species	Expression System
TMPY-01598	Kininogen 1 Protein, Human, Recombinant (His) kininogen 1,KNG,BK,BDK	Human	HEK293 Cells
	Kininogen 1 Protein, Human, Recombinant (His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 71.3 kDa and the accession number is P01042-1.
TMPH-00201	BK polyomavirus (BKPyV) VP2 Protein (His) Minor capsid protein VP2,Minor structural protein VP2	BKPyV	E. coli
	Isoform VP2 is a structural protein that resides within the core of the capsid surrounded by 72 VP1 pentamers. Participates in host cell receptor binding together with VP1. Following virus endocytosis and trafficking to the endoplasmic reticulum, VP2 and VP3 form oligomers and integrate into the endoplasmic reticulum membrane. Heterooligomer VP2-VP3 may create a viroporin for transporting the viral genome across the endoplasmic reticulum membrane to the cytoplasm. Nuclear entry of the viral DNA ...
TMPH-00200	BK polyomavirus (BKPyV) VP1 Protein (His & Myc) Major structural protein VP1,Major capsid protein VP1	BKPyV	E. coli
	BK polyomavirus (BKPyV) VP1 Protein (His & Myc) is expressed in E. coli expression system with N-10xHis and C-Myc tag. The predicted molecular weight is 45.1 kDa and the accession number is P03088.
TMPH-01531	IKBKB Protein, Human, Recombinant (His)	Human	Baculovirus Insect Cells
	Serine kinase that plays an essential role in the NF-kappa-B signaling pathway which is activated by multiple stimuli such as inflammatory cytokines, bacterial or viral products, DNA damages or other cellular stresses. Acts as part of the canonical IKK complex in the conventional pathway of NF-kappa-B activation. Phosphorylates inhibitors of NF-kappa-B on 2 critical serine residues. These modifications allow polyubiquitination of the inhibitors and subsequent degradation by the proteasome. In tu...
TMPY-04769	RBKS Protein, Human, Recombinant (His) ribokinase,RBSK	Human	E. coli
	RBKS Protein, Human, Recombinant (His) is expressed in E. coli expression system with His tag. The predicted molecular weight is 36.4 kDa and the accession number is Q9H477-1.
TMPH-01532	IKBKB Protein, Human, Recombinant (E. coli, His)	Human	E. coli
	Serine kinase that plays an essential role in the NF-kappa-B signaling pathway which is activated by multiple stimuli such as inflammatory cytokines, bacterial or viral products, DNA damages or other cellular stresses. Acts as part of the canonical IKK complex in the conventional pathway of NF-kappa-B activation. Phosphorylates inhibitors of NF-kappa-B on 2 critical serine residues. These modifications allow polyubiquitination of the inhibitors and subsequent degradation by the proteasome. In tu...
TMPY-04547	PBK/TOPK Protein, Human, Recombinant (His) HEL164,Nori-3,CT84,TOPK,PDZ binding kinase,SPK	Human	Baculovirus Insect Cells
	PDZ binding kinase (PBK), also known as TOPK (T-LAK cell-originated protein kinase), is a serine/threonine kinase related to the dual specific mitogen-activated protein kinase kinase (MAPKK) family, and has all the characteristic protein kinase subdomains and a C-terminal PDZ-binding T/SXV motif. PBK is expressed in the testis restrictedly expressed in outer cell layer of seminiferous tubules, as well as placenta. PBK may be enrolled in the activation of lymphoid cells and support testicular fun...
TMPH-02180	TTBK2 Protein, Human, Recombinant (His & Myc)	Human	E. coli
	Serine/threonine kinase that acts as a key regulator of ciliogenesis: controls the initiation of ciliogenesis by binding to the distal end of the basal body and promoting the removal of CCP110, which caps the mother centriole, leading to the recruitment of IFT proteins, which build the ciliary axoneme. Has some substrate preference for proteins that are already phosphorylated on a Tyr residue at the +2 position relative to the phosphorylation site. Able to phosphorylate tau on serines in vitro.

重组蛋白

Kininogen 1 Protein, Human, Recombinant (His)

Cat.No: TMPY-01598

Species: Human

Expression System: HEK293 Cells

BK polyomavirus (BKPyV) VP2 Protein (His)

Cat.No: TMPH-00201

Species: BKPyV

Expression System: E. coli

BK polyomavirus (BKPyV) VP1 Protein (His & Myc)

Cat.No: TMPH-00200

Species: BKPyV

Expression System: E. coli

IKBKB Protein, Human, Recombinant (His)

Cat.No: TMPH-01531

Species: Human

Expression System: Baculovirus Insect Cells

RBKS Protein, Human, Recombinant (His)

Cat.No: TMPY-04769

Species: Human

Expression System: E. coli

IKBKB Protein, Human, Recombinant (E. coli, His)

Cat.No: TMPH-01532

Species: Human

Expression System: E. coli

PBK/TOPK Protein, Human, Recombinant (His)

Cat.No: TMPY-04547

Species: Human

Expression System: Baculovirus Insect Cells

TTBK2 Protein, Human, Recombinant (His & Myc)

Cat.No: TMPH-02180

Species: Human

Expression System: E. coli

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