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Search Results for " c7 "

Targets Recommended: Others

78

抑制剂 & 化合物

13

重组蛋白

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Cat. No.	Product Name	Target	Signaling Pathways
T40004	Pomalidomide-C7-NH2 hydrochloride	Others	Others
	Pomalidomide-C7-NH2 hydrochloride 是一种合成的 E3 连接酶配体-接头偶联物，它结合了 PROTAC 技术中使用的基于 Pomalidomide 的 CRBN 配体和接头。
T39701	Pomalidomide-C7-COOH Pomalidomide-C7-COOH
	Pomalidomide-C7-COOH is a chemically synthesized E3 ligase cereblon ligand-linker conjugate, utilized as an intermediate compound for the synthesis of PROTAC BCL-XL degraders.
T39645	Thalidomide-O-C7-acid Thalidomide-O-C7-acid
	Thalidomide-O-C7-acid is a compound created through the synthesis of an E3 ligase ligand-linker conjugate. It consists of a cereblon ligand derived from Thalidomide, combined with a linker that is commonly employed in PROTAC technology.
T39838	(S,R,S)-AHPC-C7-amine VH032-C7-amine,(S,R,S)-AHPC-C7-amine
	(S,R,S)-AHPC-C7-amine, also known as VH032-C7-amine, is a chemically synthesized conjugate that functions as an E3 ligase ligand-linker. This compound combines the VH032-based VHL ligand with a specific linker designed for the degradation of estrogen-related receptor α (ERRα) PROTAC.
T39511	Thalidomide-O-C7-NH2 Thalidomide-O-C7-NH2
	Thalidomide-O-C7-NH2 is a synthesized conjugate compound comprising an E3 ligase ligand-linker conjugate. This compound incorporates a cereblon ligand based on Thalidomide and a linker that is commonly employed in PROTAC technology.
T18671	(S,R,S)-AHPC-Me-C7 ester	Others	Others
	(S,R,S)-AHPC-Me-C7 ester is a E3 ligase ligand-linker conjugate used to synthesise BCL-XL PROTAC degraders[1].
T82988	AP-C7
	AP-C7是一种特异性的cGMP依赖性蛋白激酶II (cGKII) 抑制剂，pIC50值为5.0。该化合物对cGKII依赖的阴离子分泌仅表现出弱抑制作用。
T83954	VH 032 amide-alkylC7-acid (S,R,S)-AHPC-amido-C7-acid
	VH 032 amide-alkylC7-acid 是一种用于PROTAC研究与开发的功能化Von-Hippel-Lindau蛋白配体(VHL)，结合了E3连接酶配体和具有末端羧酸的alkylC7连接物，便于与目标蛋白配体偶联。该化合物是为PROTAC研发设计的一系列功能化工具分子之一。
T77954	Thalidomide-5-O-C7-NH2 hydrochloride
	Thalidomide-5-O-C7-NH2 hydrochloride 是 Thalidomide 衍生的 cereblon 配体，能够募集 CRBN 蛋白。该化合物可以利用 linker 结构与靶蛋白配体相连，用于构建 PROTAC 分子，如 THAL-SNS-032。
T77917	Thalidomide-4-O-C7-NH2 hydrochloride
	Thalidomide-4-O-C7-NH2 hydrochloride是一种Thalidomide衍生的CRBN配体，能够招募cereblon蛋白。该化合物能通过linker与目标蛋白配体结合，用于构建PROTAC分子，如THAL-SNS-032。
T19663	Triheptanoin UX 007,IND106011,三庚酸甘油脂,UX007,UX-007,IND 106011,IND-106011	Others	Others
	Triheptanoin (IND 106011) 是合成的中链甘油三酯 (MCT)，由甘油主链上的三个奇数链 7-碳(庚酸)脂肪酸组成，可以用于研究遗传代谢紊乱。
TQ0235	AC710	FLT; PDGFR; c-Kit	Angiogenesis; Tyrosine Kinase/Adaptors
	AC710是一种 PDGFR 抑制剂，能够作用于 FLT3 (Kd:0.6)，CSF1R (Kd:1.57)，KIT (Kd:1)，PDGFRα (Kd:1.3) 和 PDGFRβ (Kd:1.0)。
T15648	KDM5-C70	Histone Demethylase	Chromatin/Epigenetic
	KDM5-C70 是 KDM5-C49 的乙酯衍生物，是一种有效的细胞渗透性泛 KDM5 组蛋白去甲基化酶抑制剂。它在骨髓瘤细胞中具有抗增殖作用，可诱导全基因组 H3K4me3 水平升高。
T11828	LDC7559	Pyroptosis	Apoptosis; Immunology/Inflammation
	LDC7559 通过在晚期阻断中性粒细胞胞外陷阱 (NET)来抑制gasdermin D (GSDMD)。
T3463	NVP-ACC789 ACC-789,ZK202650	VEGFR; PDGFR	Angiogenesis; Tyrosine Kinase/Adaptors
	NVP-ACC789 (ZK202650) 是一种人VEGFR-1，VEGFR-2(鼠VEGFR-2)，VEGFR-3 和 PDGFR-β 的抑制剂，它们的 IC50 值分别为 0.38，0.02 (0.23)，0.18 和 1.4 μM。
T16355	NSC781406	PI3K; mTOR	PI3K/Akt/mTOR signaling
	NSC781406是一种高效PI3K 和mTOR 抑制剂，其PI3Kα的IC50值为2 nM。
T60164	UNC7467	Others	Others
	UNC7467 是一种有效的IP6K 抑制剂，IP6K2、IP6K1 和 IP6K6 的IC50值分别为 4.9、8.9 和1320 nM。UNC7467 可降低肌醇焦磷酸盐的水平，而不会显着干扰其他肌醇磷酸盐的水平。UNC7467 可用于肥胖研究。
T24557	NSC756093 NSC-756093,NSC 756093	Others	Others
	NSC756093 可能抑制 GBP1:PIM1 相互作用。 NSC756093 可用于卵巢癌研究。
T3084	SGC707	Histone Methyltransferase	Chromatin/Epigenetic
	SGC707 是 PRMT3化学探针，是一种有效的、选择性的、细胞活性的 PRMT3 变构抑制剂，IC50值为 31 nM。
T6661	SC75741	Influenza Virus; NF-κB	Microbiology/Virology; NF-κB
	SC75741 是NF-κB 抑制剂，对p65的IC50为 200 nM。它可阻断流感病毒复制。它通过损害NF-κB 亚基 p65 的 DNA 结合，导致细胞因子，趋化因子和促凋亡因子的表达降低，抑制 caspase 活化和阻断 caspase 介导的病毒核糖核蛋白的核输出。
T11372	GC7 Sulfate	Autophagy	Autophagy
	GC7 Sulfate 是 deoxyhypusine synthase(DHS)有效抑制剂。真核翻译起始因子5A2 (eIF5A2)是DHS 已知的底物，因此GC7通过抑制DHS 活性来抑制eIF5A2的激活。
T50125	Compound C749
	Compound C749 是一种有用的有机化合物，可用于生命科学领域的相关研究。其产品编号为 T50125，CAS号为 57-03-4。
T10729	Cdc7-IN-7	CDK	Cell Cycle/Checkpoint
	Cdc7-IN-7 (compound I-E) 是一种有效的 Cdc7 激酶抑制剂。
T2274	SC79 SC 79,2-氨基-6-氯-alpha-氰基-3-(乙氧羰基)-4H-1-苯并吡喃-4-乙酸乙酯	Akt	Cytoskeletal Signaling; PI3K/Akt/mTOR signaling
	SC79 是一个 AKT 激动剂，具有特异性和血脑屏障渗透性。SC79 可以特异性结合 AKT 的 PH 结构域，激活胞质中 AKT，并抑制 AKT 膜转位。SC79 具有神经保护活性。
TP1166	ZINC77292789 Fmoc-Thr[GalNAc(Ac)3-α-D]-OH,Fmoc-Thr(Ac₃AcNH-α-Gal)-OH	Others	Others
	ZINC77292789 (Fmoc-Thr[GalNAc(Ac)3-α-D]-OH) 是制备基于三聚体 MUC1 免疫显性基序抗原的候选抗癌疫苗的起始材料，可制备含有 βGalNAc-Thr 作为 Tn 抗原异构体的合成 MUC1 糖肽，可诱导针对肿瘤细胞的抗体产生。
T23867	Cdc7-IN-7c Cdc7 inhibitor-7c,Cdc7 inhibitor 7c,Cdc7 IN 7c	CDK	Cell Cycle/Checkpoint
	Cdc7-IN-7c (Cdc7 inhibitor-7c) 具有抗肿瘤活性，对肝癌，肺癌，肾癌，脑癌，宫颈癌有抑制作用。
T10656	trans-C75 (±)-C75,反-4-羧基-5-辛基-3-甲基-丁内酯	Others; Fatty Acid Synthase	Metabolism; Others
	trans-C75 ((±)-C75) 是一种 C75 的对映异构体。其中 C75 是一种脂肪酸合成酶 (FASN) 的抑制剂。
T3169	KC7F2	HIF/HIF Prolyl-Hydroxylase; HIF	Angiogenesis; Chromatin/Epigenetic; Metabolism
	KC7F2 是缺氧诱导因子HIF-1通道抑制剂，在 LN229-HRE-AP 细胞中的IC50=20 μM，可用作抗癌试剂。
T10727	Cdc7-IN-5	CDK	Cell Cycle/Checkpoint
	Cdc7-IN-5 是一种有效的 Cdc7 激酶抑制剂。Cdc7 是一种丝氨酸苏氨酸蛋白激酶酶，在细胞周期中对 DNA 复制的启动至关重要。
T10657	C75 C-75	Fatty Acid Synthase	Metabolism
	C75 是一种合成脂肪酸合酶 (FASN) 抑制剂，可抑制前列腺癌细胞 PC3 (IC50: 35 μM)。
T62921	EBNA1-IN-SC7
	EBNA1-IN-SC7 (compound SC7) 是一种 Epstein-Barr nuclear antigen 1 (EBNA1) 的选择性抑制剂，能够干扰 EBNA1-DNA 结合活性 (IC50: 23 μM)。EBNA1-IN-SC7 能够用于研究 EBV (Epstein-Barr virus) 相关癌症。
T75168	Homo-BacPROTAC7
	Homo-BacPROTAC7 是一个 ClpC1NTDBacPROTAC 降解剂，可以靶向 ClpC2。Homo-BacPROTAC7 能有效杀死 M. tuberculosis。
T61223	Cdc7-IN-19
	Cdc7-IN-19 (compound 1-1) 是一种有效的CDC7抑制剂，对 Cdc7/DBF4 酶的IC50为 1.49 nM。
T71762	TLSC702
	TLSC702 is a novel Inhibitor of Human Glyoxalase I, Inducing Apoptosis in Tumor Cells.
T61289	Cdc7-IN-14
	Cdc7-IN-14 (compound 82) is a highly potent inhibitor of CDC7, demonstrating an IC50 value of less than 1 nM. This compound, Cdc7-IN-14, exhibits promising potential for cancer research [1].
T74514	HD-TAC7	PROTACs	PROTAC
	HD-TAC7 是一种有效的 PROTACHDAC 降解剂，对 HDAC1、HDAC2 和 HDAC3的 IC50分别为 3.6 μM、4.2 μM 和 1.1 μM。HD-TAC7 可降低 RAW 264.7 巨噬细胞NF-κBp65 表达。HD-TAC7 可用于哮喘和慢性阻塞性肺病（COPD）等炎症性疾病的研究。
T80408	Bac7(1-35)
	Bac7(1-35)是一种选择性针对革兰氏阴性菌的脯氨酸富集型抗菌肽，在经过膜易位作用后在细胞内发挥效能。
T78271	Anti-Mouse TCR gamma/delta Antibody (UC7-13D5)
	Anti-Mouse TCR gamma/delta Antibody为针对小鼠TCR gamma/delta的IgG类免疫抑制抗体，其宿主为亚美尼亚仓鼠。
T79616	UNC7096	Histone Methyltransferase	Chromatin/Epigenetic
	UNC7096为一种选择性NSD2-PWWP1抑制剂，其Kd为46 nM，拥有潜在治疗NSD2相关疾病的能力。
T70151	MeTC7
	MeTC7 is a VDR antagonist, which can be synthesized from 7-dehydrocholesterol (6) in two steps, inhibits VDR selectively, suppresses the viability of cancer cell-lines, and reduces the growth of the spontaneous transgenic TH-MYCN neuroblastoma and xenografts in vivo.
T24135	HEC72702 HEC-72702,HEC 72702
	HEC72702 is a novel Hepatitis B virus capsid inhibitor, based on clinical candidate GLS4. HEC72702 was found to display no induction of the CYP1A2, CYP3A4, or CYP2B6 enzyme at the high concentration of 10 μM.
T10228	AC710 Mesylate	PDGFR	Angiogenesis; Tyrosine Kinase/Adaptors
	AC710 Mesylate is a potent PDGFR inhibitor (Kds: 0.6, 1.57, 1, 1.3, 1.0 nM for FLT3, CSF1R, KIT, PDGFRα and PDGFRβ).
T16354	NSC745885	Others	Others
	NSC745885 is an effective down-regulator of EZH2 via proteasome-mediated degradation. NSC745885 is also an effective anti-tumor agent that displays selective toxicity against multiple cancer cell lines but not normal cells. NSC745885 offers possibilities
T29542	AC708 AC 708,AC-708
	AC708 is a small molecule CSF1R inhibitor that effectively inhibits CSF1R phosphorylation mediated by CSF-1 (IC50 = 26 nM) and IL-34 (IC50 = 33 nM). It also inhibited the activity of growth factor-dependent cells cultured in CSF-1 (IC50 = 38 nM) or IL-34
T61224	Cdc7-IN-8
	Cdc7-IN-8, a potent inhibitor, targets Cdc7, a serine/threonine kinase responsible for activating MCM promotion through phosphorylation of the microchromosome maintenance protein (MCM protein). MCM protein, an essential component of DNA replication initiation, plays a crucial role. Cdc7-IN-8 holds promise in cancer disease research (WO2021032170A1, compound 1-1/1-2) [1].
T61435	(S)-Cdc7-IN-18
	(S)-Cdc7-IN-18, a potent CDC7 inhibitor, effectively impedes the overactivation of MCM2, a crucial tumor cell marker, induced by huCdc7 overexpression. Consequently, it inhibits the aberrant proliferation of tumor cells. This compound, exhibits promise for cancer disease research [1].
T78423	ARC7
	ARC7是一种用于探测S. coelicolor次生代谢的化合物，同时也被作为研究次生代谢和链霉菌生命周期的实用工具。
T10726	Cdc7-IN-4	Others	Others
	Cdc7-IN-4 is a potent inhibitor of Cdc7 kinase.
T24682	PTC725 PTC-725,PTC 725
	PTC725 is a selective HCV 1b replicons inhibitor. It has been shown to target the nonstructural protein 4B.
T61288	Cdc7-IN-13
	Cdc7-IN-13 (compound 84) is a highly potent CDC7 inhibitor, exhibiting an IC50 value of <1 nM. This compound holds promise for cancer research [1].

化合物

Pomalidomide-C7-NH2 hydrochloride

Cat.No: T40004

Target: Others

Pomalidomide-C7-COOH

Cat.No: T39701

Synonym: Pomalidomide-C7-COOH

Thalidomide-O-C7-acid

Cat.No: T39645

Synonym: Thalidomide-O-C7-acid

(S,R,S)-AHPC-C7-amine

Cat.No: T39838

Synonym: VH032-C7-amine,(S,R,S)-AHPC-C7-amine

Thalidomide-O-C7-NH2

Cat.No: T39511

Synonym: Thalidomide-O-C7-NH2

(S,R,S)-AHPC-Me-C7 ester

Cat.No: T18671

Target: Others

Cat.No: T82988

VH 032 amide-alkylC7-acid

Cat.No: T83954

Synonym: (S,R,S)-AHPC-amido-C7-acid

Thalidomide-5-O-C7-NH2 hydrochloride

Cat.No: T77954

Thalidomide-4-O-C7-NH2 hydrochloride

Cat.No: T77917

Cat.No: T19663

Synonym: UX 007,IND106011,三庚酸甘油脂,UX007,UX-007,IND 106011,IND-106011

Target: Others

Cat.No: TQ0235

Target: FLT, PDGFR, c-Kit

Cat.No: T15648

Target: Histone Demethylase

Cat.No: T11828

Target: Pyroptosis

Cat.No: T3463

Synonym: ACC-789,ZK202650

Target: VEGFR, PDGFR

Cat.No: T16355

Target: PI3K, mTOR

Cat.No: T60164

Target: Others

Cat.No: T24557

Synonym: NSC-756093,NSC 756093

Target: Others

Cat.No: T3084

Target: Histone Methyltransferase

Cat.No: T6661

Target: Influenza Virus, NF-κB

Cat.No: T11372

Target: Autophagy

Cat.No: T50125

Cat.No: T10729

Target: CDK

Cat.No: T2274

Synonym: SC 79,2-氨基-6-氯-alpha-氰基-3-(乙氧羰基)-4H-1-苯并吡喃-4-乙酸乙酯

Target: Akt

Cat.No: TP1166

Synonym: Fmoc-Thr[GalNAc(Ac)3-α-D]-OH,Fmoc-Thr(Ac₃AcNH-α-Gal)-OH

Target: Others

Cat.No: T23867

Synonym: Cdc7 inhibitor-7c,Cdc7 inhibitor 7c,Cdc7 IN 7c

Target: CDK

Cat.No: T10656

Synonym: (±)-C75,反-4-羧基-5-辛基-3-甲基-丁内酯

Target: Others, Fatty Acid Synthase

Cat.No: T3169

Target: HIF/HIF Prolyl-Hydroxylase, HIF

Cat.No: T10727

Target: CDK

Cat.No: T10657

Synonym: C-75

Target: Fatty Acid Synthase

Cat.No: T62921

Homo-BacPROTAC7

Cat.No: T75168

Cat.No: T61223

Cat.No: T71762

Cat.No: T61289

Cat.No: T74514

Target: PROTACs

Cat.No: T80408

Anti-Mouse TCR gamma/delta Antibody (UC7-13D5)

Cat.No: T78271

Cat.No: T79616

Target: Histone Methyltransferase

Cat.No: T70151

Cat.No: T24135

Synonym: HEC-72702,HEC 72702

Cat.No: T10228

Target: PDGFR

Cat.No: T16354

Target: Others

Cat.No: T29542

Synonym: AC 708,AC-708

Cat.No: T61224

Cat.No: T61435

Cat.No: T78423

Cat.No: T10726

Target: Others

Cat.No: T24682

Synonym: PTC-725,PTC 725

Cat.No: T61288

Species：

Expression System：

Tag：

Cat. No.	Product Name	Species	Expression System
TMPY-02892	Complement C7 Protein, Human, Recombinant (His) Complement C7,complement component 7	Human	HEK293 Cells
	Complement C7 Protein, Human, Recombinant (His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 92.6 kDa and the accession number is P10643.
TMPY-03012	Complement C7 Protein, Human, Recombinant (hFc) complement component 7,Complement C7	Human	HEK293 Cells
	Complement C7 Protein, Human, Recombinant (hFc) is expressed in HEK293 mammalian cells with hFc tag. The predicted molecular weight is 118 kDa and the accession number is P10643.
TMPY-02970	CXCL10 Protein, Human, Recombinant IFI10,IP-10,chemokine (C-X-C motif) ligand 10,gIP-10,crg-2,<...	Human	E. coli
	CXCL10 Protein, Human, Recombinant is expressed in E. coli expression system. The predicted molecular weight is 8.8 kDa and the accession number is P02778.
TMPK-01269	CXCL10 Protein, Cynomolgus, Recombinant (His) IFI10,gIP-10,CXCL10,IP-10,SCYB10,C-X-C motif chemokine 10,cr...	Cynomolgus	E. coli
	C-X-C motif ligand 10 (CXCL10), or interferon-inducible protein-10, is a small chemokine belonging to the CXC chemokine family. Its members are responsible for leukocyte trafficking and act on tissue cells, like endothelial and vascular smooth muscle cells. CXCL10 is secreted by leukocytes and tissue cells and functions as a chemoattractant, mainly for lymphocytes.
TMPH-03750	SLC7A11 Protein, Human, Recombinant (His)	Human	E. coli
	Sodium-independent, high-affinity exchange of anionic amino acids with high specificity for anionic form of cystine and glutamate.
TMPY-04118	Livin/BIRC7 Protein, Human, Recombinant (His) MLIAP,baculoviral IAP repeat containing 7,RNF50,KIAP,ML-IAP,...	Human	E. coli
	BIRC7, a new member of inhibitor of the apoptosis protein family, is expressed in fetal tissues and most solid tumors in humans. BIRC7/livin expression is a novel prognostic marker in adult acute leukemia. Livin/BIRC7 is a member of the inhibitors of apoptosis proteins family, which are involved in tumor development through the inhibition of caspases. Livin/BIRC7 is specifically over-expressed in ACC, suggesting that it might be involved in adrenocortical tumorigenesis and represent a new molecu...
TMPY-02217	HSC70 Protein, Human, Recombinant (His) HSP73,HSC54,HSP71,NIP71,LAP-1,HEL-33,HSPA10,HSC71,L...	Human	E. coli
	HSPA8, also known as HSC70, is a member of the heat shock protein family due to homology with other heat shock proteins. The heat shock protein 70 family is comprised of both heat-inducible and constitutively expressed members. The latter are called heat-shock cognate proteins. HSPA8 belongs to the heat-shock cognate subgroup. Members of the human heat-shock protein multigene family have several highly conserved proteins with structural and functional properties in common but vary in the extent ...
TMPK-01049	CLEC7A Protein, Mouse, Recombinant (hFc) CLECSF12,DC-associated C-type lectin 1,Dectin-1,Beta-glucan ...	Mouse	HEK293 Cells
	Dendritic cell-associated C-type lectin-1 (Dectin-1), also known as β-glucan receptor is an emerging pattern recognition receptor (PRR) which belongs to the family of C-type lectin receptor (CLR). Dectin-1 signaling axis has been suggested to be targeted as an effective therapeutic strategy for cancers. Dectin-1 has also been elucidated ascetically in the heart, respiratory, intestinal, neurological and developmental disorders.
TMPH-01475	HDAC7 Protein, Human, Recombinant (His)	Human	E. coli
	N/A. HDAC7 Protein, Human, Recombinant (His) is expressed in E. coli expression system with N-6xHis tag. The predicted molecular weight is 26 kDa and the accession number is Q8WUI4 (BC064840).
TMPH-01604	SLC7A5 Protein, Human, Recombinant (His & Myc & SUMO)	Human	E. coli
	SLC7A5 Protein, Human, Recombinant (His & Myc & SUMO) is expressed in E. coli expression system with N-10xHis-SUMO and C-Myc tag. The predicted molecular weight is 19.7 kDa and the accession number is Q01650.
TMPY-04061	HIV-2 (subtype CRF01_AB, strain 07JP_NMC716_clone_01) gp36 Protein (His & MBP) GP36	HIV	E. coli
	HIV-2 (subtype CRF01_AB, strain 07JP_NMC716_clone_01) gp36 Protein (His & MBP) is expressed in E. coli expression system with His and MBP tag. The predicted molecular weight is 58.8 kDa and the accession number is L8B302.
TMPH-02528	SLC7A10 Protein, Mouse, Recombinant (His & SUMOstar)	Mouse	P. pastoris (Yeast)
	Sodium-independent, high affinity transport of small neutral D- and L-amino acids and amino acid-related compounds. May play a role in the modulation of glutamatergic transmission through mobilization of D-serine at the glutamatergic synapse. SLC7A10 Protein, Mouse, Recombinant (His & SUMOstar) is expressed in yeast with N-His tag. The predicted molecular weight is 22.5 kDa and the accession number is P63115.
TMPH-00218	DHCR7 Protein, Bovine, Recombinant (His) DHCR7,7-dehydrocholesterol reductase,Sterol Delta(7)-reducta...	Bovine	E. coli
	7-dehydrocholesterol reductase of the cholesterol biosynthetic pathway reducing the C7-C8 double bond of cholesta-5,7-dien-3beta-ol (7-dehydrocholesterol/7-DHC) and cholesta-5,7,24-trien-3beta-ol, two intermediates in that pathway. DHCR7 Protein, Bovine, Recombinant (His) is expressed in E. coli expression system with N-10xHis tag. The predicted molecular weight is 55.8 kDa and the accession number is Q5E9J5.

重组蛋白

Complement C7 Protein, Human, Recombinant (His)

Cat.No: TMPY-02892

Species: Human

Expression System: HEK293 Cells

Complement C7 Protein, Human, Recombinant (hFc)

Cat.No: TMPY-03012

Species: Human

Expression System: HEK293 Cells

CXCL10 Protein, Human, Recombinant

Cat.No: TMPY-02970

Species: Human

Expression System: E. coli

CXCL10 Protein, Cynomolgus, Recombinant (His)

Cat.No: TMPK-01269

Species: Cynomolgus

Expression System: E. coli

SLC7A11 Protein, Human, Recombinant (His)

Cat.No: TMPH-03750

Species: Human

Expression System: E. coli

Livin/BIRC7 Protein, Human, Recombinant (His)

Cat.No: TMPY-04118

Species: Human

Expression System: E. coli

HSC70 Protein, Human, Recombinant (His)

Cat.No: TMPY-02217

Species: Human

Expression System: E. coli

CLEC7A Protein, Mouse, Recombinant (hFc)

Cat.No: TMPK-01049

Species: Mouse

Expression System: HEK293 Cells

HDAC7 Protein, Human, Recombinant (His)

Cat.No: TMPH-01475

Species: Human

Expression System: E. coli

SLC7A5 Protein, Human, Recombinant (His & Myc & SUMO)

Cat.No: TMPH-01604

Species: Human

Expression System: E. coli

HIV-2 (subtype CRF01_AB, strain 07JP_NMC716_clone_01) gp36 Protein (His & MBP)

Cat.No: TMPY-04061

Species: HIV

Expression System: E. coli

SLC7A10 Protein, Mouse, Recombinant (His & SUMOstar)

Cat.No: TMPH-02528

Species: Mouse

Expression System: P. pastoris (Yeast)

DHCR7 Protein, Bovine, Recombinant (His)

Cat.No: TMPH-00218

Species: Bovine

Expression System: E. coli

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