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370 Results for "

Hela

" in MedChemExpress (MCE) Product Catalog:

Products (370)

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PEI Transfection Reagent

71 Publications Verification

Cat. No.: HY-K2014

MCE PEI Transfection Reagent is designed based on 25 kDa PEI. It has high-efficiency, low-toxicity, strong-stability, and is suitable for many cell types, such as HEK-293、HEK-293T、CHO-K1、COS-1、COS-7、NIH/3T3、Sf9、HepG2 and HeLa et, even some hard-to-transfect cells. It can also be applied to large-scale recombinant protein expression and virus production. The 1 mL is defined as the base specification. All larger sizes correspond to incremental volumes of this base.

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Niclosamide

47 Cited Publications

Cat. No.: HY-B0497

CAS No.: 50-65-7

Synonyms: BAY2353

Target:

Environmental Pollutants Antibiotic Parasite STAT

Research Areas:

Infection Cancer

Niclosamide (BAY2353) is an orally active antihelminthic agent used in parasitic infection research . Niclosamide is a STAT3 inhibitor with an IC₅₀ of 0.25 μM in HeLa cells . Niclosamide has biological activities against cancer, inhibits DNA replication in Vero E6 cells .

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Niclosamide olamine

47 Cited Publications

Cat. No.: HY-B0497C

CAS No.: 1420-04-8

Synonyms: BAY2353 olamine

Target:

Environmental Pollutants Antibiotic STAT Parasite

Research Areas:

Infection Cancer

Niclosamide (BAY2353) olamine is an orally active antihelminthic agent used in parasitic infection research . Niclosamide olamin is a STAT3 inhibitor with an IC₅₀ of 0.25 μM in HeLa cells . Niclosamide olamin has biological activities against cancer, and inhibits DNA replication in Vero E6 cells .

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Belinostat

41 Cited Publications

Cat. No.: HY-10225

CAS No.: 866323-14-0

Purity: 99.95%

Synonyms: PXD101; PX105684; PDX 101

Target:

HDAC Autophagy

Research Areas:

Cancer

Belinostat (PXD101; PX105684) is a potent HDAC inhibitor with an IC₅₀ of 27 nM in HeLa cell extracts.

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STO-609

39 Cited Publications

Cat. No.: HY-19805

CAS No.: 52029-86-4

Target:

CaMK AMPK Autophagy

Research Areas:

Metabolic Disease

STO-609 is a selective and cell-permeable inhibitor of the Ca ²⁺/calmodulin-dependent protein kinase kinase (CaM-KK), with K_i values of 80 and 15 ng/mL for recombinant CaM-KKα and CaM-KKβ, respectively. STO-609 inhibits AMP-activated protein kinase kinase (AMPKK) activity in HeLa cell lysates with an IC₅₀ ~0.02 g/ml.

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