Penicillin-Streptomycin (10,000 U/mL)
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Penicillin-Streptomycin (10,000 U/mL)
Penicillin-Streptomycin (10,000 U/mL)
Penicillin-Streptomycin (10,000 U/mL)
인용 및 참조 문헌 (43)
Gibco™

Penicillin-Streptomycin (10,000 U/mL)

본 제품은 그램 양성균과 그램 음성균에 효과적인 활성을 보이는 penicillin와 streptomycin 항생제가 복합되어 있어 세포 배양 시 세균 오염을 예방하기자세히 알아보기
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카탈로그 번호수량
15140148
15140-148으로도 사용됨
20 mL
15140122
15140-122으로도 사용됨
100 mL
15140163
15140-163으로도 사용됨
20 x 100 mL
카탈로그 번호 15140148
15140-148으로도 사용됨
제품 가격(KRW)
28,000
Online offer
Ends: 31-Mar-2026
31,000
할인액 3,000 (10%)
Each
카트에 추가하기
수량:
20 mL
제품 가격(KRW)
28,000
Online offer
Ends: 31-Mar-2026
31,000
할인액 3,000 (10%)
Each
카트에 추가하기
본 제품은 그램 양성균과 그램 음성균에 효과적인 활성을 보이는 penicillin와 streptomycin 항생제가 복합되어 있어 세포 배양 시 세균 오염을 예방하기 위하여 사용할 수 있습니다. Penicillin은 원래 진균인 Penicillium에서 정제된 물질로 세균 세포벽 전환을 직접적으로 저해하고 세포벽을 변형시키는 효소 분비를 유도하는 간접 억제 작용을 합니다. Streptomycin는 원래 Streptomyces griseus에서 정제된 물질입니다. Streptomycin은 세균 리소좀 30S에 결합해 단백질 합성을 억제하고 감수성 높은 세균의 사멸을 유도합니다. 라이프 테크놀로지스는 세포 배양 어플리케이션에 사용하는 다양한 항생∙항진균제 를 제공합니다.

이 솔루션에는 penicillin 10000 단위와 streptomycin 10000 μg/ml가 함유되어 있습니다.

Life Technologies offers a wide range of antibiotics and antimycotics in both powder and liquid formats. See the complete list, or find products for:
• Contamination control
• Eukaryotic and bacterial selection

See recommended working concentrations for selection antibiotics.

Learn more about the use of antibiotics and antimycotics in cell culture and review guidelines for decontaminating cultures.

본 제품은 냉장/냉동제품으로 반송된 제품은 전량 폐기 처리 되오니 주문 전 상세 내용 다시 한번 확인 부탁드립니다.
For Research Use Only. Not for use in diagnostic procedures.
사양
농도100 X
용도(애플리케이션)Prevention of Cell Culture Contamination
수량20 mL
유통 기한12 Months
배송 조건Dry Ice
형태Liquid
제품 유형Antibiotic
멸균Sterile-filtered
Sterilization MethodSterile-filtered
Unit SizeEach
구성 및 보관
Storage conditions: -5 to -20°C
Shipping conditions: Frozen
Shelf life: 12 months from date of manufacture

자주 묻는 질문(FAQ)

My Penicillin-Streptomycin solution is not colorless. Is this normal?

Yes, this is normal and will not affect the potency or application of the product. This solution is typically colorless. However, it can have a pink to yellow color tint. The coloring is a carry-over from the manufacturing process of Streptomycin - the genus that Steptomycin is isolated from (Actinomycetes Streptomyces griseus) is responsible for a wide variety of pigments.

Find additional tips, troubleshooting help, and resources within our Cell Culture Support Center.

How can I decontaminate my cultures?

When an irreplaceable culture becomes contaminated, researchers may attempt to eliminate or control the contamination.

1. Determine if the contamination is bacteria, fungus, mycoplasma, or yeast. Read more here to view characteristics of each contaminant.
2. Isolate the contaminated culture from other cell lines.
3. Clean incubators and laminar flow hoods with a laboratory disinfectant, and check HEPA filters.
4. Antibiotics and antimycotics at high concentrations can be toxic to some cell lines. Therefore, perform a dose-response test to determine the level at which an antibiotic or antimycotic becomes toxic. This is particularly important when using an antimycotic such as Gibco Fungizone reagent or an antibiotic such as tylosin.

The following is a suggested procedure for determining toxicity levels and decontaminating cultures:

1. Dissociate, count, and dilute the cells in antibiotic-free media. Dilute the cells to the concentration used for regular cell passage.
2. Dispense the cell suspension into a multiwell culture plate or several small flasks. Add the antibiotic of choice to each well in a range of concentrations. For example, we suggest the following concentrations for Gibco Fungizone reagent: 0.25, 0.50, 1.0, 2.0, 4.0, and 8.0 µg/mL.
3. Observe the cells daily for signs of toxicity such as sloughing, appearance of vacuoles, decrease in confluency, and rounding.
4. When the toxic antibiotic level has been determined, culture the cells for two to three passages using the antibiotic at a concentration one- to two-fold lower than the toxic concentration.
5. Culture the cells for one passage in antibiotic-free media.
6. Repeat step 4.
7. Culture the cells in antibiotic-free medium for four to six passages to determine if the contamination has been eliminated.

Find additional tips, troubleshooting help, and resources within our Cell Culture Support Center.

What antibiotics do you offer to help control or eliminate cell culture contamination?

Please view the following page to browse the cell culture antibiotics we offer (https://www.thermofisher.com/us/en/home/life-science/cell-culture/mammalian-cell-culture/antibiotics.html).

Find additional tips, troubleshooting help, and resources within our Cell Culture Support Center.

인용 및 참조 문헌 (43)

인용 및 참조 문헌
Abstract
Identification of a novel redox-sensitive gene, Id3, which mediates angiotensin II-induced cell growth.
Authors:Mueller Cornelius; Baudler Stephanie; Welzel Hilke; Böhm Michael; Nickenig Georg;
Journal:Circulation
PubMed ID:12021231
BACKGROUND: Reactive oxygen species, such as superoxide (O(2)(-)), are involved in the abnormal growth of various cell types. Angiotensin II (Ang II) is one of the most potent inducers of oxidative stress in the vasculature. The molecular events involved in Ang II-induced proliferation of vascular smooth muscle cells (VSMCs) are ... More
Functional interaction of caveolin-1 with Bruton's tyrosine kinase and Bmx.
Authors: Vargas Leonardo; Nore Beston F; Berglof Anna; Heinonen Juhana E; Mattsson Pekka T; Smith C I Edvard; Mohamed Abdalla J;
Journal:J Biol Chem
PubMed ID:11751885
'Bruton''s tyrosine kinase (Btk), a member of the Tec family of protein-tyrosine kinases, has been shown to be crucial for B cell development, differentiation, and signaling. Mutations in the Btk gene lead to X-linked agammaglobulinemia in humans and X-linked immunodeficiency in mice. Using a co-transfection approach, we present evidence here ... More
Repression of activator protein-1-mediated transcriptional activation by the Notch-1 intracellular domain.
Authors: Chu Jianlin; Jeffries Shawn; Norton Jason E; Capobianco Anthony J; Bresnick Emery H;
Journal:J Biol Chem
PubMed ID:11739397
'Developmental decisions that control cell fate are commonly regulated by the Notch signaling pathway. Activation of transmembrane Notch receptors results in proteolytic liberation of the intracellular domain of Notch, which translocates into the nucleus, binds a repressor (C promoter binding factor 1/RBP-Jkappa, Su(H), and Lag-1 (CSL)), and induces target genes. ... More
A differential role for the mitogen-activated protein kinases in lipopolysaccharide signaling: the MEK/ERK pathway is not essential for nitric oxide and interleukin 1beta production.
Authors: Watters Jyoti J; Sommer Julie A; Pfeiffer Zachary A; Prabhu Usha; Guerra Alma N; Bertics Paul J;
Journal:J Biol Chem
PubMed ID:11786532
'Endotoxin (lipopolysaccharide, LPS) is a component of the outer membrane of Gram-negative bacteria and promotes the activation of macrophages and microglia. Although these cells are highly LPS-responsive, they serve unique tissue-specific functions and exhibit different LPS sensitivities. Accordingly, it was of interest to evaluate whether these biological differences reside in ... More
Cholesteryl ester is transported from caveolae to internal membranes as part of a caveolin-annexin II lipid-protein complex.
Authors: Uittenbogaard Annette; Everson William V; Matveev Sergey V; Smart Eric J;
Journal:J Biol Chem
PubMed ID:11733519
'We previously demonstrated that in Chinese hamster ovary cells scavenger receptor, class B, type I-dependent selective cholesteryl ester uptake occurs in caveolae. In the present study we hypothesized that cholesteryl ester is transported from caveolae through the cytosol to an internal membrane by a caveolin chaperone complex similar to the ... More
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