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Gibco™
MCDB 131 Medium, no glutamine
MCDB 131 Medium was originally developed by Knedler and Ham as reduced serum-supplemented medium for the culture of human microvascular자세히 알아보기
| 카탈로그 번호 | 수량 |
|---|---|
| 10372019 | 500 mL |
카탈로그 번호 10372019
제품 가격(KRW)
111,000
Each
재고 준비 예상일 25-Jul-2025
수량:
500 mL
제품 가격(KRW)
111,000
Each
MCDB 131 Medium was originally developed by Knedler and Ham as reduced serum-supplemented medium for the culture of human microvascular endothelial cells (HMVEC). MCDB 131 Medium is also used with other cell types, including human omental microvascular cells, hepatocytes, myocytes, and smooth muscle cells.
This MCDB 131 Medium is manufactured as follows:
The complete formulation is available.
Using MCDB 131
MCDB 131 Medium contains many components not found in traditional basal media, such as trace elements, putrescine, adenine, thymidine, and higher levels of some amino acids and vitamins. These additions allow the medium to be supplemented with very low levels of serum or defined components. MCDB 131 Medium contains no proteins or growth factors, and is often supplemented with EGF, hydrocortisone, glutamine, and low levels of Fetal Bovine Serum (FBS). The FBS concentration must be optimized for each cell type. MCDB 131 Medium uses a sodium bicarbonate buffer system (1.176 g/L), and therefore requires a 5–10% CO2 environment to maintain physiological pH.
Dual-site cGMP manufacturing
For supply chain continuity, we manufacture MCDB 131 at two separate facilities, located in Grand Island, NY and Scotland, UK. Both sites are compliant with cGMP-manufacturing requirements, are certified to ISO 13485, and are registered with the FDA as medical device manufacturers.
This MCDB 131 Medium is manufactured as follows:
| With | Without |
| • Phenol Red | • L-glutamine |
| • Sodium pyruvate | • HEPES |
The complete formulation is available.
Using MCDB 131
MCDB 131 Medium contains many components not found in traditional basal media, such as trace elements, putrescine, adenine, thymidine, and higher levels of some amino acids and vitamins. These additions allow the medium to be supplemented with very low levels of serum or defined components. MCDB 131 Medium contains no proteins or growth factors, and is often supplemented with EGF, hydrocortisone, glutamine, and low levels of Fetal Bovine Serum (FBS). The FBS concentration must be optimized for each cell type. MCDB 131 Medium uses a sodium bicarbonate buffer system (1.176 g/L), and therefore requires a 5–10% CO2 environment to maintain physiological pH.
Dual-site cGMP manufacturing
For supply chain continuity, we manufacture MCDB 131 at two separate facilities, located in Grand Island, NY and Scotland, UK. Both sites are compliant with cGMP-manufacturing requirements, are certified to ISO 13485, and are registered with the FDA as medical device manufacturers.
For Research Use Only. Not for use in diagnostic procedures.
사양
세포 유형Human Microvascular Endothelial Cells (HMVEC), Human Omental Microvascular Cells, Hepatocytes, Myocytes, Smooth Muscle Cells
농도1 X
제품라인Gibco™
제품 유형MCDB 131 Medium
수량500 mL
유통 기한12 Months From Date of Manufacture
배송 조건Room Temperature
Culture TypeMammalian Cell Culture
형태Liquid
멸균Sterile-filtered
첨가제 포함Low Glucose, Phenol Red, Sodium Pyruvate
첨가제 없음No Glutamine, No HEPES
Unit SizeEach
구성 및 보관
Storage conditions: 2–8°C (protect from light)
Shelf life: 12 months from date of manufacture
Shelf life: 12 months from date of manufacture
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Certificates | 증명서
Lot 번호 또는 부분 Lot 번호로 검색하십시오.
Lot 번호Certificate TypeDateCatalog Number(s)
3138588Certificate of Analysis2025년 6월 15일10372019
3090825Certificate of Analysis2025년 5월 25일10372019
3124501Certificate of Analysis2025년 5월 03일10372019
3137152Certificate of Analysis2025년 3월 30일10372019
3062407Certificate of Analysis2025년 3월 16일10372019
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SDS인용 및 참조 문헌 (1)
Search citations by name, author, journal title or abstract text
인용 및 참조 문헌
Abstract
Directed differentiation of pancreatic δ cells from human pluripotent stem cells.
Journal:Nature communications
PubMed ID:39068220
Dysfunction of pancreatic δ cells contributes to the etiology of diabetes. Despite their important role, human δ cells are scarce, limiting physiological studies and drug discovery targeting δ cells. To date, no directed δ-cell differentiation method has been established. Here, we demonstrate that fibroblast growth factor (FGF) 7 promotes pancreatic
1 total citations