UltraPure™ 0.5M EDTA, pH 8.0
UltraPure™ 0.5M EDTA, pH 8.0
Invitrogen™

UltraPure™ 0.5M EDTA, pH 8.0

UltraPure™ 0.5 M EDTA, pH 8.0 is an aqueous solution prepared by dissolving Na2EDTA•2H2O in distilled, deionized water and adjusting深入閱讀
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產品號碼Quantity
155750204 x 100 mL
產品號碼 15575020
價格 (TWD)
2,350.00
線上優惠
Ends: 31-Dec-2025
3,130.00
您節省 780.00 (25%)
Each
新增至購物車
Quantity:
4 x 100 mL
Request bulk or custom format
價格 (TWD)
2,350.00
線上優惠
Ends: 31-Dec-2025
3,130.00
您節省 780.00 (25%)
Each
新增至購物車
UltraPure™ 0.5 M EDTA, pH 8.0 is an aqueous solution prepared by dissolving Na2EDTA•2H2O in distilled, deionized water and adjusting the pH to 8.0 with sodium hydroxide. This sterile-filtered solution is suitable for biochemistry or molecular biology applications requiring a chelator of divalent metal ions.
For Research Use Only. Not for use in diagnostic procedures.
規格
Chemical Name or MaterialEDTA
Concentration0.5 M
For Use With (Application)Chromatin Biology, Nucleic Acid Gel Electrophoresis, Blotting
FormLiquid
Product LineUltraPure
Product TypeEDTA
PurityMolecular Biology Grade
Quantity4 x 100 mL
Shipping ConditionRoom Temperature
pHpH 8.0
Unit SizeEach
內容物與存放
Contents: 4 bottles (100 mL each) of UltraPure™ 0.5M EDTA, pH 8.0. Store at room temperature.

常見問答集 (常見問題)

I received a shipment of UltraPure 0.5M EDTA, pH 8.0 (Cat. No. 15575020), but it was stored below 15-30 degrees C over the weekend. Can you confirm this product will still be stable?

We do not have specific data for temperatures below 15 degrees C for UltraPure 0.5M EDTA, pH 8.0 (Cat. No. 15575020). However, as long as the product was not frozen, the performance should not be affected.

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

What is the difference between EDTA and EGTA?

EDTA binds Mg2+ and Ca2+, while EGTA specifically binds to Ca2+. The use of EGTA may be favored in case where subsequent treatment with Mg2+ dependent enzymes is planned.

How does EDTA work?

EDTA reversibly binds Mg2+, Ca2+ as well as other divalent cations, thus inhibiting enyzmes that require these cations for activity.

引用資料與參考文獻 (7)

引用資料與參考文獻
Abstract
A comprehensive protocol for efficient differentiation of human NPCs into electrically competent neurons.
Authors:Romito E,Battistella I,Plakhova V,Paplekaj A,Forastieri C,Toffolo E,Musio C,Conti L,Battaglioli E,Rusconi F
Journal:Journal of neuroscience methods
PubMed ID:39053772
Nondestructive sampling of human skeletal remains yields ancient nuclear and mitochondrial DNA.
Authors:Bolnick DA, Bonine HM, Mata-Míguez J, Kemp BM, Snow MH, LeBlanc SA
Journal:Am J Phys Anthropol
PubMed ID:22183740
'Museum curators and living communities are sometimes reluctant to permit ancient DNA (aDNA) studies of human skeletal remains because the extraction of aDNA usually requires the destruction of at least some skeletal material. Whether these views stem from a desire to conserve precious materials or an objection to destroying ancestral ... More
Digital gene expression by tag sequencing on the illumina genome analyzer.
Authors:Morrissy S, Zhao Y, Delaney A, Asano J, Dhalla N, Li I, McDonald H, Pandoh P, Prabhu AL, Tam A, Hirst M, Marra M
Journal:Curr Protoc Hum Genet
PubMed ID:20373513
'This unit provides a protocol for performing digital gene expression profiling on the Illumina Genome Analyzer sequencing platform. Tag sequencing (Tag-seq) is an implementation of the LongSAGE protocol on the Illumina sequencing platform that increases utility while reducing both the cost and time required to generate gene expression profiles. The ... More
DNA extraction from aged skeletal samples for STR typing by capillary electrophoresis.
Authors:Huel R, Amory S, Bilic A, Vidovic S, Jasaragic E, Parsons TJ
Journal:Methods Mol Biol
PubMed ID:22139661
STR analysis of DNA extracted from skeletal samples can play an important role in the identification of missing persons. Here we present a method for the extraction of DNA from skeletal samples involving complete demineralization and digestion of the sample, followed by purification by silica binding. This method, together with ... More
Lentiviral transduction and clonal selection of hESCs with endothelial-specific transgenic reporters.
Authors:James D, Zhan Q, Kloss C, Zaninovic N, Rosenwaks Z, Rafii S
Journal:Curr Protoc Stem Cell Biol
PubMed ID:21509935
Generation of vascular endothelial cells (EC) from human embryonic stem cells (hESC) is a vital component of cell-based strategies for treatment of cardiovascular disease. Before hESC-derived ECs can be administered in therapeutic modalities, however, chemically defined culture conditions must be developed that reproducibly and robustly induce vascular differentiation. One approach ... More