This product is a 1 mg/mL solution of BSA in 0.15 M NaCl. There are no anticipated problems with further diluting in Tris-based or other aqueous buffer solutions for blocking purposes.
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Wybierz wielkość
| Gabaryty przesyłki | SKU | Dostępność | Cena netto |
|---|---|---|---|
| 5 amp | Skontaktuj się z Obsługą Klienta, aby uzyskać informacje na temat dostępności | 237,00 zł | |
| 10 amp | Skontaktuj się z Obsługą Klienta, aby uzyskać informacje na temat dostępności | 413,00 zł |
Informacje o tej pozycji
237,00 zł
biological source
bovine
Quality Segment
form
liquid
contains
0.05% sodium azide as preservative
packaging
ampule of 1 mL
concentration
0.98—1.02 mg protein/mL
technique(s)
ELISA: suitable
color
clear colorless
UniProt accession no.
storage temp.
2-8°C
Gene Information
bovine ... ALB(280717)
Application
Protein standard for all protein assays. The sealed ampules provide assurance that the concentration will be correct with every assay.
Packaging
Other Notes
1 of 1
Ta pozycja | |||
|---|---|---|---|
| biological source bovine | biological source - | biological source bovine serum | biological source - |
| technique(s) ELISA: suitable | technique(s) microbiological culture: suitable | technique(s) cell culture | mammalian: suitable, microbiological culture: suitable | technique(s) ELISA: suitable, enzyme immunoassay: suitable |
| Quality Level 200 | Quality Level 300 | Quality Level 300 | Quality Level 300 |
| form liquid | form lyophilized powder | form lyophilized powder | form solution (30%) |
| Gene Information bovine ... ALB(280717) | Gene Information - | Gene Information - | Gene Information - |
| storage temp. 2-8°C | storage temp. - | storage temp. - | storage temp. 2-8°C |
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Klasa składowania
12 - Non Combustible Liquids
flash_point_f
Not applicable
flash_point_c
Not applicable
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Protokoły
Standardowa procedura ilościowego oznaczania stężenia białka całkowitego w roztworze metodą BCA.
To standardize a procedure for the determination of protein by modified Lowry.
To determine protein content, the Warburg-Christian method refers to measuring protein samples at 280 nm using a spectrophotometer.
Produkty
Zestaw do szybkiego trawienia trypsyną zapewnia wiarygodne wyniki analizy spektrometrii masowej w czasie krótszym niż 2 godziny.
Rapid trypsin digest kit yields reliable results in less than 2 hours for mass spectrometry analysis.
Powiązane treści
Protein quantification methods, reagents, and immunoassay technology for accurately measuring the protein concentrations in a variety of samples.
Metody kwantyfikacji białek, odczynniki i technologia testów immunologicznych do dokładnego pomiaru stężenia białek w różnych próbkach.
Numer pozycji handlu globalnego
| SKU | NUMER GTIN |
|---|---|
| P0914-5AMP | 04061835558230 |
| P0914-5AMP-KC | 04061833694381 |
| P0914-10AMP | 04061835558223 |
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Can bsa P0914-5AMP be diluted in tbs-t to make block buffer for electrophoresis?
1 answer-
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What is the shipping temperature?
1 answer-
The item is shipped at ambient temperature. A transit time of up to 2 weeks will not impact the quality of this material. Upon delivery, this product should be stored at 2-8°C.
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What is the Department of Transportation shipping information for this product?
1 answer-
Transportation information can be found in Section 14 of the product's (M)SDS.To access the shipping information for this material, use the link on the product detail page for the product.
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Do you have any information on the traceability to a recognized protein standard, such as NIST? Or is the concentration derived from accepted values of natural physical constants?
1 answer-
The concentration of each lot of the protein standard, Product P0914, is determined by UV measurements. Specifically, given a known extinction coefficient (E) and a measured absorbance (A), and assuming a standard pathlength of 1 cm, the concentration (c) can be determined by Beer's Law (c = A/E). The assay result is derived from an accepted value of a natural physical constant. Specifically, the E1% of 6.67 at approximately 279 nm is a well-accepted value, originally published in J. Am. Chem. Soc., 78, 3656-3660 (1956).
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