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U heeft gezocht op: Combretastatin+A4+Phosphate+disodium+salt


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Triphenyl phosphate for synthesis, Sigma-Aldrich®

Leverancier: Merck
Omschrijving: Triphenyl phosphate for synthesis, Sigma-Aldrich®

MSDS

Image Unavailable-8.14181.0250

Bis(2-ethylhexyl)phosphate for synthesis

Leverancier: Merck
Omschrijving: Bis(2-ethylhexyl)phosphate for synthesis

MSDS

Image Unavailable-86899-6X1AMP-F

Tetrabutylammonium dihydrogen phosphate for ion pair chromatography, Supelco®

Catalogus nummer: (86899-6X1AMP-F)
Leverancier: Merck
Omschrijving: Tetrabutylammonium dihydrogen phosphate for ion pair chromatography, Supelco®
UOM: 1 * 1 Kit
Image Unavailable-855-20ML

Naphthol AS-MX phosphate, Sigma-Aldrich®

Catalogus nummer: (855-20ML)
Leverancier: SIGMA ALDRICH MICROSCOPY
Omschrijving: Naphthol AS-MX phosphate, Sigma-Aldrich®
UOM: 1 * 20 mL
Image Unavailable-8.21202.1000

Tris(2-ethylhexyl)phosphate for synthesis, Sigma-Aldrich®

Leverancier: Merck
Omschrijving: Tris(2-ethylhexyl)phosphate for synthesis, Sigma-Aldrich®

MSDS

Product Image-GAINA4RCL-23T1-GA

Removable Cryogenic Labels for Laser Printers

Leverancier: GA
Omschrijving: Removable cryo labels provided in A4 sheet format for printing with laser printers. Ideal for long-term storage in liquid phase and vapor phase liquid nitrogen (−196 °C), lab freezers (−80 °C), and on dry ice.

Product Image-ANTIA99112-100

Anti-Eph receptor A2+A3+A4 Rabbit Polyclonal Antibody

Catalogus nummer: (ANTIA99112-100)
Leverancier: ANTIBODIES.COM
Omschrijving: Rabbit polyclonal antibody to EphA2 for WB and ELISA with samples derived from human and mouse.
UOM: 1 * 1 EA

New Product


Image Unavailable-11886.04

Sodium tetrachloropalladate(II) hydraat (30% Pd) ≥99.95% (metals basis)

Leverancier: Thermo Fisher Scientific
Omschrijving: Sodium tetrachloropalladate(II) hydraat (30% Pd) ≥99.95% (metals basis)

MSDS Certificaten

Product Image-SIMEVF2325

Test charts

Leverancier: Industrial Physics
Omschrijving: Test charts are used for testing physical properties of coating, lacquers, and inks.

Product Image-PURUPCIB-1083C

Cleanroom paper, CLEAN image™, Purus

Leverancier: PURUS
Omschrijving: CLEAN image™ cleanroom papers are suitable for writing, printing and photocopying in cleanroom environments. The PE, non-latex binding technology reduces paper fibre.

Image Unavailable-1.04873.9050

Potassium dihydrogen phosphate, EMSURE® ISO for analysis, Supelco®

Leverancier: Merck
Omschrijving: Potassium dihydrogen phosphate, EMSURE® ISO for analysis, Supelco®

MSDS Certificaten Sale

Product Image-GAINA4CL-48T1-RE

Permanent Cryogenic Labels for Laser Printers

Leverancier: GA
Omschrijving: Permanent cryogenic laser labels for long-term storage in liquid phase and vapor phase liquid nitrogen (−196 °C), lab freezers (−80 °C), and on dry ice. Supplied in A4 sheet format for printing in standard desktop laser printers, these cryogenic labels do not jam printers and withstand UV and gamma irradiation.

Image Unavailable-BOSSBS-9380R-A647

Anti-MID1 Rabbit Polyclonal Antibody (Alexa Fluor® 647)

Catalogus nummer: (BOSSBS-9380R-A647)
Leverancier: Bioss
Omschrijving: Midline-1 (Tripartite motif-containing protein 18, Putative transcription factor XPRF, RING finger protein 59) is a 667 amino acid protein encoded by the human gene MID1. Midline-1 belongs to the TRIM/RBCC family and contains two B box-type zinc fingers, one B30.2/SPRY domain, one COS domain, one fibronectin type-III domain and one RING-type zinc finger. Midline-1 is believed to have E3 ubiquitin ligase activity which targets the catalytic subunit of protein phosphatase 2 for degradation. It is a cytoplasmic protein found as a homodimer or heterodimer with Midline-2. It also interacts with IGBP1 (Lymphocyte signaling protein A4). Defects in MID1 are the cause of Opitz syndrome type I (OS-I). OS-I is an X-linked recessive disorder characterized by hypertelorism, genital-urinary defects such as hypospadias in males and splayed labia in females, lip-palate-laryngotracheal clefts, imperforate anus, developmental delay and congenital heart defects. OS-I mutations produce proteins with a decreased affinity for microtubules.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-9380R-CY7

Anti-MID1 Rabbit Polyclonal Antibody (Cy7®)

Catalogus nummer: (BOSSBS-9380R-CY7)
Leverancier: Bioss
Omschrijving: Midline-1 (Tripartite motif-containing protein 18, Putative transcription factor XPRF, RING finger protein 59) is a 667 amino acid protein encoded by the human gene MID1. Midline-1 belongs to the TRIM/RBCC family and contains two B box-type zinc fingers, one B30.2/SPRY domain, one COS domain, one fibronectin type-III domain and one RING-type zinc finger. Midline-1 is believed to have E3 ubiquitin ligase activity which targets the catalytic subunit of protein phosphatase 2 for degradation. It is a cytoplasmic protein found as a homodimer or heterodimer with Midline-2. It also interacts with IGBP1 (Lymphocyte signaling protein A4). Defects in MID1 are the cause of Opitz syndrome type I (OS-I). OS-I is an X-linked recessive disorder characterized by hypertelorism, genital-urinary defects such as hypospadias in males and splayed labia in females, lip-palate-laryngotracheal clefts, imperforate anus, developmental delay and congenital heart defects. OS-I mutations produce proteins with a decreased affinity for microtubules.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-9380R-FITC

Anti-MID1 Rabbit Polyclonal Antibody (FITC (Fluorescein Isothiocyanate))

Catalogus nummer: (BOSSBS-9380R-FITC)
Leverancier: Bioss
Omschrijving: Midline-1 (Tripartite motif-containing protein 18, Putative transcription factor XPRF, RING finger protein 59) is a 667 amino acid protein encoded by the human gene MID1. Midline-1 belongs to the TRIM/RBCC family and contains two B box-type zinc fingers, one B30.2/SPRY domain, one COS domain, one fibronectin type-III domain and one RING-type zinc finger. Midline-1 is believed to have E3 ubiquitin ligase activity which targets the catalytic subunit of protein phosphatase 2 for degradation. It is a cytoplasmic protein found as a homodimer or heterodimer with Midline-2. It also interacts with IGBP1 (Lymphocyte signaling protein A4). Defects in MID1 are the cause of Opitz syndrome type I (OS-I). OS-I is an X-linked recessive disorder characterized by hypertelorism, genital-urinary defects such as hypospadias in males and splayed labia in females, lip-palate-laryngotracheal clefts, imperforate anus, developmental delay and congenital heart defects. OS-I mutations produce proteins with a decreased affinity for microtubules.
UOM: 1 * 100 µl
Product Image-1.05104.9050

di-Potassium hydrogen phosphate, EMSURE® for analysis, Supelco®

Leverancier: Merck
Omschrijving: di-Potassium hydrogen phosphate, EMSURE® for analysis, Supelco®

MSDS Sale

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Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the call is still displayed and you need assistance, please call us at 1-800-932-5000.
This product is marked as restricted and can only be purchased by approved Shipping Accounts. If you need further assistance, email VWR Regulatory Department at Regulatory_Affairs@vwr.com
-Additional Documentation May be needed to purchase this item. A VWR representative will contact you if needed.
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