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


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Product Image-115-9266

Notitieboeken voor het laboratorium, Nalgene®

Leverancier: Thermo Fisher Scientific
Omschrijving: Omslag van polyethyleen voor duurzaamheid in laboratoriumomgevingen.

Environmentally Preferable

Image Unavailable-8.20061.0050

2-Aminoethyl dihydrogen phosphate for synthesis, Sigma-Aldrich®

Leverancier: Merck
Omschrijving: 2-Aminoethyl dihydrogen phosphate for synthesis, Sigma-Aldrich®

MSDS Certificaten

Product Image-1.04875.1000

Potassium dihydrogen phosphate 1/15 mol/l in aqueous solution, Supelco®

Catalogus nummer: (1.04875.1000)
Leverancier: Merck
Omschrijving: Potassium dihydrogen phosphate 1/15 mol/l in aqueous solution, Supelco®
UOM: 1 * 1 L

MSDS


Product Image-BSBTPB9684

Anti-APBB1 Rabbit Polyclonal Antibody

Catalogus nummer: (BSBTPB9684)
Leverancier: Boster Bio
Omschrijving: Rabbit IgG polyclonal antibody for Amyloid beta A4 precursor protein-binding family B member 1(APBB1) detection. Tested with WB, IHC-P in Human;Mouse;Rat.
UOM: 1 * 1 EA
Image Unavailable-1.04873.9025

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

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

MSDS Certificaten Sale

Image Unavailable-1048255.

Balsalazide Disodium, Reference Standard

Catalogus nummer: (1048255.)
Leverancier: USP
Omschrijving: USP Reference Standards are specified for use in conducting official USP–NF tests and assays. USP also provides Reference Standards specified in the Food Chemicals Codex as well as authentic substances—high-quality chemical samples—as a service to analytical, clinical, pharmaceutical and research laboratories. To confirm accuracy and reproducibility, USP Reference Standards are rigorously tested and evaluated by multiple independent laboratories including USP, commercial, regulatory, and academic labs. USP also provide publicly available, official documentary standards for pharmaceutical ingredients in the USP–NF that link directly with our primary reference standards.
UOM: 1 * 200 mg
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

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
Image Unavailable-1233009.

Edetate Disodium, Reference Standard

Catalogus nummer: (1233009.)
Leverancier: USP
Omschrijving: USP Reference Standards are specified for use in conducting official USP–NF tests and assays. USP also provides Reference Standards specified in the Food Chemicals Codex as well as authentic substances—high-quality chemical samples—as a service to analytical, clinical, pharmaceutical and research laboratories. To confirm accuracy and reproducibility, USP Reference Standards are rigorously tested and evaluated by multiple independent laboratories including USP, commercial, regulatory, and academic labs. USP also provide publicly available, official documentary standards for pharmaceutical ingredients in the USP–NF that link directly with our primary reference standards.
UOM: 1 * 200 mg
Image Unavailable-5.43841.0250

Potassium dihydrogen phosphate, watervrij ≥99.5% (by acidimetry), LiChropur™ for HPLC, Supelco®

Leverancier: Merck
Omschrijving: Potassium dihydrogen phosphate, anhydrous ≥99.5% (by acidimetry), LiChropur™ for HPLC, Supelco®

Certificaten

Image Unavailable-BOSSBS-9380R-CY3

Anti-MID1 Rabbit Polyclonal Antibody (Cy3®)

Catalogus nummer: (BOSSBS-9380R-CY3)
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-A488

Anti-MID1 Rabbit Polyclonal Antibody (Alexa Fluor® 488)

Catalogus nummer: (BOSSBS-9380R-A488)
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-11293R-A555

Anti-HOXA4 Rabbit Polyclonal Antibody (Alexa Fluor® 555)

Catalogus nummer: (BOSSBS-11293R-A555)
Leverancier: Bioss
Omschrijving: The Hox homeobox genes encode proteins that are transcriptional regulators with an established role in embryonic development. HoxA4 (homeobox A4), also known as HOX1D or HOX1, is a 320 amino acid protein that localizes to the nucleus and contains one homeobox DNA-binding domain. Expressed in the embryonic nervous system, HoxA4 functions as a sequence-specific DNA-binding transcription factor that is part of a regulatory mechanism that provides cells with positional identities during development. Via its ability to bind DNA, HoxA4 plays an important role in the regulation of gene expression, as well as morphogenesis and differentiation. The gene encoding HoxA4 maps to human chromosome 7, which houses over 1,000 genes and comprises nearly 5% of the human genome. Defects in some of the genes localized to chromosome 7 have been linked to Osteogenesis imperfecta, Williams-Beuren syndrome, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome.
UOM: 1 * 100 µl
Image Unavailable-1802-50ML

Naphthol AS-BI phosphate solution 4 g/L in methanol stabilised, Sigma-Aldrich®

Catalogus nummer: (1802-50ML)
Leverancier: SIGMA ALDRICH MICROSCOPY
Omschrijving: Naphthol AS-BI Phosphoric acid solution for use in the Sigma Lymphocyte Enzyme (Acid Phosphatase) Procedure, No. 181A.
UOM: 1 * 50 mL
Image Unavailable-BOSSBS-9380R-CY5.5

Anti-MID1 Rabbit Polyclonal Antibody (Cy5.5®)

Catalogus nummer: (BOSSBS-9380R-CY5.5)
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
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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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