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Image non disponible-BOSSBS-8578R-A350

Anti-GRAMD2 Rabbit Polyclonal Antibody (Alexa Fluor® 350)

Numéro de catalogue: (BOSSBS-8578R-A350)
Fournisseur: Bioss
Description: GRAMD2 is a 354 amino acid single-pass membrane protein that contains one GRAM domain and is encoded by a gene that maps to human chromosome 15q23. Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and is about 3% of the human genome. Angelman and Prader-Willi syndromes are associated with loss of function or deletion of genes in the 15q11-q13 region. In the case of Angelman syndrome, this loss is due to inactivity of the maternal 15q11-q13 encoded UBE3A gene in the brain by either chromosomal deletion or mutation. In cases of Prader-Willi syndrome, there is a partial or complete deletion of this region from the paternal copy of chromosome 15. Tay-Sachs disease is a lethal disorder associated with mutations of the HEXA gene, which is encoded by chromosome 15. Marfan syndrome is associated with chromosome 15 through the FBN1 gene.
UOM: 1 * 100 µl
Image non disponible-BOSSBS-8578R-A488

Anti-GRAMD2 Rabbit Polyclonal Antibody (Alexa Fluor® 488)

Numéro de catalogue: (BOSSBS-8578R-A488)
Fournisseur: Bioss
Description: GRAMD2 is a 354 amino acid single-pass membrane protein that contains one GRAM domain and is encoded by a gene that maps to human chromosome 15q23. Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and is about 3% of the human genome. Angelman and Prader-Willi syndromes are associated with loss of function or deletion of genes in the 15q11-q13 region. In the case of Angelman syndrome, this loss is due to inactivity of the maternal 15q11-q13 encoded UBE3A gene in the brain by either chromosomal deletion or mutation. In cases of Prader-Willi syndrome, there is a partial or complete deletion of this region from the paternal copy of chromosome 15. Tay-Sachs disease is a lethal disorder associated with mutations of the HEXA gene, which is encoded by chromosome 15. Marfan syndrome is associated with chromosome 15 through the FBN1 gene.
UOM: 1 * 100 µl
Image non disponible-J62834.03

Gentamicine, sulfate (sel) 600 IU/mg

Fournisseur: Thermo Fisher Scientific
Description: Gentamycin Sulfate is a broad-spectrum, aminoglycoside antibiotic used for cell culture which inhibits protein synthesis in sensitive organisms. Reported to have activity against gram-negative bacteria, Pseudomonas aeruginosa, gram-positive Staphylococcus aureus and some mycoplasmas. Reported to have low toxicity to mammalian cells and viruses at certain concentrations, useful for long-term tissue culture studies with viruses.

MSMD Certificats

Image non disponible-J61763.06

Polymyxine B, sulfate, Qualité Culture Cellulaire

Fournisseur: Thermo Fisher Scientific
Description: Antibiotic for Gram-negative bacteria

MSMD Certificats

Image non disponible-BOSSBS-8578R-A680

Anti-GRAMD2 Rabbit Polyclonal Antibody (Alexa Fluor® 680)

Numéro de catalogue: (BOSSBS-8578R-A680)
Fournisseur: Bioss
Description: GRAMD2 is a 354 amino acid single-pass membrane protein that contains one GRAM domain and is encoded by a gene that maps to human chromosome 15q23. Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and is about 3% of the human genome. Angelman and Prader-Willi syndromes are associated with loss of function or deletion of genes in the 15q11-q13 region. In the case of Angelman syndrome, this loss is due to inactivity of the maternal 15q11-q13 encoded UBE3A gene in the brain by either chromosomal deletion or mutation. In cases of Prader-Willi syndrome, there is a partial or complete deletion of this region from the paternal copy of chromosome 15. Tay-Sachs disease is a lethal disorder associated with mutations of the HEXA gene, which is encoded by chromosome 15. Marfan syndrome is associated with chromosome 15 through the FBN1 gene.
UOM: 1 * 100 µl
Image du produit-HACH253334

Nitrification inhibitor for BOD

Numéro de catalogue: (HACH253334)
Fournisseur: Hach
Description: TCMP - 2-chloro-6 (trichloromethyl) pyridine (N-Serve), coated on an inert substrate.
UOM: 1 * 500 g

Certificats


Image non disponible-ICNA0215594925

Norfloxacin, poudre jaune pâle

Fournisseur: MP Biomedicals
Description: A synthetic fluoroquinolone antibiotic used to treat urinary tract infections. It is effective against gram-positive and gram-negative bacteria, and its’ mode of action is to inhibit DNA gyrase and topoisomerase IV, thus
preventing cell division.

Image non disponible-BOSSBS-8578R-CY7

Anti-GRAMD2 Rabbit Polyclonal Antibody (Cy7®)

Numéro de catalogue: (BOSSBS-8578R-CY7)
Fournisseur: Bioss
Description: GRAMD2 is a 354 amino acid single-pass membrane protein that contains one GRAM domain and is encoded by a gene that maps to human chromosome 15q23. Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and is about 3% of the human genome. Angelman and Prader-Willi syndromes are associated with loss of function or deletion of genes in the 15q11-q13 region. In the case of Angelman syndrome, this loss is due to inactivity of the maternal 15q11-q13 encoded UBE3A gene in the brain by either chromosomal deletion or mutation. In cases of Prader-Willi syndrome, there is a partial or complete deletion of this region from the paternal copy of chromosome 15. Tay-Sachs disease is a lethal disorder associated with mutations of the HEXA gene, which is encoded by chromosome 15. Marfan syndrome is associated with chromosome 15 through the FBN1 gene.
UOM: 1 * 100 µl
Image non disponible-BOSSBS-8578R-FITC

Anti-GRAMD2 Rabbit Polyclonal Antibody (FITC (Fluorescein Isothiocyanate))

Numéro de catalogue: (BOSSBS-8578R-FITC)
Fournisseur: Bioss
Description: GRAMD2 is a 354 amino acid single-pass membrane protein that contains one GRAM domain and is encoded by a gene that maps to human chromosome 15q23. Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and is about 3% of the human genome. Angelman and Prader-Willi syndromes are associated with loss of function or deletion of genes in the 15q11-q13 region. In the case of Angelman syndrome, this loss is due to inactivity of the maternal 15q11-q13 encoded UBE3A gene in the brain by either chromosomal deletion or mutation. In cases of Prader-Willi syndrome, there is a partial or complete deletion of this region from the paternal copy of chromosome 15. Tay-Sachs disease is a lethal disorder associated with mutations of the HEXA gene, which is encoded by chromosome 15. Marfan syndrome is associated with chromosome 15 through the FBN1 gene.
UOM: 1 * 100 µl
Image non disponible-ICNA0215494780

Cefotaxime sodium salt ≥95%, poudre blanc cassé

Fournisseur: MP Biomedicals
Description: Cefotaxime is a cephalosporin, which acts by interference of synthesis of peptidoglycan of the bacterial cell wall. Cefotaxime, a cephalosporin antibiotic, is active against both gram-negative and gram-positive bacteria. In addition, cefotaxime blocks the division of cyanobacteria and lower plant organelles/plastids such as the photosynthetic organelles of Glaucophytes and chloroplasts of bryophytes.
Cefotaxime is used for infections of the respiratory tract, skin, bones, joints, urogenital system, meninges, and bloodstream. It generally has good coverage against most Gram-negative bacteria, with the notable exception of Pseudomonas. It is also effective against most Gram-positive cocci except for Enterococcus. It is active against penicillin-resistant strains of Streptococcus pneumoniae. It has modest activity against the anaerobic Bacteroides fragilis. In meningitis, cefotaxime crosses the blood–brain barrier better than cefuroxime.
Cefotaxim inhibits bacterial cell wall synthesis by binding to penicillin-binding proteins (PBPs) which inhibits the final transpeptidation step of peptidoglycan synthesis in bacterial cell walls. As a result, bacteria lyse due to cell wall autolytic enzymes.

Certificats

Image non disponible-ICNA0215583905

Nisin (de Lactococcus lacti)

Fournisseur: MP Biomedicals
Description: Nisin is a polycyclic lantibiotic produced by <i>Lactococcus lactis</i>. It is an antibiotic with bactericidal action and is commonly used as a food preservative. It is also used as a selective agent in cell culture for the isolation of gram-negative bacteria, yeast, and moulds.

Image non disponible-J66460.06

Ceftazidime pentahydrate 95%

Fournisseur: Thermo Fisher Scientific
Description: Targets primarily Gram-negative bacteria especially Pseudomonas aeruginosa unlike other third generation cephalosporins.

MSMD Certificats

Image du produit-LIED782D

Biology prepared microscope slides, school set D

Numéro de catalogue: (LIED782D)
Fournisseur: LIEDER JOHANNES
Description: The slides are arranged and compiled, so that each enlarges the subject line of the proceeding one.
UOM: 1 * 1 ST
Image non disponible-ICNA0215671180

Sulphamethoxazole, poudre blanche

Fournisseur: MP Biomedicals
Description: Sulphonamide antibiotic that blocks the synthesis of dihydrofolic acid by inhibiting the enzyme dihydropteroate synthase. Mode of Action: Inhibits folic acid synthesis in prokaryotes. Anti-microbial Spectrum: Gram positive, Gram negative, Chlamydia. Mode of Resistance: Alteration of dihydropteroate synthase or alternative pathway for folic acid synthesis.

Image du produit-STMC100-0818

Wheat Germ Agglutinin (WGA), iFluor™ 647

Numéro de catalogue: (STMC100-0818)
Fournisseur: STEMCELL Technologies
Description: Fluorescent dye conjugates for staining cell membranes of gram-positive bacteria, mammalian cells, and yeast bud scars - 1000 µg.
UOM: 1 * 1 EA

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Image non disponible-AATB24305

GTIF647 [iFluor® 647 gentamicin conjugate]

Fournisseur: AAT BIOQUEST
Description: Gentamicin is widely used for treating tuberculosis and Gram-negative infections and is particularly useful in neonatal intensive care units.

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