U heeft gezocht op: Amberlyst®+A-21

13 252 results were found

Verfijn resultaten Sorteren bij

Sort Results

List view Easy View (new)

Vergelijk(0) Clear

Rate These Search Results

Anti-SHANK1 Mouse Monoclonal Antibody [clone: S22-21]

Catalogus nummer: (ABCAAB94576-100)

Leverancier: Abcam

Omschrijving: Anti-SHANK1 Mouse Monoclonal Antibody [clone: S22-21]

UOM: 1 * 1 EA

Sale

N/A Each

Anti-C21orf87 Rabbit Polyclonal Antibody (Alexa Fluor® 750)

Catalogus nummer: (BOSSBS-9982R-A750)

Leverancier: Bioss

Omschrijving: The smallest of the human chromosomes, 21 makes up about 1.5% of the human genome. Chromosome 21 contains nearly 300 genes and 47 million base pairs. Down syndrome, also known as trisomy 21, is the disease most commonly associated with chromosome 21. Alzheimer's disease, Jervell and Lange-Nielsen syndrome and amyotrophic lateral sclerosis are also associated with chromosome 21. Translocations are found to occur between chromosome 21 and 8, and chromosome 21 and 12, in certain leukaemias. The C21orf87 gene product has been provisionally designated C21orf87 pending further characterisation.

UOM: 1 * 100 µl

Sale

N/A Each

Anti-C21orf88 Rabbit Polyclonal Antibody (Cy3®)

Catalogus nummer: (BOSSBS-15130R-CY3)

Leverancier: Bioss

Omschrijving: The smallest of the human chromosomes, 21 makes up about 1.5% of the human genome. Chromosome 21 contains nearly 300 genes and 47 million base pairs. Down syndrome, also known as trisomy 21, is the disease most commonly associated with chromosome 21. Alzheimer's disease, Jervell and Lange-Nielsen syndrome and amyotrophic lateral sclerosis are also associated with chromosome 21. Translocations are found to occur between chromosome 21 and 8, and chromosome 21 and 12, in certain leukemias. The C21orf88 gene product has been provisionally designated C21orf88 pending further characterization.

UOM: 1 * 100 µl

Sale

N/A Each

Anti-C21orf88 Rabbit Polyclonal Antibody

Catalogus nummer: (BOSSBS-15130R)

Leverancier: Bioss

Omschrijving: The smallest of the human chromosomes, 21 makes up about 1.5% of the human genome. Chromosome 21 contains nearly 300 genes and 47 million base pairs. Down syndrome, also known as trisomy 21, is the disease most commonly associated with chromosome 21. Alzheimer's disease, Jervell and Lange-Nielsen syndrome and amyotrophic lateral sclerosis are also associated with chromosome 21. Translocations are found to occur between chromosome 21 and 8, and chromosome 21 and 12, in certain leukemias. The C21orf88 gene product has been provisionally designated C21orf88 pending further characterization.

UOM: 1 * 100 µl

Sale