Wyszukano: WERNER+MERTZ

Numer katalogowy: (ABCAAB200-100)

Producent: Abcam

Opis: Anti-Werner's syndrome helicase WRN Rabbit Polyclonal Antibody

j.m.: 1 * 100 µl

MSDS Wyprzedaż

Numer katalogowy: (ABCAAB17987-100)

Producent: Abcam

Opis: Rabbit polyclonal to Werner's syndrome helicase WRN.

j.m.: 1 * 100 µG

Wyprzedaż

Numer katalogowy: (ANTIA10013-100)

Producent: ANTIBODIES.COM

Opis: Rabbit polyclonal antibody to Werner's syndrome helicase WRN for WB with samples derived from human.

j.m.: 1 * 100 µl

New Product Wyprzedaż

Producent: Abcam

Opis: Rabbit monoclonal [EPR6392] to Werner's syndrome helicase WRN.

New Product

Numer katalogowy: (ABCAAB230851-200)

Producent: Abcam

Opis: Rabbit polyclonal to Werner's syndrome helicase WRN.

j.m.: 1 * 200 µl

Wyprzedaż

Numer katalogowy: (SCTV106660)

Producent: S.C.A.T.

Opis: This purging manifold alows you to install up to four SafetyCaps on your purging bottle.

j.m.: 1 * 1 SZT

Wyprzedaż

Numer katalogowy: (TANA713469)

Producent: WERNER MERTZ

Opis: A range of cleaners suitable for most maintenance cleaning tasks in rest rooms.

j.m.: 1 * 750 mL

Wyprzedaż

Numer katalogowy: (USBIW9000-03)

Producent: US Biological

Opis: Anti-WRN Mouse Monoclonal Antibody [clone: 11C960]

j.m.: 1 * 100 µG

Wyprzedaż

Numer katalogowy: (ABCAAB112372-2)

Producent: Abcam

Opis: WERNER'S SYNDROME HELICASE WRN PROTEIN 1 * 2 µG

j.m.: 1 * 2 µG

Wyprzedaż

Numer katalogowy: (ABCAAB287126-5)

Producent: Abcam

Opis: [EN][EN]A WERNER SYNDROME HELICASE (WRN) 1 * 5 mg

j.m.: 1 * 5 mg

Wyprzedaż

Numer katalogowy: (BSBTPB10107)

Producent: Boster Bio

Opis: Rabbit IgG polyclonal antibody for Werner syndrome ATP-dependent helicase(WRN) detection. Tested with WB in Human;Rat.

j.m.: 1 * 100 µG

Wyprzedaż

Numer katalogowy: (PRSI28-498)

Producent: ProSci Inc.

Opis: Werner's syndrome is a rare autosomal recessive disorder characterized by premature aging. The protein encoded by this gene interacts with the N-terminal portion of Werner protein containing the exonuclease domain. This protein shows homology to replication factor C family proteins, and is conserved from E. coli to human. Studies in yeast suggest that this gene may influence the aging process. Two transcript variants encoding different isoforms have been isolated for this gene.Werner's syndrome is a rare autosomal recessive disorder characterized by premature aging. The protein encoded by this gene interacts with the N-terminal portion of Werner protein containing the exonuclease domain. This protein shows homology to replication factor C family proteins, and is conserved from E. coli to human. Studies in yeast suggest that this gene may influence the aging process. Two transcript variants encoding different isoforms have been isolated for this gene.

j.m.: 1 * 50 µG

Wyprzedaż

Numer katalogowy: (PRSI55-290)

Producent: ProSci Inc.

Opis: The exact function of this gene is not known, however, its encoded product is highly similar to purine-rich element binding protein A. The latter is a DNA-binding protein which binds preferentially to the single strand of the purine-rich element termed PUR, and has been implicated in the control of both DNA replication and transcription. PURG lies in close proximity to the Werner syndrome gene, but on the opposite strand, on chromosome 8p11. Two transcript variants encoding different isoforms have been found for this gene.

j.m.: 1 * 400 µl

Wyprzedaż

Numer katalogowy: (BOSSBS-8292R-CY7)

Producent: Bioss

Opis: Made up of nearly 146 million bases, chromosome 8 encodes about 800 genes. Translocation of portions of chromosome 8 with amplifications of the c-Myc gene are found in some leukemias and lymphomas, and typically associated with a poor prognosis. Portions of chromosome 8 have been linked to schizophrenia and bipolar disorder. Trisomy 8, also known as Warkany syndrome 2, most often results in early miscarriage but is occasionally seen in a mosaic form in surviving patients who suffer to a varying degree from a number of symptoms including retarded mental and motor development, and certain facial and developmental defects. WRN is a DNA helicase encoded by chromosome 8 and shown defective in those with the early aging disorder Werner syndrome. Chromosome 8 is also associated with Pfeiffer syndrome, congenital hypothyroidism and Waardenburg syndrome.

j.m.: 1 * 100 µl

Wyprzedaż

Numer katalogowy: (BOSSBS-9395R)

Producent: Bioss

Opis: Made up of nearly 146 million bases, chromosome 8 encodes about 800 genes. Translocation of portions of chromosome 8 with amplifications of the c-Myc gene are found in some leukemias and lymphomas, and typically associated with a poor prognosis. Portions of chromosome 8 have been linked to schizophrenia and bipolar disorder. Trisomy 8, also known as Warkany syndrome 2, most often results in early miscarriage but is occasionally seen in a mosaic form in surviving patients who suffer to a varying degree from a number of symptoms including retarded mental and motor development, and certain facial and developmental defects. WRN is a DNA helicase encoded by chromosome 8 and shown defective in those with the early aging disorder Werner syndrome. Chromosome 8 is also associated with Pfeiffer syndrome, congenital hypothyroidism and Waardenburg syndrome.

j.m.: 1 * 100 µl

Wyprzedaż

Numer katalogowy: (BOSSBS-8292R-A488)

Producent: Bioss

Opis: Made up of nearly 146 million bases, chromosome 8 encodes about 800 genes. Translocation of portions of chromosome 8 with amplifications of the c-Myc gene are found in some leukemias and lymphomas, and typically associated with a poor prognosis. Portions of chromosome 8 have been linked to schizophrenia and bipolar disorder. Trisomy 8, also known as Warkany syndrome 2, most often results in early miscarriage but is occasionally seen in a mosaic form in surviving patients who suffer to a varying degree from a number of symptoms including retarded mental and motor development, and certain facial and developmental defects. WRN is a DNA helicase encoded by chromosome 8 and shown defective in those with the early aging disorder Werner syndrome. Chromosome 8 is also associated with Pfeiffer syndrome, congenital hypothyroidism and Waardenburg syndrome.

j.m.: 1 * 100 µl

Wyprzedaż