Du sökte efter: WERNER+MERTZ

Artikel nummer : (ABCAAB200-100)

Leverantör: Abcam

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

UOM: 1 * 100 µl

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Artikel nummer : (ABCAAB17987-100)

Leverantör: Abcam

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

UOM: 1 * 100 µG

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Artikel nummer : (ABCAAB124673-100)

Leverantör: Abcam

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

UOM: 1 * 100 µl

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Artikel nummer : (ANTIA10013-100)

Leverantör: ANTIBODIES.COM

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

UOM: 1 * 100 µl

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Artikel nummer : (ABCAAB230851-200)

Leverantör: Abcam

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

UOM: 1 * 200 µl

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Artikel nummer : (ABCAAB241545-100)

Leverantör: Abcam

Beskrivning: Mouse monoclonal [195C] to Werner's syndrome helicase WRN.

UOM: 1 * 100 µG

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Leverantör: Abcam

Beskrivning: Rabbit monoclonal [EPR6392] to Werner's syndrome helicase WRN - BSA and Azide free.

Artikel nummer : (ABCAAB252781-100UG)

Leverantör: Abcam

Beskrivning: Mouse monoclonal [195C] to Werner's syndrome helicase WRN - BSA and Azide free.

UOM: 1 * 100 µG

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Artikel nummer : (SCTV106660)

Leverantör: S.C.A.T.

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

UOM: 1 * 1 Items

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Artikel nummer : (USBIW9000-03)

Leverantör: US Biological

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

UOM: 1 * 100 µG

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Artikel nummer : (ABCAAB112372-2)

Leverantör: Abcam

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

UOM: 1 * 2 µG

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Artikel nummer : (ABCAAB287126-5)

Leverantör: Abcam

Beskrivning: A WERNER SYNDROME HELICASE (WRN) INHIBIT 1 * 5 mg

UOM: 1 * 5 mg

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Artikel nummer : (BSBTPB10107)

Leverantör: Boster Bio

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

UOM: 1 * 100 µG

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Artikel nummer : (PRSI28-498)

Leverantör: ProSci Inc.

Beskrivning: 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.

UOM: 1 * 50 µG

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Artikel nummer : (PRSI55-290)

Leverantör: ProSci Inc.

Beskrivning: 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.

UOM: 1 * 400 µl

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Artikel nummer : (BOSSBS-8292R-CY7)

Leverantör: Bioss

Beskrivning: 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.

UOM: 1 * 100 µl

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