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Popis: The GLTP (glycolipid transfer protein) superfamily is defined by a unique lipid transfer/binding fold (GLTP fold) that accelerate glycolipid intermembrane transfer. GLTPD2 is a 291 amino acid protein that belongs to the GLTP family. The gene encoding GLTPD2 maps to human chromosome 17, which comprises over 2.5% of the human genome and encodes over 1,200 genes. Two key tumor suppressor genes are associated with chromosome 17, p53 and BRCA1. Malfunction or loss of p53 expression is associated with malignant cell growth and Li-Fraumeni syndrome. Neurofibromatosis, a condition characterized by neural and epidermal lesions, and dysregulated Schwann cell growth are both linked to mutations on chromosome 17. Alexander disease, Birt-Hogg-Dube syndrome and Canavan disease are also associated with chromosome 17.

Katalogové číslo: BOSSBS-9557R

Měrná jednotka: 1 * 100 µl

Dodavatel: Bioss

Akce

Popis: 1-Boc-piperidin-4-ylboronic acid pinacol ester 97%

Katalogové číslo: ACRO456050050

Měrná jednotka: 1 * 5 g

Dodavatel: Thermo Fisher Scientific

Akce

Popis: Suppresses nitric oxide lysis of pancreatic islet cells.

Katalogové číslo: APOSBIF6401-5G

Měrná jednotka: 1 * 5 g

Dodavatel: Apollo Scientific

Akce

Popis: The protein encoded by this gene is a member of the keratin family. The keratins are intermediate filament proteins responsible for the structural integrity of epithelial cells and are subdivided into cytokeratins and hair keratins. The type I cytokeratins consist of acidic proteins which are arranged in pairs of heterotypic keratin chains. Unlike its related family members, this smallest known acidic cytokeratin is not paired with a basic cytokeratin in epithelial cells. It is specifically expressed in the periderm, the transiently superficial layer that envelopes the developing epidermis. The type I cytokeratins are clustered in a region of chromosome 17q12-q21.<be>This gene encodes the type I intermediate filament chain keratin 17, expressed in nail bed, hair follicle, sebaceous glands, and other epidermal appendages. Mutations in this gene lead to Jackson-Lawler type pachyonychia congenita and steatocystoma multiplex. [provided by RefSeq, Aug 2008].

Katalogové číslo: BOSSBS-11185R

Měrná jednotka: 1 * 100 µl

Dodavatel: Bioss

Akce

Popis: N-(α)-Boc-DL-2,3-diaminopropionic acid 97%

Katalogové číslo: H52811.06

Měrná jednotka: 1 * 5 g

Dodavatel: Thermo Fisher Scientific

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Popis: Octan lithný dihydrát 98% p.a.

Katalogové číslo: ACRO447710010

Měrná jednotka: 1 * 1 kg

Dodavatel: Thermo Fisher Scientific

Bezpečnostní list Akce

Popis: 4-Aminobenzhydrazide 95%

Katalogové číslo: ACRO103200050

Měrná jednotka: 1 * 5 g

Dodavatel: Thermo Fisher Scientific

Bezpečnostní list Akce

Popis: (R)-2-((tert-Butoxycarbonyl)amino)-3,3-dimethylbutanoic acid 95%

Katalogové číslo: H62473.03

Měrná jednotka: 1 * 1 g

Dodavatel: Thermo Fisher Scientific

Certifikáty Akce

Popis: (R)-1-Boc-piperidine-2-carboxylic acid

Katalogové číslo: APOSOR8030-100G

Měrná jednotka: 1 * 100 g

Dodavatel: Apollo Scientific

Akce

Popis: (R)-2-((tert-Butoxycarbonyl)amino)-3,3-dimethylbutanoic acid

Katalogové číslo: APOSBICR124-1G

Měrná jednotka: 1 * 1 g

Dodavatel: Apollo Scientific

Akce

Popis: Fmoc-L-β-homoaspartic acid-gamma-t-butyl ester 95%

Katalogové číslo: H52190.MD

Měrná jednotka: 1 * 250 mg

Dodavatel: Thermo Fisher Scientific

Bezpečnostní list Certifikáty Akce

Popis: The GLTP (glycolipid transfer protein) superfamily is defined by a unique lipid transfer/binding fold (GLTP fold) that accelerate glycolipid intermembrane transfer. GLTPD2 is a 291 amino acid protein that belongs to the GLTP family. The gene encoding GLTPD2 maps to human chromosome 17, which comprises over 2.5% of the human genome and encodes over 1,200 genes. Two key tumor suppressor genes are associated with chromosome 17, p53 and BRCA1. Malfunction or loss of p53 expression is associated with malignant cell growth and Li-Fraumeni syndrome. Neurofibromatosis, a condition characterized by neural and epidermal lesions, and dysregulated Schwann cell growth are both linked to mutations on chromosome 17. Alexander disease, Birt-Hogg-Dube syndrome and Canavan disease are also associated with chromosome 17.

Katalogové číslo: BOSSBS-9557R-CY3

Měrná jednotka: 1 * 100 µl

Dodavatel: Bioss

Akce

Popis: The GLTP (glycolipid transfer protein) superfamily is defined by a unique lipid transfer/binding fold (GLTP fold) that accelerate glycolipid intermembrane transfer. GLTPD2 is a 291 amino acid protein that belongs to the GLTP family. The gene encoding GLTPD2 maps to human chromosome 17, which comprises over 2.5% of the human genome and encodes over 1,200 genes. Two key tumor suppressor genes are associated with chromosome 17, p53 and BRCA1. Malfunction or loss of p53 expression is associated with malignant cell growth and Li-Fraumeni syndrome. Neurofibromatosis, a condition characterized by neural and epidermal lesions, and dysregulated Schwann cell growth are both linked to mutations on chromosome 17. Alexander disease, Birt-Hogg-Dube syndrome and Canavan disease are also associated with chromosome 17.

Katalogové číslo: BOSSBS-9557R-HRP

Měrná jednotka: 1 * 100 µl

Dodavatel: Bioss

Akce

Popis: Bile salt.

Katalogové číslo: APOSBIB6061-10G

Měrná jednotka: 1 * 10 g

Dodavatel: Apollo Scientific

Akce

Popis: C17orf87 (chromosome 17 open reading frame 87) is a 145 amino acid protein that is encoded by a gene mapping to human chromosome 17. Chromosome 17 makes up over 2.5% of the human genome with about 81 million bases encoding over 1,200 genes. Two key tumor suppressor genes are associated with chromosome 17, namely, p53 and BRCA1. Tumor suppressor p53 is necessary for maintenance of cellular genetic integrity by moderating cell fate through DNA repair versus cell death. Malfunction or loss of p53 expression is associated with malignant cell growth and Li-Fraumeni syndrome. Like p53, BRCA1 is directly involved in DNA repair, specifically it is recognized as a genetic determinant of early onset breast cancer and predisposition to cancers of the ovary, colon, prostate gland and fallopian tubes. Chromosome 17 is also linked to neurofibromatosis, a condition characterized by neural and epidermal lesions, and dysregulated Schwann cell growth. Alexander disease, Birt-Hogg-Dube syndrome and Canavan disease are also associated with chromosome 17.

Katalogové číslo: BOSSBS-13685R

Měrná jednotka: 1 * 100 µl

Dodavatel: Bioss

Akce

Popis: trans,trans-Muconic acid (trans,trans-1,3-butadiene-1,4-dicarboxylic acid) ≥98%

Katalogové číslo: L03987.06

Měrná jednotka: 1 * 5 g

Dodavatel: Thermo Fisher Scientific

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