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Image Unavailable-BOSSBS-15187R-A750

Anti-C4orf17 Rabbit Polyclonal Antibody (Alexa Fluor® 750)

Codice catalogo: (BOSSBS-15187R-A750)
Fornitore: Bioss
Codice articolo fornitore: BS-15187R-A750
Codice articolo locale: BOSSBS-15187R-A750
Descrizione: C4orf17 (chromosome 4 open reading frame 17) is a 359 amino acid protein encoded by a gene that maps to human chromosome 4. Human chromosome 4 represents approximately 6% of the human genome and contains nearly 900 genes. Notably, the Huntingtin gene, which is found to encode an expanded glutamine tract in cases of Huntington's disease, is on chromosome 4. FGFR-3 is also encoded by a gene that is located on chromosome 4, and has been associated with thanatophoric dwarfism, achondroplasia, Muenke syndrome and bladder cancer. Chromosome 4 is also tied to Ellis-van Creveld syndrome, methylmalonic acidemia and polycystic kidney disease.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-15187R-A350

Anti-C4orf17 Rabbit Polyclonal Antibody (Alexa Fluor® 350)

Codice catalogo: (BOSSBS-15187R-A350)
Fornitore: Bioss
Codice articolo fornitore: BS-15187R-A350
Codice articolo locale: BOSSBS-15187R-A350
Descrizione: C4orf17 (chromosome 4 open reading frame 17) is a 359 amino acid protein encoded by a gene that maps to human chromosome 4. Human chromosome 4 represents approximately 6% of the human genome and contains nearly 900 genes. Notably, the Huntingtin gene, which is found to encode an expanded glutamine tract in cases of Huntington's disease, is on chromosome 4. FGFR-3 is also encoded by a gene that is located on chromosome 4, and has been associated with thanatophoric dwarfism, achondroplasia, Muenke syndrome and bladder cancer. Chromosome 4 is also tied to Ellis-van Creveld syndrome, methylmalonic acidemia and polycystic kidney disease.
UOM: 1 * 100 µl
Image Unavailable-PROOMM0687.00

Azelaic acid

Codice catalogo: (PROOMM0687.00)
Fornitore: LGC Standards PROMOCHEM
Codice articolo fornitore: MM0687.00
Codice articolo locale: PROOMM0687.00
Descrizione: Azelaic acid
UOM: 1 * 500 mg
Image Unavailable-BOSSBS-9203R-CY7

Anti-CD300C Rabbit Polyclonal Antibody (Cy7®)

Codice catalogo: (BOSSBS-9203R-CY7)
Fornitore: Bioss
Codice articolo fornitore: BS-9203R-CY7
Codice articolo locale: BOSSBS-9203R-CY7
Descrizione: CD300C , also known as CLM-6 (CMRF35-like molecule 6), is a 224 amino acid single-pass type I membrane protein that is present on the surface of neutrophils, monocytes and a select proportion of peripheral blood B and T lymphocytes. CD300C contains two potential N-gylcosylation sites, a potential O-glycosylated hinge-like region and an Ig-like V-type (immunoglobulin-like) domain that is very similar to the Fc receptor for polymeric IgA and IgM. The gene encoding CD300C is localized to a region on human chromosome 17 that harbors a susceptilibty locus for psoriasis, dermatitis and rheumatoid arthritis, suggesting a possible involvement of CD300C with these conditions.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-9203R-CY5.5

Anti-CD300C Rabbit Polyclonal Antibody (Cy5.5®)

Codice catalogo: (BOSSBS-9203R-CY5.5)
Fornitore: Bioss
Codice articolo fornitore: BS-9203R-CY5.5
Codice articolo locale: BOSSBS-9203R-CY5.5
Descrizione: CD300C , also known as CLM-6 (CMRF35-like molecule 6), is a 224 amino acid single-pass type I membrane protein that is present on the surface of neutrophils, monocytes and a select proportion of peripheral blood B and T lymphocytes. CD300C contains two potential N-gylcosylation sites, a potential O-glycosylated hinge-like region and an Ig-like V-type (immunoglobulin-like) domain that is very similar to the Fc receptor for polymeric IgA and IgM. The gene encoding CD300C is localized to a region on human chromosome 17 that harbors a susceptilibty locus for psoriasis, dermatitis and rheumatoid arthritis, suggesting a possible involvement of CD300C with these conditions.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-11695R-A488

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

Codice catalogo: (BOSSBS-11695R-A488)
Fornitore: Bioss
Codice articolo fornitore: BS-11695R-A488
Codice articolo locale: BOSSBS-11695R-A488
Descrizione: The 3-HAO family of proteins consists of intramolecular dioxygenases that contain non-heme ferrous iron. HAAO (3-hydroxyanthranilate 3,4-dioxygenase), also known as HAO or 3-HAO, is a 286 amino acid monomeric cytoplasmic protein that belongs to the 3-HAO family. Utilizing Fe2+ ions as a cofactor, HAAO participates in the formation of quinolinic acid (QUIN), and excitotoxin, by catalyzing the oxidative ring opening of 3-hydroxyanthranilate to 2-amino-3-carboxymuconate semialdehyde. HAAO may play a role in disorders that are associated with varying levels of QUIN expression, and is widely expressed in peripheral organs, including kidney and liver. Existing as two alternatively spliced isoforms, the gene encoding HAAO maps to human chromosome 2p21 and mouse chromosome 17 E4.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-11695R-A350

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

Codice catalogo: (BOSSBS-11695R-A350)
Fornitore: Bioss
Codice articolo fornitore: BS-11695R-A350
Codice articolo locale: BOSSBS-11695R-A350
Descrizione: The 3-HAO family of proteins consists of intramolecular dioxygenases that contain non-heme ferrous iron. HAAO (3-hydroxyanthranilate 3,4-dioxygenase), also known as HAO or 3-HAO, is a 286 amino acid monomeric cytoplasmic protein that belongs to the 3-HAO family. Utilizing Fe2+ ions as a cofactor, HAAO participates in the formation of quinolinic acid (QUIN), and excitotoxin, by catalyzing the oxidative ring opening of 3-hydroxyanthranilate to 2-amino-3-carboxymuconate semialdehyde. HAAO may play a role in disorders that are associated with varying levels of QUIN expression, and is widely expressed in peripheral organs, including kidney and liver. Existing as two alternatively spliced isoforms, the gene encoding HAAO maps to human chromosome 2p21 and mouse chromosome 17 E4.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-3239R

Anti-CK17 Rabbit Polyclonal Antibody

Codice catalogo: (BOSSBS-3239R)
Fornitore: Bioss
Codice articolo fornitore: BS-3239R
Codice articolo locale: BOSSBS-3239R
Descrizione: 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].
UOM: 1 * 100 µl
Image Unavailable-TCIAE0853-25G

Ethyl all-cis-5,8,11,14,17-eicosapentaenoate >65.0% (by GC) stabilizzato

Codice catalogo: (TCIAE0853-25G)
Fornitore: TCI
Codice articolo fornitore: E0853-25G
Codice articolo locale: TCIAE0853-25G
Descrizione: Ethyl all-cis-5,8,11,14,17-eicosapentaenoate >65.0% (by GC) stabilizzato
UOM: 1 * 25 g
Product Image-ACRO405195000

Sodium cholate 99%

Fornitore: Thermo Fisher Scientific
Descrizione: Sodium cholate 99%

MSDS Certificati

Image Unavailable-BOSSBS-15187R

Anti-C4orf17 Rabbit Polyclonal Antibody

Codice catalogo: (BOSSBS-15187R)
Fornitore: Bioss
Codice articolo fornitore: BS-15187R
Codice articolo locale: BOSSBS-15187R
Descrizione: C4orf17 (chromosome 4 open reading frame 17) is a 359 amino acid protein encoded by a gene that maps to human chromosome 4. Human chromosome 4 represents approximately 6% of the human genome and contains nearly 900 genes. Notably, the Huntingtin gene, which is found to encode an expanded glutamine tract in cases of Huntington's disease, is on chromosome 4. FGFR-3 is also encoded by a gene that is located on chromosome 4, and has been associated with thanatophoric dwarfism, achondroplasia, Muenke syndrome and bladder cancer. Chromosome 4 is also tied to Ellis-van Creveld syndrome, methylmalonic acidemia and polycystic kidney disease.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-15187R-A555

Anti-C4orf17 Rabbit Polyclonal Antibody (Alexa Fluor® 555)

Codice catalogo: (BOSSBS-15187R-A555)
Fornitore: Bioss
Codice articolo fornitore: BS-15187R-A555
Codice articolo locale: BOSSBS-15187R-A555
Descrizione: C4orf17 (chromosome 4 open reading frame 17) is a 359 amino acid protein encoded by a gene that maps to human chromosome 4. Human chromosome 4 represents approximately 6% of the human genome and contains nearly 900 genes. Notably, the Huntingtin gene, which is found to encode an expanded glutamine tract in cases of Huntington's disease, is on chromosome 4. FGFR-3 is also encoded by a gene that is located on chromosome 4, and has been associated with thanatophoric dwarfism, achondroplasia, Muenke syndrome and bladder cancer. Chromosome 4 is also tied to Ellis-van Creveld syndrome, methylmalonic acidemia and polycystic kidney disease.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-15187R-FITC

Anti-C4orf17 Rabbit Polyclonal Antibody (FITC (Fluorescein Isothiocyanate))

Codice catalogo: (BOSSBS-15187R-FITC)
Fornitore: Bioss
Codice articolo fornitore: BS-15187R-FITC
Codice articolo locale: BOSSBS-15187R-FITC
Descrizione: C4orf17 (chromosome 4 open reading frame 17) is a 359 amino acid protein encoded by a gene that maps to human chromosome 4. Human chromosome 4 represents approximately 6% of the human genome and contains nearly 900 genes. Notably, the Huntingtin gene, which is found to encode an expanded glutamine tract in cases of Huntington's disease, is on chromosome 4. FGFR-3 is also encoded by a gene that is located on chromosome 4, and has been associated with thanatophoric dwarfism, achondroplasia, Muenke syndrome and bladder cancer. Chromosome 4 is also tied to Ellis-van Creveld syndrome, methylmalonic acidemia and polycystic kidney disease.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-11695R-A680

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

Codice catalogo: (BOSSBS-11695R-A680)
Fornitore: Bioss
Codice articolo fornitore: BS-11695R-A680
Codice articolo locale: BOSSBS-11695R-A680
Descrizione: The 3-HAO family of proteins consists of intramolecular dioxygenases that contain non-heme ferrous iron. HAAO (3-hydroxyanthranilate 3,4-dioxygenase), also known as HAO or 3-HAO, is a 286 amino acid monomeric cytoplasmic protein that belongs to the 3-HAO family. Utilizing Fe²⁺ ions as a cofactor, HAAO participates in the formation of quinolinic acid (QUIN), and excitotoxin, by catalyzing the oxidative ring opening of 3-hydroxyanthranilate to 2-amino-3-carboxymuconate semialdehyde. HAAO may play a role in disorders that are associated with varying levels of QUIN expression, and is widely expressed in peripheral organs, including kidney and liver. Existing as two alternatively spliced isoforms, the gene encoding HAAO maps to human chromosome 2p21 and mouse chromosome 17 E4.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-11904R-A750

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

Codice catalogo: (BOSSBS-11904R-A750)
Fornitore: Bioss
Codice articolo fornitore: BS-11904R-A750
Codice articolo locale: BOSSBS-11904R-A750
Descrizione: Notum is a 496 amino acid secreted protein that belongs to the pectinacetylesterase family and may deacetylate GlcNAc residues on cell surface glycans. The gene that encodes Notum consists of approximately 9334 bases and maps to human chromosome 17q25.3. Encoding more than 1200 genes, chromosome 17 comprises over 2.5% of the human genome. Two key tumour suppressor genes are associated with chromosome 17, namely, p53 and BRCA1. tumour 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, though specifically it is recognised as a genetic determinant of early onset breast cancer and predisposition to cancers of ovary, colon, prostate gland and fallopian tubes.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-9289R-CY7

Anti-PACRG Rabbit Polyclonal Antibody (Cy7®)

Codice catalogo: (BOSSBS-9289R-CY7)
Fornitore: Bioss
Codice articolo fornitore: BS-9289R-CY7
Codice articolo locale: BOSSBS-9289R-CY7
Descrizione: The deduced 257 amino acid protein PACRG (Parkin co-regulated gene) shows potential links to the ubiquitin/proteasome system. PACRG and Parkin are attached in a head-to-head arrangement on opposite DNA strands and share a common 5' flanking promoter region. The PACRG gene maps to chromosome 6q26; Northern blot analysis detects PACRG expression in all tissues examined except placenta. Using a positional cloning strategy in 197 Vietnamese leprosy simplex families (i.e. families with two unaffected parents and one affected child), significant connections between leprosy and 17 markers in the 5' regulatory region that PARK2 and PACRG share were observed. Possession of two or more of the 17 risk alleles is highly predictive of leprosy.PACRG is a gene located very close to parkin, in reverse orientation on the chromosome. It is thought to be co-transcribed with parkin by a bi-directional promoter between the two genes.
UOM: 1 * 100 µl
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