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2-(Carboxymethyl)-6-fluorobenzoic+acid
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2-(Carboxymethyl)-6-fluorobenzoic+acid
Artikel-Nr:
(BLDPBD145352-250MG)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD145352-250MG
Lokale Artikelnummer::
BLDPBD145352-250MG
Beschreibung:
3,6,9,12,15-Pentaoxatricosan-1-ol 95%
VE:
1 * 250 mg
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
4-Brom-2-(4-morpholino)pyridin 98%
Artikel-Nr:
(BOSSBS-6798R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-6798R-A647
Lokale Artikelnummer::
BOSSBS-6798R-A647
Beschreibung:
Calpains are a family of cytosolic calcium activated cysteine proteases involved in a variety of cellular processes including apoptosis, cell division, modulation of integrin and cytoskeletal interactions, and synaptic plasticity. Calpain 12 was first described in the mouse, most strongly in the skin, and maps to mouse chromosome 7. Isoforms differ in the carboxyterminal ends, ending with aberrant domain III and lacking domain IV. Domains in the large subunit include the amino terminal domain I, the proteinase domain II, domain III, and the EF hand domain IV, making Calpain 12 most similar to calpains 1 and 2.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11736R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11736R
Lokale Artikelnummer::
BOSSBS-11736R
Beschreibung:
NPC2 is a secreted protein mapping against gene 14q24.3 (1,2). NPC2 regulates the lipid composition of sperm membranes during maturation in the epididymis(1,2). Mutations in the NPC2 gene may cause Nieman-Pick type C2 disease and frontal lobe atrophy (1,2,3). Nieman-Pick type C2 is a fatal hereditary disease characterized by defective lysosome release of cholesterol (3). The disease is caused by HE1 deficiency, a lysosmal protein proven to be undetectable in fibroblasts from NPC2 patients (3). This differentiates NPC2 from NPC1, as NPC1 has HE1 protein present (3).
VE:
1 * 100 µl
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
L(+)-Ascorbinsäure ≥99,5%
Lieferant:
Alfa Aesar
Beschreibung:
Niob(V)chlorid ≥99,9% (Metall-Basis)
Artikel-Nr:
(USBI041450)
Lieferant:
US Biological
Hersteller-Artikelnummer::
041450
Lokale Artikelnummer::
USBI041450
Beschreibung:
Anti-SCARB1 Rabbit Polyclonal Antibody
VE:
1 * 200 µl
Artikel-Nr:
(BOSSBS-0019R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-0019R-HRP
Lokale Artikelnummer::
BOSSBS-0019R-HRP
Beschreibung:
Acts as a cytokine involved in enhancing production of interferon-gamma and interleukin-12 and reducing production of interleukin-10 and is essential in the pathway that leads to type I immunity (By similarity).
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-0019R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-0019R-FITC
Lokale Artikelnummer::
BOSSBS-0019R-FITC
Beschreibung:
Acts as a cytokine involved in enhancing production of interferon-gamma and interleukin-12 and reducing production of interleukin-10 and is essential in the pathway that leads to type I immunity (By similarity).
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-3842R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-3842R-A647
Lokale Artikelnummer::
BOSSBS-3842R-A647
Beschreibung:
EIF3S3 binds to the 40S ribosome and promotes the binding of methionyl-tRNAi and mRNA. It associates with the p170 subunit of EIF3. The EIF3 is composed of at least 12 different subunits.
VE:
1 * 100 µl
Lieferant:
Alfa Aesar
Beschreibung:
Vanadium(III)fluorid ≥98%
Lieferant:
Spectrum Chemical
Beschreibung:
Form: Powder
Artikel-Nr:
(BOSSBS-11945R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11945R-HRP
Lokale Artikelnummer::
BOSSBS-11945R-HRP
Beschreibung:
Encoding over 1,100 genes within 132 million bases, chromosome 12 makes up about 4.5% of the human genome. A number of skeletal deformities are linked to chromosome 12 including hypochondrogenesis, achondrogenesis and Kniest dysplasia. Noonan syndrome, which includes heart and facial developmental defects among the primary symptoms, is caused by a mutant form of PTPN11 gene product, SH-PTP2. Chromosome 12 is also home to a homeobox gene cluster which encodes crucial transcription factors for morphogenesis, and the natural killer complex gene cluster encoding C-type lectin proteins which mediate the NK cell response to MHC I interaction. Trisomy 12p leads to facial development defects, seizure disorders and a host of other symptoms varying in severity depending on the extent of mosaicism and is most severe in cases of complete trisomy. The C12orf52 gene product has been provisionally designated C12orf52 pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9948R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9948R-A680
Lokale Artikelnummer::
BOSSBS-9948R-A680
Beschreibung:
Encoding over 1100 genes within 132 million bases, chromosome 12 makes up about 4.5% of the human genome. A number of skeletal deformities are linked to chromosome 12 including hypochondrogenesis, achondrogenesis and Kniest dysplasia. Noonan syndrome, which includes heart and facial developmental defects among the primary symptoms, is caused by a mutant form of PTPN11 gene product, SH-PTP2. Chromosome 12 is also home to a homeobox gene cluster which encodes crucial transcription factors for morphogenesis, and the natural killer complex gene cluster encoding C-type lectin proteins which mediate the NK cell response to MHC I interaction. Trisomy 12p leads to facial development defects, seizure disorders and a host of other symptoms varying in severity depending on the extent of mosaicism and is most severe in cases of complete trisomy. The C12orf42 gene product has been provisionally designated C12orf42 pending further characterisation.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8229R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8229R-A350
Lokale Artikelnummer::
BOSSBS-8229R-A350
Beschreibung:
Encoding over 1,100 genes within 132 million bases, chromosome 12 makes up about 4.5% of the human genome. A number of skeletal deformities are linked to chromosome 12 including hypochondrogenesis, achondrogenesis and Kniest dysplasia. Noonan syndrome, which includes heart and facial developmental defects among the primary symptoms, is caused by a mutant form of PTPN11 gene product, SH-PTP2. Chromosome 12 is also home to a homeobox gene cluster which encodes crucial transcription factors for morphogenesis, and the natural killer complex gene cluster encoding C-type lectin proteins which mediate the NK cell response to MHC I interaction. Trisomy 12p leads to facial development defects, seizure disorders and a host of other symptoms varying in severity depending on the extent of mosaicism and is most severe in cases of complete trisomy. The FAM101A gene product has been provisionally designated FAM101A pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9946R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9946R-A750
Lokale Artikelnummer::
BOSSBS-9946R-A750
Beschreibung:
Encoding over 1100 genes within 132 million bases, chromosome 12 makes up about 4.5% of the human genome. A number of skeletal deformities are linked to chromosome 12 including hypochondrogenesis, achondrogenesis and Kniest dysplasia. Noonan syndrome, which includes heart and facial developmental defects among the primary symptoms, is caused by a mutant form of PTPN11 gene product, SH-PTP2. Chromosome 12 is also home to a homeobox gene cluster which encodes crucial transcription factors for morphogenesis, and the natural killer complex gene cluster encoding C-type lectin proteins which mediate the NK cell response to MHC I interaction. Trisomy 12p leads to facial development defects, seizure disorders and a host of other symptoms varying in severity depending on the extent of mosaicism and is most severe in cases of complete trisomy. The C12orf29 gene product has been provisionally designated C12orf29 pending further characterisation.
VE:
1 * 100 µl
Preis auf Anfrage
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 noch angezeigt wird und Sie Hilfe benötigen, rufen Sie uns an 1-800-932 - 5000.
Lager für diesen Artikel ist begrenzt, kann aber in einem Lagerhaus in Ihrer Nähe zur Verfügung. Bitte stellen Sie sicher, dass Sie in sind angemeldet auf dieser Seite, so dass verfügbare Bestand angezeigt werden können. Wenn das
noch angezeigt wird und Sie Hilfe benötigen, rufen Sie uns an 1-800-932 - 5000.
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