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2\'-Methoxy-3\'-methylbiphenyl-3-carbons\u00E4ure
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2\'-Methoxy-3\'-methylbiphenyl-3-carbons\u00E4ure
Artikel-Nr:
(MOLE17439999-25G)
Lieferant:
Molekula
Hersteller-Artikelnummer::
17439999-25G
Lokale Artikelnummer::
MOLE17439999-25G
Beschreibung:
3-Amino-2-chlorpyridin
VE:
1 * 25 g
 This is a MarketSource item. Additional charges may apply
Artikel-Nr:
(FLUO012728-5G)
Lieferant:
FLUOROCHEM
Hersteller-Artikelnummer::
012728-5G
Lokale Artikelnummer::
FLUO012728-5G
Beschreibung:
2-Amino-6-chlorpyridin
VE:
1 * 5 g
This is a MarketSource item. Additional charges may apply
Artikel-Nr:
(BLDPBD20273-10G)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD20273-10G
Lokale Artikelnummer::
BLDPBD20273-10G
Beschreibung:
2,2'-({4-[(2-Hydroxyethyl)amino]-3-nitrophenyl}imino)diethanol 97%
VE:
1 * 10 g
Lieferant:
Thermo Scientific
Beschreibung:
Taurodeoxycholic acid sodium salt hydrate 97%
Artikel-Nr:
(FLUO010687-5G)
Lieferant:
FLUOROCHEM
Hersteller-Artikelnummer::
010687-5G
Lokale Artikelnummer::
FLUO010687-5G
Beschreibung:
5-Amino-2-methylbenzotrifluorid
VE:
1 * 5 g
This is a MarketSource item. Additional charges may apply
Lieferant:
Thermo Scientific
Beschreibung:
2-Amino-3-thiophencarbonitril
Artikel-Nr:
(MOLEM58220382)
Lieferant:
Molekula
Hersteller-Artikelnummer::
M58220382
Lokale Artikelnummer::
MOLEM58220382
Beschreibung:
(S)-(+)-2-Amino-1-propanol
VE:
1 * 5 g
This is a MarketSource item. Additional charges may apply
Artikel-Nr:
(BOSSBS-15078R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15078R-A647
Lokale Artikelnummer::
BOSSBS-15078R-A647
Beschreibung:
C1orf85, also known as Lysosomal protein NCU-G1, is a 406 amino acid single-pass membrane protein that is highly glycosylated on its amino-terminal end. Transcription of the gene encoding C1orf85 is activated by TFEB, a transcription factor that specifically recognizes and binds E-box sequences. There are two isoforms of C1orf85 that are produced as a result of alternative splicing events. The C1orf85 maps to human chromosome 1, the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1.
VE:
1 * 100 µl
Artikel-Nr:
(FLUO010658-25G)
Lieferant:
FLUOROCHEM
Hersteller-Artikelnummer::
010658-25G
Lokale Artikelnummer::
FLUO010658-25G
Beschreibung:
3-Amino-2-naphthoesäure
VE:
1 * 25 g
This is a MarketSource item. Additional charges may apply
Lieferant:
Thermo Scientific
Beschreibung:
2-Amino-4-ethylpyridin
Lieferant:
Thermo Scientific
Beschreibung:
4-Amino-o-anissäure
Lieferant:
Sigma-Aldrich
Beschreibung:
4-Amino-m-kresol, Sigma-Aldrich®
Artikel-Nr:
(BOSSBS-13138R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13138R-A750
Lokale Artikelnummer::
BOSSBS-13138R-A750
Beschreibung:
Fanconi anemia (FA) is an autosomal recessive disorder characterized by bone marrow failure, birth defects and chromosomal instability. At the cellular level, FA is characterized by spontaneous chromosomal breakage and a unique hypersensitivity to DNA cross-linking agents. At least eight complementation groups (A-G) have been identified and six FA genes (for subtypes A, C, D2, E, F and G) have been cloned. The FA proteins lack sequence homologies or motifs that could point to a molecular function. The cellular accumulation of FA proteins, including FANCA and FANCG, is subject to regulation by TNF alpha signaling. Phosphorylation of FANC (Fanconi anemia complementation group) proteins is thought to be important for the function of the FA pathway. FANCA, also known as FACA and FANCH, associates with the Brm-related gene 1 (BRG1) product, a subunit of the SWI/SNF complex which remodels chromatin structure through a DNA-dependent ATPase activity. FANCA is mainly expressed in lymphoid tissues, testis and ovary. The amino-terminal region of the FANCA protein is required for FANCG binding, FANCC binding, nuclear localization and functional activity of the complex. The human FANCA gene maps to chromosome 16q24.3 and encodes a 1,455 amino acid protein.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8341R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8341R-CY7
Lokale Artikelnummer::
BOSSBS-8341R-CY7
Beschreibung:
CPXM (carboxypeptidase X, member 1) belongs to the peptidase M14 family. However, no carboxypeptidase activity has yet been detected. It may be involved in cell-cell interactions.Members of the M14 metallocarboxypeptidase protein family serve many diverse functions and are divided into three subfamilies based on structure, function and amino acid sequence similarity. Belonging to the N/E subfamily, CPXM (metallocarboxypeptidase CPX-1) is a 734 amino acid protein that contains a F5/8 type C domain and likely binds one zinc ion per subunit. Most members of the N/E subfamily contain several domains, including an active carboxypeptidase domain and signal peptide, and are thought to function mostly in protein-protein interactions and/or protein-membrane interactions, thereby targeting the protein to specific locations within the secretory pathway. CPXM is a unique member of this subfamily in that it does not appear to exhibit any enzymatic activity due to lack of several active-site residues that are present in the catalytic domain of other members of the N/E subfamily. Studies showing that CPXM expression is regulated during osteoclastogenesis suggest that CPXM may play a role in osteoclast differentiation. There are two isoforms of CPXM which are a result of alternative splicing events.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-15486R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15486R-CY5
Lokale Artikelnummer::
BOSSBS-15486R-CY5
Beschreibung:
Zinc-finger proteins contain DNA-binding domains and have a wide variety of functions, most of which encompass some form of transcriptional activation or repression. The majority of Zinc-finger proteins contain a Kr_ppel-type DNA binding domain and a KRAB domain, which is thought to interact with KAP1, thereby recruiting histone modifying proteins. HIC-2 (hypermethylated in cancer 2) possesses Zinc finger motifs that are thought to be important for DNA-binding and also has a BTB/POZ domain at the N-terminus, which is thought to be important for protein-protein binding, as well as for the binding of transcription factors. HIC-2 is also known as Hic-3, HIC1-related gene on chromosome 22 or Zinc finger and BTB domain-containing protein 30, and is a 615 amino acid protein that is expressed as two isoforms produced by alternative splicing. HIC-2 is highly expressed in cerebellum and is localised to the nucleus in cells. HIC-2 contains a short amino acid sequence that is thought to interact with CtBP, a transcriptional repressor. The gene sequence associated with HIC-2 is thought to be a target for miRNAs (microRNAs) which are expressed in many cancers, suggesting that HIC-2 could possess tumor suppressor capabilities.
VE:
1 * 100 µl
Artikel-Nr:
(CHMPFL13399.POR)
Lieferant:
CHEMPUR
Hersteller-Artikelnummer::
FL13399.POR
Lokale Artikelnummer::
CHMPFL13399.POR
Beschreibung:
2-Amino-4-chlorbenzothiazol
VE:
1 * 1 ST
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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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