N-Methyl-2-brom-4-chloranilin+Hydrochlorid
Artikel-Nr:
(253300-10)
Lieferant:
Merck Millipore (Calbiochem)
Hersteller-Artikelnummer::
253300-10
Lokale Artikelnummer::
CALB253300-10
Beschreibung:
Deltamethrin is a synthetic type II pyrethroid that acts as a potent inhibitor of calcineurin (protein phosphatase 2B; IC50 = 100 pM). Also have varied effects on ion channels. Causes an increase in neurotransmitter release at synapses, and increases intrasynaptosomal Ca<sup>2+</sup> levels.
VE:
1 * 10 mg
Lieferant:
Novabiochem (Part of Merck)
Beschreibung:
It is a bifunctional 20 atom PEG spacer. It can be introduced using standard coupling methods, such as PyBOP®, HBTU or TBTU and is compatible with standard TFA cleavage protocols.
Artikel-Nr:
(PIER88261)
Lieferant:
Thermo Scientific
Hersteller-Artikelnummer::
88261
Lokale Artikelnummer::
PIER88261
Beschreibung:
96-well deep-well plate, PP, 2,2 ml, suitable for 96-well microdialysis devices, Pierce
VE:
1 * 1 ST
Artikel-Nr:
(BOCH5670)
Lieferant:
BOCHEM
Hersteller-Artikelnummer::
5670
Lokale Artikelnummer::
BOCH5670
Beschreibung:
These bossheads are ideal for supporting overhead stirrers.
VE:
1 * 1 ST
Artikel-Nr:
(818-0132)
Lieferant:
Texwipe
Hersteller-Artikelnummer::
TX5811
Lokale Artikelnummer::
TEXWTX5811
Beschreibung:
TexWrite® 22, latex-saturated cellulose cleanroom documentation sheets without organic fillers.
VE:
1 * 2.500 ST
Artikel-Nr:
(PROOCIL-PCB-208-CS)
Lieferant:
LGC Standards PROMOCHEM
Hersteller-Artikelnummer::
CIL-PCB-208-CS
Lokale Artikelnummer::
PROOCIL-PCB-208-CS
Beschreibung:
Organic Standard, 2,2',3,3',4,5,5',6,6'-Nonachlorbiphenyl (PCB Nr. 208) 100 µg/ml in Isooctan, Packung: Glasflasche
VE:
1 * 1,2 mL
Lieferant:
HAMILTON BONADUZ
Beschreibung:
Spritzen, Chromatographie, Microliter™, HPLC/GC, 1001 LTNCH, Volumen: 1 µl, Gauge: 22, Länge: 51 mm, VE: 1
Artikel-Nr:
(BOSSBS-9748R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9748R
Lokale Artikelnummer::
BOSSBS-9748R
Beschreibung:
Ankyrins are membrane adaptor molecules that play important roles in coupling integral membrane proteins to the spectrin-based cytoskeleton network. Mutations of ankyrin genes lead to severe genetic diseases, such as fatal cardiac arrhythmias and hereditary spherocytosis. ANKRD22 (ankyrin repeat domain 22) is a 191 amino acid protein that contains four ANK repeats. Conserved in chimpanzee, dog, cow, mouse, rat, chicken and zebrafish, ANKRD22 is encoded by a gene that maps to human chromosome 10. Chromosome 10 encodes nearly 1,200 genes within 135 million bases, making up approximately 4.5% of the human genome. Several protein-coding genes, including those that encode for chemokines, cadherins, excision repair proteins, early growth response factors (Egrs) and fibroblast growth receptors (FGFRs), are located on chromosome 10. Defects in genes that map to chromosome 10 are associated with Charcot-Marie Tooth disease, Jackson-Weiss syndrome, Usher syndrome, nonsyndromatic deafness, Wolman’s syndrome, Cowden syndrome, multiple endocrine neoplasia type 2 and porphyria.
VE:
1 * 100 µl
Lieferant:
Sigma-Aldrich
Beschreibung:
BIS-TRIS-Propan, Sigma-Aldrich®
Artikel-Nr:
(BOSSBS-12330R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12330R-A750
Lokale Artikelnummer::
BOSSBS-12330R-A750
Beschreibung:
The tripartite motif (TRIM) family of proteins are characterised by a conserved TRIM domain that includes a coiled-coil region, a B-box type zinc finger, one RING finger and three zinc-binding domains. Staf-50 (50 kDa-stimulated trans-acting factor), also known as TRIM22 (tripartite motif-containing 22), RNF94 or GPSTAF50, is a 498 amino acid cytoplasmic protein that belongs to the TRIM family and, characteristic of TRIM family members, contains one RING-type zinc finger, one B box-type zinc finger and one SPRY domain. Induced by IFN-å and IFN-, Staf-50 is strongly expressed in ovary, spleen, thymus and peripheral blood leukocytes where it is thought to mediate the antiviral effects of IFN proteins. Additionally, Staf-50 is present in leukemic cells, suggesting a role in cancer formation and metastasis. Staf-50 exists as two alternatively spliced isoforms which are encoded by a gene that maps to human chromosome 11.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9492R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9492R
Lokale Artikelnummer::
BOSSBS-9492R
Beschreibung:
C9orf4 is a 344 amino acid single-pass membrane protein that is primarily expressed in adult and fetal brain and is weakly expressed in spinal cord, adult ovary and medulla. C9orf4 contains one DOMON domain, a predominantly β-sheet domain that is thought to aide in extracellular adhesion. The gene encoding C9orf4 maps to human chromosome 9, which consists of about 145 million bases and 4% of the human genome and encodes nearly 900 genes. Considered to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias.
VE:
1 * 100 µl
Artikel-Nr:
(USBI032430-BIOTIN)
Lieferant:
US Biological
Hersteller-Artikelnummer::
032430-BIOTIN
Lokale Artikelnummer::
USBI032430-BIOTIN
Beschreibung:
Anti-BASP1 Rabbit Polyclonal Antibody (Biotin)
VE:
1 * 200 µl
Lieferant:
MP Biomedicals
Beschreibung:
Chymostatin ([(S)-1-Carboxy-2-phenylethyl]-carbamoyl-α-[2-iminohexahydro-4(S)-pyrimidyl]-(S)-Gly-X-Phe-al) Source/Species: Microbial A mixture of type A, B, and C. X = Leu (Type A); Ile (Type B); Val (Type C). Ref: 1. Umezawa, H., et al., J. Antibiot., 23: 425 (1970). 2. Tatsuta, K., et al., J. Antibiot., 26: 625 (1973).
Artikel-Nr:
(BOSSBS-8594R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8594R
Lokale Artikelnummer::
BOSSBS-8594R
Beschreibung:
Ankyrins are membrane adaptor molecules that play important roles in coupling integral membrane proteins to the spectrin-based cytoskeleton network. Mutations of ankyrin genes lead to severe genetic diseases, such as fatal cardiac arrhythmias and hereditary spherocytosis. ANKRD22 (ankyrin repeat domain 22) is a 191 amino acid protein that contains four ANK repeats. Conserved in chimpanzee, dog, cow, mouse, rat, chicken and zebrafish, ANKRD22 is encoded by a gene that maps to human chromosome 10. Chromosome 10 encodes nearly 1,200 genes within 135 million bases, making up approximately 4.5% of the human genome. Several protein-coding genes, including those that encode for chemokines, cadherins, excision repair proteins, early growth response factors (Egrs) and fibroblast growth receptors (FGFRs), are located on chromosome 10. Defects in genes that map to chromosome 10 are associated with Charcot-Marie Tooth disease, Jackson-Weiss syndrome, Usher syndrome, nonsyndromatic deafness, Wolman’s syndrome, Cowden syndrome, multiple endocrine neoplasia type 2 and porphyria.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8594R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8594R-A647
Lokale Artikelnummer::
BOSSBS-8594R-A647
Beschreibung:
Ankyrins are membrane adaptor molecules that play important roles in coupling integral membrane proteins to the spectrin-based cytoskeleton network. Mutations of ankyrin genes lead to severe genetic diseases, such as fatal cardiac arrhythmias and hereditary spherocytosis. ANKRD22 (ankyrin repeat domain 22) is a 191 amino acid protein that contains four ANK repeats. Conserved in chimpanzee, dog, cow, mouse, rat, chicken and zebrafish, ANKRD22 is encoded by a gene that maps to human chromosome 10. Chromosome 10 encodes nearly 1,200 genes within 135 million bases, making up approximately 4.5% of the human genome. Several protein-coding genes, including those that encode for chemokines, cadherins, excision repair proteins, early growth response factors (Egrs) and fibroblast growth receptors (FGFRs), are located on chromosome 10. Defects in genes that map to chromosome 10 are associated with Charcot-Marie Tooth disease, Jackson-Weiss syndrome, Usher syndrome, nonsyndromatic deafness, Wolman’s syndrome, Cowden syndrome, multiple endocrine neoplasia type 2 and porphyria.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8594R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8594R-CY3
Lokale Artikelnummer::
BOSSBS-8594R-CY3
Beschreibung:
Ankyrins are membrane adaptor molecules that play important roles in coupling integral membrane proteins to the spectrin-based cytoskeleton network. Mutations of ankyrin genes lead to severe genetic diseases, such as fatal cardiac arrhythmias and hereditary spherocytosis. ANKRD22 (ankyrin repeat domain 22) is a 191 amino acid protein that contains four ANK repeats. Conserved in chimpanzee, dog, cow, mouse, rat, chicken and zebrafish, ANKRD22 is encoded by a gene that maps to human chromosome 10. Chromosome 10 encodes nearly 1,200 genes within 135 million bases, making up approximately 4.5% of the human genome. Several protein-coding genes, including those that encode for chemokines, cadherins, excision repair proteins, early growth response factors (Egrs) and fibroblast growth receptors (FGFRs), are located on chromosome 10. Defects in genes that map to chromosome 10 are associated with Charcot-Marie Tooth disease, Jackson-Weiss syndrome, Usher syndrome, nonsyndromatic deafness, Wolman’s syndrome, Cowden syndrome, multiple endocrine neoplasia type 2 and porphyria.
VE:
1 * 100 µl
Preis auf Anfrage
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