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4\\\\\\\'-Chlorbiphenyl-3-carbons\\\\u00E4ure
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4\\\\\\\'-Chlorbiphenyl-3-carbons\\\\u00E4ure
Artikel-Nr:
(BOSSBS-11381R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11381R-CY3
Lokale Artikelnummer::
BOSSBS-11381R-CY3
Beschreibung:
Contributes to degradation of proteins cross-linked by transglutaminases. Degrades the cross-link between a lysine and a glutamic acid residue from two proteins that have been cross-linked by transglutaminases. Catalyzes the formation of 5-oxoproline from L-gamma-glutamyl-L-epsilon-lysine. Inactive with L-gamma-glutamyl-alpha-amino acid substrates such as L-gamma-glutamyl-L-alpha-cysteine and L-gamma-glutamyl-L-alpha-alanine.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-1603R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-1603R-FITC
Lokale Artikelnummer::
BOSSBS-1603R-FITC
Beschreibung:
The protein encoded by this gene belongs to the class-II aminoacyl-tRNA synthetase family. Aminoacyl-tRNA synthetases play critical roles in mRNA translation by charging tRNAs with their cognate amino acids. The encoded protein is a mitochondrial enzyme that specifically aminoacylates alanyl-tRNA. Mutations in this gene are a cause of combined oxidative phosphorylation deficiency 8.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-6170R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-6170R-A488
Lokale Artikelnummer::
BOSSBS-6170R-A488
Beschreibung:
RALA, resorcylic acid lactone alpha, is a low molecular weight GTP binding protein belonging to the RAS family of onco proteins. RALA has a 50% amino acid homology with RAS and an 85% homology with RALB. GTP binding proteins mediate the transmembrane signaling initiated by the occupancy of certain cell surface receptors.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9089R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9089R-A680
Lokale Artikelnummer::
BOSSBS-9089R-A680
Beschreibung:
Members of the F-box protein family, such as FBXO27, are characterised by an approximately 40-amino acid F-box motif. SCF complexes, formed by SKP1, cullin (CUL1), and F-box proteins, act as protein-ubiquitin ligases. F-box proteins interact with SKP1 through the F box, and they interact with ubiquitination targets through other protein interaction domains.
VE:
1 * 100 µl
Artikel-Nr:
(BSENR-1493-50)
Lieferant:
Biosensis
Hersteller-Artikelnummer::
R-1493-50
Lokale Artikelnummer::
BSENR-1493-50
Beschreibung:
Human beta-Lipotropin is a 93 amino acid polypeptide that is cleaved from carboxy-terminal fragment of the precursor pro-opiomelanocortin (POMC). It stimulates melanocytes to produce melanin, and can also be cleaved into smaller peptides including opioid peptides: gamma-lipotropin, alpha-MSH, beta-MSH, gamma-MSH, alpha-endorphin, beta-endorphin, gamma-endorphin and met-enkephalin
VE:
1 * 50 µG
Artikel-Nr:
(BOSSBS-5813R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-5813R-FITC
Lokale Artikelnummer::
BOSSBS-5813R-FITC
Beschreibung:
Proline oxidase catalyzes the conversion of proline to pyrroline-5-carboxylate, or P5C during the degradation of the amino acid Proline. Defects in PRODH are the cause of hyperprolinemia type 1, a disorder characterized by elevated serum proline levels. Defective PRODH may be involved in the psychiatric and behavioral phenotypes associated with the 22q11 velocardiofacial and DiGeorge syndrome and may be associated with susceptibility to schizophrenia 4 (SCZD4).
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-5813R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-5813R-A750
Lokale Artikelnummer::
BOSSBS-5813R-A750
Beschreibung:
Proline oxidase catalyses the conversion of proline to pyrroline-5-carboxylate, or P5C during the degradation of the amino acid Proline. Defects in PRODH are the cause of hyperprolinemia type 1, a disorder characterised by elevated serum proline levels. Defective PRODH may be involved in the psychiatric and behavioral phenotypes associated with the 22q11 velocardiofacial and DiGeorge syndrome and may be associated with susceptibility to schizophrenia 4 (SCZD4).
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-5813R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-5813R-A680
Lokale Artikelnummer::
BOSSBS-5813R-A680
Beschreibung:
Proline oxidase catalyses the conversion of proline to pyrroline-5-carboxylate, or P5C during the degradation of the amino acid Proline. Defects in PRODH are the cause of hyperprolinemia type 1, a disorder characterised by elevated serum proline levels. Defective PRODH may be involved in the psychiatric and behavioral phenotypes associated with the 22q11 velocardiofacial and DiGeorge syndrome and may be associated with susceptibility to schizophrenia 4 (SCZD4).
VE:
1 * 100 µl
Lieferant:
Avantor
Beschreibung:
Glycin (H-Gly-OH) ≥99,5% (Trockenmasse), ultrareines Bioreagenz for Electrophoresis, Liquid Chromatography and Molecular Biology, für die Flüssigchromatographie, J.T.Baker®
Artikel-Nr:
(BOSSBS-0136R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-0136R-CY3
Lokale Artikelnummer::
BOSSBS-0136R-CY3
Beschreibung:
GTP cyclohydrolase I (also designated dopa-responsive dystonia) catalyzes the conversion of GTP to D-erythro-7,8-dihydroneopterin triphosphate, the first and rate-limiting step in tetrahydrobiopterin (BH4) biosynthesis. Tetrahydrobiopterin is an essential cofactor for 3 aromatic amino acid monooxygenases: phenylalanine, tyrosine, and tryptophan hydroxylases. Animals can synthesize tetrahydrobiopterin in vivo from GTP through several enzymatic reactions.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-0136R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-0136R
Lokale Artikelnummer::
BOSSBS-0136R
Beschreibung:
GTP cyclohydrolase I (also designated dopa-responsive dystonia) catalyzes the conversion of GTP to D-erythro-7,8-dihydroneopterin triphosphate, the first and rate-limiting step in tetrahydrobiopterin (BH4) biosynthesis. Tetrahydrobiopterin is an essential cofactor for 3 aromatic amino acid monooxygenases: phenylalanine, tyrosine, and tryptophan hydroxylases. Animals can synthesize tetrahydrobiopterin in vivo from GTP through several enzymatic reactions.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11825R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11825R-CY3
Lokale Artikelnummer::
BOSSBS-11825R-CY3
Beschreibung:
DOCK 7 is a 2,140 amino acid protein that localizes to developing axons and contains one DHR-1 domain and one DHR-2 domain. Expressed in a variety of tissues, DOCK 7 functions as a guanine nucleotide exchange factor (GEF) that specifically activates Rac 1 and Rac 3 by catalyzing the exchange of bound GDP for free GTP. Multiple isoforms of DOCK 7 exist due to alternative splicing events.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-2526R-CY5.5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-2526R-CY5.5
Lokale Artikelnummer::
BOSSBS-2526R-CY5.5
Beschreibung:
CD160, a 27 kDa glycoprotein, was initially identified with the monoclonal antibody BY55. Its expression is tightly associated with peripheral blood NK cells and CD8 T lymphocytes with cytolytic effector activity. The cDNA sequence of CD160 predicts a cysteine rich, glycosylphosphatidylinositol anchored protein of 181 amino acids with a single Ig-like domain weakly homologous to KIR2DL4 molecule.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8240R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8240R-HRP
Lokale Artikelnummer::
BOSSBS-8240R-HRP
Beschreibung:
FERM domains are roughly 150 amino acids in length and are found in a number of cytoskeletal-associated proteins such as Ezrin, Radixin, Moesin and 4.1 (erythrocyte membrane protein band 4.1), where they provide a link between cytoskeletal signals and membrane dynamics. FRMD8 (FERM domain-containing protein 8), also known as FKSG44, is a 464 amino acid protein containing one FERM domain. Existing as two alternatively spliced isoforms, the gene encoding FRMD8 maps to human chromosome 11q13.1. With approximately 135 million base pairs and 1,400 genes, chromosome 11 makes up around 4% of human genomic DNA and is considered a gene and disease association dense chromosome. Wilms' tumors, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9394R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9394R-A647
Lokale Artikelnummer::
BOSSBS-9394R-A647
Beschreibung:
WD-repeats are motifs that are found in a variety of proteins and are characterized by a conserved core of 40-60 amino acids that commonly form a tertiary propeller structure. While proteins that contain WD-repeats participate in a wide range of cellular functions, they are generally involved in regulatory mechanisms concerning chromatin assembly, cell cycle control, signal transduction, RNA processing, apoptosis and vesicular trafficking. WDR40A (WD-repeat-containing protein 40A), also known as DDB1- CUL4-associated factor 12, is a 453 amino acid cytoplasmic protein that contains four WD-repeats. WDR40A is highly expressed in some cancer cell lines, lung cancer tissues and normal testis. A probable substrate receptor for CUL4-DDB1 E3 ubiquitin-protein ligase complex, WRD40A is suggested to interact with DDB1. WDR40A is encoded by a gene mapping to human chromosome 9p13.3. Human chromosome 9 houses over 900 genes and comprises nearly 4% of the human genome.
VE:
1 * 100 µl
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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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