2-(Tributylstannyl)thiazol
Artikel-Nr:
(USBI044078-BIOTIN)
Lieferant:
US Biological
Hersteller-Artikelnummer::
044078-BIOTIN
Lokale Artikelnummer::
USBI044078-BIOTIN
Beschreibung:
Anti-ZFYVE16 Rabbit Polyclonal Antibody (Biotin)
VE:
1 * 200 µl
Lieferant:
Bernd Kraft
Beschreibung:
Salzsäure 16 - 17%, technische Qualität für die Regeneration von Wasservollentsalzungsanlagen
Artikel-Nr:
(MOTI1101001402731)
Lieferant:
MOTIC
Hersteller-Artikelnummer::
1101001402731
Lokale Artikelnummer::
MOTI1101001402731
Beschreibung:
N-WF ESD eyepiece, 15× (16 mm)
VE:
1 * 1 ST
Artikel-Nr:
(ILMV701321)
Lieferant:
Welch by Gardner Denver
Hersteller-Artikelnummer::
701321
Lokale Artikelnummer::
ILMV701321
Beschreibung:
Flanges with long tubulation, type KF, DN 16, Edelstahl
VE:
1 * 1 ST
Artikel-Nr:
(KRAF21754.5020)
Lieferant:
Bernd Kraft
Hersteller-Artikelnummer::
21754.5020
Lokale Artikelnummer::
KRAF21754.5020
Beschreibung:
Kaliumhydroxid 16% in wässriger Lösung, reinst
VE:
1 * 5 L
Artikel-Nr:
(BOSSBS-1472R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-1472R-FITC
Lokale Artikelnummer::
BOSSBS-1472R-FITC
Beschreibung:
Interferon (IFN) Inducible 16 (IFI16) protein belongs to a family of HIN 200 human and mouse proteins. IFI16 is a nuclear protein comtaining regulatory domains such as DNA binding domain, transcriptional regulatory domain and DAPIN/PAAD domain. IFI16 has three isotypes A, B, and C (85-95 kDa), which arise as a result of mRNA alternative splicing. All are phosphorylated on serine and threonine residues and can homo and heterodimerize. Expression is restricted to the nuclei of hematopoietic cells, fibroblasts and epithelial cells. IFI16 expression in hematopoietic cells of myeloid lineage is tightly regulated and highly induced in the differentiation and proliferation of the cell. Due to its localisation in the nucleus, regulation of protein expression, and ability to bind DNA, it is assumed that IFI16 has a role in transcription regulation of cell differentiation. In addition, it was found that IFI16 can act as a transcriptional repressor and is involved in regulation and activation of p53 in cancer cells.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9737R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9737R-A555
Lokale Artikelnummer::
BOSSBS-9737R-A555
Beschreibung:
The tetratricopeptide repeat (TPR) motif is a degenerate, 34 amino acid sequence found in many proteins and acts to mediate protein-protein interactions in various pathways. At the sequence level, there can be up to 16 tandem TPR repeats, each of which has a helix-turn-helix shape that stacks on other TPR repeats to achieve ligand binding specificity. EDRF1 (erythroid differentiation-related factor 1), also known as C10orf137 (chromosome 10 open reading frame 137), is a 1,238 amino acid protein containing two TPR repeats. Localizing to nucleus, EDRF1 is involved in transcriptional activation of globin genes by regulating DNA-binding activity of GATA-1 transcription factor. EDRF1 may also play an important role in organ development and histological differentiation. EDRF1 exists as four alternatively spliced isoforms and is encoded by a gene mapping to human chromosome 10q26.13.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11480R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11480R-A555
Lokale Artikelnummer::
BOSSBS-11480R-A555
Beschreibung:
Semaphorins are a family of cell surface and secreted proteins involved in neural development that are conserved from insects to humans. Members of this family are approximately 750 amino acids in length (including signal sequences) and are defined by a conserved extracellular “semaphorin†domain of approximately 500 amino acids containing 14-16 cysteines, blocks of conserved sequences and no obvious repeats. The transmembrane semaphorins are characterized by an additional 80 amino acid transmembrane domain and an 80-110 amino acid cytoplasmic domain. Secreted and cell-bound semaphorins chemically attract and repel the growth of neural axons, guiding the development of intricate networks of neural tissue. SEMA3E is a secreted semaphorin with 775 amino acids. Mutations in the SEMA3E gene are associated with CHARGE syndrome, a disorder characterized by cranial nerve dysfunction, coloboma of the eye, choanal atresia, inner and external ear abnormalities, cardiac anomalies, genitourinary abnormalities, and growth retardation.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11153R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11153R-A647
Lokale Artikelnummer::
BOSSBS-11153R-A647
Beschreibung:
Protocadherins are a large family of cadherin-like cell adhesion proteins that are involved in the establishment and maintenance of neuronal connections in the brain. There are three protocadherin gene clusters, designated alpha, beta and gamma, all of which contain multiple tandemly arranged genes. PCDHB12 (Protocadherin beta 12) is a 795 amino acid protein that is one of 16 proteins in the protocadherin beta cluster. Unlike the alpha and gamma gene clusters whose genes are spliced to downstream constant region exons during transcription, members of the beta cluster (such as PCDHB12) do not use constant-region exons to produce mRNAs. As a result, each protocadherin beta gene encodes the transmembrane, extracellular and short cytoplasmic domains of the protein. Localized to the cell membrane, PCDHB12 is a single-pass type I membrane protein that contains six cadherin domains. PCDHB12 may participate in the establishment and maintenance of specific neuronal connections in the brain.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11153R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11153R-A555
Lokale Artikelnummer::
BOSSBS-11153R-A555
Beschreibung:
Protocadherins are a large family of cadherin-like cell adhesion proteins that are involved in the establishment and maintenance of neuronal connections in the brain. There are three protocadherin gene clusters, designated alpha, beta and gamma, all of which contain multiple tandemly arranged genes. PCDHB12 (Protocadherin beta 12) is a 795 amino acid protein that is one of 16 proteins in the protocadherin beta cluster. Unlike the alpha and gamma gene clusters whose genes are spliced to downstream constant region exons during transcription, members of the beta cluster (such as PCDHB12) do not use constant-region exons to produce mRNAs. As a result, each protocadherin beta gene encodes the transmembrane, extracellular and short cytoplasmic domains of the protein. Localized to the cell membrane, PCDHB12 is a single-pass type I membrane protein that contains six cadherin domains. PCDHB12 may participate in the establishment and maintenance of specific neuronal connections in the brain.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11480R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11480R-A488
Lokale Artikelnummer::
BOSSBS-11480R-A488
Beschreibung:
Semaphorins are a family of cell surface and secreted proteins involved in neural development that are conserved from insects to humans. Members of this family are approximately 750 amino acids in length (including signal sequences) and are defined by a conserved extracellular “semaphorin†domain of approximately 500 amino acids containing 14-16 cysteines, blocks of conserved sequences and no obvious repeats. The transmembrane semaphorins are characterized by an additional 80 amino acid transmembrane domain and an 80-110 amino acid cytoplasmic domain. Secreted and cell-bound semaphorins chemically attract and repel the growth of neural axons, guiding the development of intricate networks of neural tissue. SEMA3E is a secreted semaphorin with 775 amino acids. Mutations in the SEMA3E gene are associated with CHARGE syndrome, a disorder characterized by cranial nerve dysfunction, coloboma of the eye, choanal atresia, inner and external ear abnormalities, cardiac anomalies, genitourinary abnormalities, and growth retardation.
VE:
1 * 100 µl
Lieferant:
Heidolph Instruments GmbH & Co.KG
Beschreibung:
Modell SP quick 1,6 und 2,5 mm.
Artikel-Nr:
(BOSSBS-15147R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15147R
Lokale Artikelnummer::
BOSSBS-15147R
Beschreibung:
C2orf16 (chromosome 2 open reading frame 16), also known as DKFZp434G118 or DKFZp781D2023, is a 1,984 amino acid protein encoded by a gene that maps to human chromosome 2p23.3. As the second largest human chromosome, chromosome 2 makes up approximately 8% of the human genome and contains 237 million bases encoding over 1,400 genes. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstré°‰ syndrome, is related to mutations in the ALMS1 gene. Chromosome 2 contains a probable vestigial second centromere as well as vestigial telomeres, which gives credence to the hypothesis that human chromosome 2 formed as a result of an ancient fusion of two ancestral chromosomes, which are still present in modern day apes.
VE:
1 * 100 µl
Lieferant:
IKA
Beschreibung:
Kreuzmuffe 6 - 16 mm Ø Stativ, 6 - 16 mm Ø Verlängerungsarm, Für: T 18 basic, T 25 digital
Artikel-Nr:
(QEDB57004)
Lieferant:
QED Bioscience
Hersteller-Artikelnummer::
57004
Lokale Artikelnummer::
QEDB57004
Beschreibung:
Anti-Amyloid Beta 1-16 Mouse Monoclonal Antibody
VE:
1 * 100 µG
Artikel-Nr:
(QEDB57003)
Lieferant:
QED Bioscience
Hersteller-Artikelnummer::
57003
Lokale Artikelnummer::
QEDB57003
Beschreibung:
Anti-Amyloid Beta 1-16 Mouse Monoclonal Antibody
VE:
1 * 100 µG
Preis auf Anfrage
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