2\'-Amino-4\',5\'-dimethoxyacetophenon
Artikel-Nr:
(BOSSBS-1163R-CY5.5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-1163R-CY5.5
Lokale Artikelnummer::
BOSSBS-1163R-CY5.5
Beschreibung:
Defensins form a family of microbicidal and cytotoxic peptides made by neutrophils. Members of the defensin family are highly similar in protein sequence. This gene encodes defensin, beta 1, an antimicrobial peptide implicated in the resistance of epithelial surfaces to microbial colonization. This gene maps in close proximity to defensin family member, defensin, alpha 1 and has been implicated in the pathogenesis of cystic fibrosis. The mature form of Beta defensin 1 is 36 amino acids.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-15453R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15453R-FITC
Lokale Artikelnummer::
BOSSBS-15453R-FITC
Beschreibung:
HEMK2 is a 214 amino acid protein that belongs to the methyltransferase superfamily and exists as multiple alternatively spliced isoforms. The gene encoding HEMK2 maps to human chromosome 21, which houses approximately 300 genes and comprises nearly 1,5% of the human genome. Chromosome 21-associated disorders include Alzheimer's disease, amyotrophic lateral sclerosis and, most notably, Down syndrome (also known as trisomy 21).
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-12388R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12388R-CY5
Lokale Artikelnummer::
BOSSBS-12388R-CY5
Beschreibung:
KIF7 is a 1,343 amino acid protein expressed in embryonic stem cells, melanotic melanoma and Jurkat T-cells. KIF7 is a member of the KIF27 subfamily of the kinesin-like protein family and contains one kinesin-motor domain. It is suggested that KIF7 may participate in the Hedgehog (Hh) signaling pathway by regulating the proteolysis and stability of GLI transcription factors. Hedgehog (Hh) signaling plays a critical role in embryonic development.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-12340R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12340R
Lokale Artikelnummer::
BOSSBS-12340R
Beschreibung:
Vanin-2 is a 520 amino acid GPI-anchor protein that belongs to the CN hydrolase family and BTD/VNN subfamily.Widely expressed with high expression in spleen and blood, vanin-2 is suggested to be involved in thymus homing of bone marrow cells, regulation of Integrin ∫2-mediated cell adhesion, and migration and motility of neutrophils. Vanin-2 exists as five alternatively spliced isoforms and is encoded by a gene mapping to human chromosome 6q23.2.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-15453R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15453R-CY3
Lokale Artikelnummer::
BOSSBS-15453R-CY3
Beschreibung:
HEMK2 is a 214 amino acid protein that belongs to the methyltransferase superfamily and exists as multiple alternatively spliced isoforms. The gene encoding HEMK2 maps to human chromosome 21, which houses approximately 300 genes and comprises nearly 1,5% of the human genome. Chromosome 21-associated disorders include Alzheimer's disease, amyotrophic lateral sclerosis and, most notably, Down syndrome (also known as trisomy 21).
VE:
1 * 100 µl
Lieferant:
COMBI-BLOCKS
Beschreibung:
2-Amino-6-methylbenzothiazol
Artikel-Nr:
(BOSSBS-15078R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15078R-A680
Lokale Artikelnummer::
BOSSBS-15078R-A680
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:
(CHMPFL19487.POR)
Lieferant:
CHEMPUR
Hersteller-Artikelnummer::
FL19487.POR
Lokale Artikelnummer::
CHMPFL19487.POR
Beschreibung:
4-Amino-2-chlorpyridin
VE:
1 * 1 ST
Artikel-Nr:
(ENAMEN30009840.1G)
Lieferant:
SIA ENAMINE
Hersteller-Artikelnummer::
EN30009840.1G
Lokale Artikelnummer::
ENAMEN30009840.1G
Beschreibung:
2-Amino-N-propylbenzamid
VE:
1 * 1 g
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Artikel-Nr:
(ENAMEN30009734.1G)
Lieferant:
SIA ENAMINE
Hersteller-Artikelnummer::
EN30009734.1G
Lokale Artikelnummer::
ENAMEN30009734.1G
Beschreibung:
2-Amino-N-cyclopropylbenzamid
VE:
1 * 1 g
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Artikel-Nr:
(BOSSBS-5467R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-5467R
Lokale Artikelnummer::
BOSSBS-5467R
Beschreibung:
Gamma Catenin is a common junctional plaque protein. The membrane-associated plaques are architectural elements in an important strategic position to influence the arrangement and function of both the cytoskeleton and the cells within the tissue. The presence of gamma Catenin in both the desmosomes and in the intermediate junctions suggests that it plays a central role in the structure and function of submembranous plaques. It is a member of the catenin family since it contains a distinct repeating amino acid motif called the armadillo repeat.
VE:
1 * 100 µl
Artikel-Nr:
(ABCAAB154055-100)
Lieferant:
Abcam
Hersteller-Artikelnummer::
AB154055-100
Lokale Artikelnummer::
ABCAAB154055-100
Beschreibung:
Anti-Phosphoserine Aminotransferase Rabbit Polyclonal Antibody
VE:
1 * 100 µl
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Lieferant:
FLUOROCHEM
Beschreibung:
2-Amino-4-methylthiazol
Lieferant:
COMBI-BLOCKS
Beschreibung:
2-Amino-5-brompyridin
Artikel-Nr:
(MOLEM20340532)
Lieferant:
Molekula
Hersteller-Artikelnummer::
M20340532
Lokale Artikelnummer::
MOLEM20340532
Beschreibung:
2-Amino-5-brompyrimidin
VE:
1 * 5 g
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Artikel-Nr:
(BOSSBS-5855R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-5855R
Lokale Artikelnummer::
BOSSBS-5855R
Beschreibung:
ADAM32 was first discovered in a search for testis-specific proteinases. ADAM32 was identified in human, rat, mouse, macaque and chimp, and thus far has been found only in testis. In mice, ADAM32 is found on the sperm surface, where it may play a role in fertilization. ADAM32 is a member of the ADAMs family (A Disintegrin And Metalloproteinase), but does not contain the canonical HExxHxxxxH zinc-binding metalloproteinase catalytic site. The domain structure of the full length ADAM32 includes a signal sequence, propeptide domain, metalloproteinase-like domain, disintegrin-like domain, cys-rich domain, EGF-like domain, a short spacer region, then the transmembrane domain and a cytoplasmic domain. Like many of the reproductive-specific ADAMS, ADAM32 plays a non-enzymatic role, or (as is the case for ADAMs 1 & 2 (fertilin alpha and beta)), the protein acts in concert with a proteolytically active ADAM to process proteins. Little is known about interactions between ADAM32 and other ADAMs. Several different sequences for human ADAM32 are published; 787, 688, 649, 629, and 279 amino acids in length. The 688 amino acid form is identical to the 787 AA form until the EGF-like domain, and lacks the TM and cytoplasmic domains. The 649 AA form is likewise identical to the longer form, just to the start of the TM domain, and also lacks the TM and cytoplasmic domains. The 629 AA form has a deletion of 107 residues midway into the MP-like domain, and lacks the amino end of the disintegrin domain, but contains the rest of the domains found in the full-length ADAM32. The predicted masses for the different versions are 87.8, 76.9, 72.9, 70.9 and 32.1, respectively, for the 786, 688, 649, 629 and 279 AA forms.
VE:
1 * 100 µl
Preis auf Anfrage
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