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3-Iodo-1H-indole-2-carbohydrazide
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3-Iodo-1H-indole-2-carbohydrazide
Artikel-Nr:
(BOSSBS-1163R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-1163R-A680
Lokale Artikelnummer::
BOSSBS-1163R-A680
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-1163R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-1163R-HRP
Lokale Artikelnummer::
BOSSBS-1163R-HRP
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:
(ABCRAB136367.0500)
Lieferant:
ABCR
Hersteller-Artikelnummer::
AB136367.0500
Lokale Artikelnummer::
ABCRAB136367.0500
Beschreibung:
6-Amino-1-naphthalinsulfonsäure ≥97,0% (durch HPLC, titrimetrische Analyse)
VE:
1 * 500 g
 This is a MarketSource item. Additional charges may apply
Artikel-Nr:
(BOSSBS-12502R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12502R-HRP
Lokale Artikelnummer::
BOSSBS-12502R-HRP
Beschreibung:
Apolipoproteins are a family of fatty-acid binding proteins that transport fat through the bloodstream in the form of lipoproteins. ApoO (Apolipoprotein O), also known as FAM121B or My025, is a 198 amino acid single-pass membrane protein that belongs to the apolipoprotein family. Expressed ubiquitously with particularly high expression in diabetic heart tissue, apoO functions to promote the transport of cholesterol from macrophage cells and may be involved in regulatory mechanisms that protect lipid accumulation within the heart. ApoO is present in high density lipoproteins (HDLs) and low density lipoproteins (LDLs) and is secreted by an MTP (microsomal triglyceride transfer protein)-dependent mechanism. Two isoforms of apoO exist due to alternative splicing events.
VE:
1 * 100 µl
Lieferant:
SIGMA ALDRICH MICROSCOPY
Beschreibung:
Hämatoxylin, Sigma-Aldrich®
Lieferant:
COMBI-BLOCKS
Beschreibung:
4-Amino-3-fluorbenzoesäure
Artikel-Nr:
(BOSSBS-4604R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-4604R-A488
Lokale Artikelnummer::
BOSSBS-4604R-A488
Beschreibung:
Leptin, the product of the ob (obese) gene, is a 16kD protein consisting of 146 amino acid residues. Leptin is produced in the adipose tissue, and is considered to play an important role in appetite control, fat metabolism and regulation of body weight. It targets the central nervous system, particularly hypothalamus, affecting food intake. Leptin levels are high in most obese individuals. Studies have shown that it may also influence reproductive function.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9355R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9355R-HRP
Lokale Artikelnummer::
BOSSBS-9355R-HRP
Beschreibung:
The gene encodes a 246-amino acid polypeptide containing an RNA binding motif, a putative nuclear localization signal, and phosphorylation sites. The alpha subunits comprises the outer rings of the proteasome. Some alpha subunits contain a functional nuclear localization signal; proteasomes are found in both the nuclear and cytoplasmic compartments of the cell. Alpha subunits may constitute a physical barrier that limits access of cytosolic proteins into the inner proteolytic chamber.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9355R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9355R-A647
Lokale Artikelnummer::
BOSSBS-9355R-A647
Beschreibung:
The gene encodes a 246-amino acid polypeptide containing an RNA binding motif, a putative nuclear localization signal, and phosphorylation sites. The alpha subunits comprises the outer rings of the proteasome. Some alpha subunits contain a functional nuclear localization signal; proteasomes are found in both the nuclear and cytoplasmic compartments of the cell. Alpha subunits may constitute a physical barrier that limits access of cytosolic proteins into the inner proteolytic chamber.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-4106R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-4106R-CY3
Lokale Artikelnummer::
BOSSBS-4106R-CY3
Beschreibung:
FANCG, involved in Fanconi anemia, confers resistance to both hygromycin and mitomycin C. FANCG contains a 5-prime GC-rich untranslated region characteristic of housekeeping genes. The putative 622-amino acid protein has a leucine-zipper motif at its N-terminus. Fanconi anemia is an autosomal recessive disorder with diverse clinical symptoms, including developmental anomalies, bone marrow failure, and early occurrence of malignancies. A minimum of 8 FA genes have been identified.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11683R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11683R-CY3
Lokale Artikelnummer::
BOSSBS-11683R-CY3
Beschreibung:
Thimet oligopeptidase, also designated soluble metallo-endopeptidase, is a cytoplasmic protein belonging to the peptidase M3 family. The gene for the protein maps against chromosome 19q13.3. Thimet oligopeptidase can degrade the b-Amyloid precursor protein and generate amyloidogenic fragments. It is important in cytoplasmic peptide degradation and involved in metabolism of neuropeptides that are less than 20 amino acids in length. Thimet oligopeptidase is highly expressed in testis but can also be detected in liver, lung and kidney.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-5353R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-5353R
Lokale Artikelnummer::
BOSSBS-5353R
Beschreibung:
FANCG, involved in Fanconi anemia, confers resistance to both hygromycin and mitomycin C. FANCG contains a 5-prime GC-rich untranslated region characteristic of housekeeping genes. The putative 622-amino acid protein has a leucine-zipper motif at its N-terminus. Fanconi anemia is an autosomal recessive disorder with diverse clinical symptoms, including developmental anomalies, bone marrow failure, and early occurrence of malignancies. A minimum of 8 FA genes have been identified.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-5353R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-5353R-CY3
Lokale Artikelnummer::
BOSSBS-5353R-CY3
Beschreibung:
FANCG, involved in Fanconi anemia, confers resistance to both hygromycin and mitomycin C. FANCG contains a 5-prime GC-rich untranslated region characteristic of housekeeping genes. The putative 622-amino acid protein has a leucine-zipper motif at its N-terminus. Fanconi anemia is an autosomal recessive disorder with diverse clinical symptoms, including developmental anomalies, bone marrow failure, and early occurrence of malignancies. A minimum of 8 FA genes have been identified.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8360R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8360R-A488
Lokale Artikelnummer::
BOSSBS-8360R-A488
Beschreibung:
The leucine-rich repeat-containing protein 2 (LRRC2) is a 371 amino acid protein that contains 9 LRR repeats. The gene encoding LRRC2 maps to chromosome 3, which encodes over 1,100 genes. Particular regions of the chromosome 3 short arm are deleted in many types of cancer cells. Marfan Syndrome, porphyria, von Hippel-Lindau syndrome, osteogenesis imperfecta and Charcot-Marie-Tooth Disease are a few of the numerous genetic diseases associated with chromosome 3.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11940R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11940R-A488
Lokale Artikelnummer::
BOSSBS-11940R-A488
Beschreibung:
Retinoic acid induced 1 (RAI1) is a 1,906 amino acid protein containing an N-terminal polyglutamine stretch that is expressed in most tissues, with highest expression in neuronal tissues. RAI1 functions as a transcriptional regulator and is important for embryonic and postnatal developments. Heterozygous deletions of the RAI1 gene are associated with Smith-Magenis syndrome (SMS), a mental retardation syndrome with behavioral, neurological and skeletal anomalies. Individuals affected with SMS usually display self-injurious behaviors, sleep disturbance, developmental delay and reduced motor and cognitive skills. RAI1 haploinsufficiency is specifically responsible for the obesity and craniofacial symptoms of SMS. RAI1 mutations have also been implicated in schizophrenia and spinocerebellar ataxia type 2.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9348R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9348R-CY5
Lokale Artikelnummer::
BOSSBS-9348R-CY5
Beschreibung:
ACLP2 (acid phosphatase-like 2), also known as UNQ370 or PRO706, is a 480 amino acid secreted protein that functions to catalyze the H2O-dependent conversion of a phosphate monoester to an alcohol and a phosphate. Expressed as two alternatively spliced isoforms, ACPL2 is encoded by a gene that maps to chromosome 3, which houses over 1,100 genes, including a chemokine receptor (CKR) gene cluster and a variety of human cancer-related gene loci. Key tumor suppressing genes on chromosome 3 include those that encode the apoptosis mediator RASSF1, the cell migration regulator HYAL1 and the angiogenesis suppressor SEMA3B. Marfan Syndrome, porphyria, von Hippel-Lindau syndrome, osteogenesis imperfecta and Charcot-Marie-Tooth Disease are a few of the numerous genetic diseases associated with chromosome 3.
VE:
1 * 100 µl
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 noch angezeigt wird und Sie Hilfe benötigen, rufen Sie uns an 1-800-932 - 5000.
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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