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(\\\\\\\\u00B1)11(12)-EET+methyl+ester
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(\\\\\\\\u00B1)11(12)-EET+methyl+ester
Lieferant:
Alfa Aesar
Beschreibung:
Benzolsulfonsäure ≥94%
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
N-(tert-Butoxycarbonyl)-1,4-diaminobutan 97%
Artikel-Nr:
(BOSSBS-12479R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12479R-A750
Lokale Artikelnummer::
BOSSBS-12479R-A750
Beschreibung:
TMEM16C is a 981 amino acid multi-pass membrane protein that is encoded by a gene which maps to chromosome 11. With approximately 135 million base pairs and 1400 genes, chromosome 11 makes up around 4% of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. The blood disorders Sickle cell anemia and thalassemia are caused by HBB gene mutations, while Wilms' tumours, 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-12068R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12068R-A680
Lokale Artikelnummer::
BOSSBS-12068R-A680
Beschreibung:
TMEM132A is a 560 amino acid protein encoded by a gene mapping to human chromosome 11. With approximately 135 million base pairs and 1400 genes, chromosome 11 makes up around 4% of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. The blood disorders Sickle cell anemia and thalassemia are caused by HBB gene mutations. Wilms' tumours, 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-9935R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9935R-A680
Lokale Artikelnummer::
BOSSBS-9935R-A680
Beschreibung:
C11orf16 is a 404 amino acid protein that is encoded by a gene located on human chromosome 11. With approximately 135 million base pairs and 1400 genes, chromosome 11 makes up around 4% of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. The blood disorders Sickle cell anemia and _ thalassemia are caused by HBB gene mutations. Wilms' tumours, 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-12068R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12068R-FITC
Lokale Artikelnummer::
BOSSBS-12068R-FITC
Beschreibung:
TMEM132A is a 560 amino acid protein encoded by a gene mapping to human chromosome 11. 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. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. The blood disorders Sickle cell anemia and ∫ thalassemia are caused by HBB gene mutations. 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-12068R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12068R-A488
Lokale Artikelnummer::
BOSSBS-12068R-A488
Beschreibung:
TMEM132A is a 560 amino acid protein encoded by a gene mapping to human chromosome 11. 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. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. The blood disorders Sickle cell anemia and ∫ thalassemia are caused by HBB gene mutations. 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
Lieferant:
ANSELL HEALTH CARE
Beschreibung:
Fingerfertigkeit mit hervorragendem Schnittschutz für optimale Produktivität.
Lieferant:
Alfa Aesar
Beschreibung:
4-Biphenylmethanol ≥98%
Artikel-Nr:
(BOSSBS-9102R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9102R-A488
Lokale Artikelnummer::
BOSSBS-9102R-A488
Beschreibung:
Belongs to the sulfatase family. Sulfatases such as ARSK, hydrolyze sulfate esters from sulfated steroids,carbohydrates, proteoglycans, and glycolipids. They are involved in hormone biosynthesis, modulation of cell signaling, and degradation of macromolecules.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9102R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9102R-FITC
Lokale Artikelnummer::
BOSSBS-9102R-FITC
Beschreibung:
Belongs to the sulfatase family. Sulfatases such as ARSK, hydrolyze sulfate esters from sulfated steroids,carbohydrates, proteoglycans, and glycolipids. They are involved in hormone biosynthesis, modulation of cell signaling, and degradation of macromolecules.
VE:
1 * 100 µl
Artikel-Nr:
(APOSOR322800-100MG)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR322800-100MG
Lokale Artikelnummer::
APOSOR322800-100MG
Beschreibung:
SBAP (Succinimidyl 3-(bromoacetamido)propionate)
VE:
1 * 100 mg
Artikel-Nr:
(BOSSBS-7091R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-7091R
Lokale Artikelnummer::
BOSSBS-7091R
Beschreibung:
TP53I11 (Tumor protein p53 inducible protein 11), also referred to as PIG11 (p53-induced gene 11), is an early transcriptional target of tumor suppressor p53. It is up-regulated in the induction of apoptosis or cell growth inhibition by multiple chemopreventive agents. However, its biological role remains unclear.
VE:
1 * 100 µl
Lieferant:
Alfa Aesar
Beschreibung:
Acroleindiethylacetal 96%
Artikel-Nr:
(BOSSBS-9101R-CY5.5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9101R-CY5.5
Lokale Artikelnummer::
BOSSBS-9101R-CY5.5
Beschreibung:
Sulfatases hydrolyze sulfate esters from sulfated steroids, carbohydrates, proteoglycans and glycolipids. They are involved in hormone biosynthesis, modulation of cell signaling and degradation of macromolecules. Arylsulfatase H, also known as ARSH, is a 562 amino acid protein that belongs to the sulfatase family of bone and cartilage matrix proteins. Localized to the plasma membrane, Arylsulfatase H uses calcium as a cofactor to hydrolyze sulfate esters. The gene encoding Arylsulfatase D maps to human chromosome X, which contains nearly 153 million base pairs and houses over 1,000 genes. In conjunction with chromosome Y, chromosome X is responsible for sex determination. There are a number of conditions related to an abnormal number and combination of sex chromosomes, some of which include Turner's syndrome, color blindness, hemophilia and Duchenne muscular dystrophy.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-2305R-CY5.5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-2305R-CY5.5
Lokale Artikelnummer::
BOSSBS-2305R-CY5.5
Beschreibung:
E2 EPF is a member of the ubiquitin conjugating enzyme family. It is able to form a thiol ester linkage with ubiquitin in a ubiquitin activating enzyme dependent manner, a characteristic property of ubiquitin carrier proteins.
VE:
1 * 100 µl
Preis auf Anfrage
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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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