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2-Brom-4,5-dimethoxybenzoes\u00E4ure
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2-Brom-4,5-dimethoxybenzoes\u00E4ure
Lieferant:
Biotium
Beschreibung:
This MAb recognizes the 56.5 kDa (CK10); 50 kDa (CK14); 50 kDa (CK15); 48 kDa (CK16); 40 kDa (CK19) keratins of the acidic (Type I or LMW) subfamily. Twenty human keratins are resolved with two-dimensional gel electrophoresis into acidic (pI 6.0) subfamilies. The acidic keratins have molecular weights (MW) of 56.5, 55, 51, 50, 50', 48, 46, 45, and 40 kDa. MAb AE3 recognizes the 65-67, 64, 59, 58, 56, and 52 kDa keratins of basic subfamily. Many studies have shown the usefulness of keratins as markers in cancer research and tumor diagnosis. AE1/AE3 is a broad spectrum anti pan-keratin antibody cocktail, which differentiates epithelial tumors from non-epithelial tumors e.g. squamous vs. adenocarcinoma of the lung, liver carcinoma, breast cancer, and esophageal cancer.
Artikel-Nr:
(BOSSBS-10251R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-10251R-A488
Lokale Artikelnummer::
BOSSBS-10251R-A488
Beschreibung:
HLA-A belongs to the HLA class I heavy chain paralogues. This class I molecule is a heterodimer consisting of a heavy chain and a light chain (beta-2 microglobulin). The heavy chain is anchored in the membrane. Class I molecules play a central role in the immune system by presenting peptides derived from the endoplasmic reticulum lumen. They are expressed in nearly all cells. The heavy chain is approximately 45 kDa and its gene contains 8 exons. Exon 1 encodes the leader peptide, exons 2 and 3 encode the alpha1 and alpha2 domains, which both bind the peptide, exon 4 encodes the alpha3 domain, exon 5 encodes the transmembrane region, and exons 6 and 7 encode the cytoplasmic tail. Polymorphisms within exon 2 and exon 3 are responsible for the peptide binding specificity of each class one molecule. Typing for these polymorphisms is routinely done for bone marrow and kidney transplantation. Hundreds of HLA-A alleles have been described. [provided by RefSeq, Jul 2008]
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-12325R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12325R-A555
Lokale Artikelnummer::
BOSSBS-12325R-A555
Beschreibung:
PTCHD3 is a 767 amino acid multi-pass membrane protein that localizes to the midpiece of the sperm tail, where it is implicated in sperm function and development. A member of the patched family, PTCHD3 contains one SSD (sterol-sensing) domain and is encoded by a gene that maps to human chromosome 10p12.1. Spanning nearly 135 million base pairs, chromosome 10 makes up approximately 4.5% of total DNA in cells and encodes nearly 1,200 genes. Several protein-coding genes, including those that encode for chemokines, cadherins, excision repair proteins, early growth response factors (Egrs) and fibroblast growth receptors (FGFRs), are located on chromosome 10. Defects in some of the genes that map to chromosome 10 are associated with Charcot-Marie Tooth disease, Jackson-Weiss syndrome, Usher syndrome, nonsyndromatic deafness, Wolman’s syndrome, Cowden syndrome, multiple endocrine neoplasia type 2 and porphyria.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-12325R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12325R
Lokale Artikelnummer::
BOSSBS-12325R
Beschreibung:
PTCHD3 is a 767 amino acid multi-pass membrane protein that localizes to the midpiece of the sperm tail, where it is implicated in sperm function and development. A member of the patched family, PTCHD3 contains one SSD (sterol-sensing) domain and is encoded by a gene that maps to human chromosome 10p12.1. Spanning nearly 135 million base pairs, chromosome 10 makes up approximately 4.5% of total DNA in cells and encodes nearly 1,200 genes. Several protein-coding genes, including those that encode for chemokines, cadherins, excision repair proteins, early growth response factors (Egrs) and fibroblast growth receptors (FGFRs), are located on chromosome 10. Defects in some of the genes that map to chromosome 10 are associated with Charcot-Marie Tooth disease, Jackson-Weiss syndrome, Usher syndrome, nonsyndromatic deafness, Wolman’s syndrome, Cowden syndrome, multiple endocrine neoplasia type 2 and porphyria.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-12325R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12325R-A680
Lokale Artikelnummer::
BOSSBS-12325R-A680
Beschreibung:
PTCHD3 is a 767 amino acid multi-pass membrane protein that localizes to the midpiece of the sperm tail, where it is implicated in sperm function and development. A member of the patched family, PTCHD3 contains one SSD (sterol-sensing) domain and is encoded by a gene that maps to human chromosome 10p12.1. Spanning nearly 135 million base pairs, chromosome 10 makes up approximately 4.5% of total DNA in cells and encodes nearly 1200 genes. Several protein-coding genes, including those that encode for chemokines, cadherins, excision repair proteins, early growth response factors (Egrs) and fibroblast growth receptors (FGFRs), are located on chromosome 10. Defects in some of the genes that map to chromosome 10 are associated with Charcot-Marie Tooth disease, Jackson-Weiss syndrome, Usher syndrome, nonsyndromatic deafness, Wolman's syndrome, Cowden syndrome, multiple endocrine neoplasia type 2 and porphyria.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-12325R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12325R-A350
Lokale Artikelnummer::
BOSSBS-12325R-A350
Beschreibung:
PTCHD3 is a 767 amino acid multi-pass membrane protein that localizes to the midpiece of the sperm tail, where it is implicated in sperm function and development. A member of the patched family, PTCHD3 contains one SSD (sterol-sensing) domain and is encoded by a gene that maps to human chromosome 10p12.1. Spanning nearly 135 million base pairs, chromosome 10 makes up approximately 4.5% of total DNA in cells and encodes nearly 1,200 genes. Several protein-coding genes, including those that encode for chemokines, cadherins, excision repair proteins, early growth response factors (Egrs) and fibroblast growth receptors (FGFRs), are located on chromosome 10. Defects in some of the genes that map to chromosome 10 are associated with Charcot-Marie Tooth disease, Jackson-Weiss syndrome, Usher syndrome, nonsyndromatic deafness, Wolman’s syndrome, Cowden syndrome, multiple endocrine neoplasia type 2 and porphyria.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-12325R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12325R-A750
Lokale Artikelnummer::
BOSSBS-12325R-A750
Beschreibung:
PTCHD3 is a 767 amino acid multi-pass membrane protein that localizes to the midpiece of the sperm tail, where it is implicated in sperm function and development. A member of the patched family, PTCHD3 contains one SSD (sterol-sensing) domain and is encoded by a gene that maps to human chromosome 10p12.1. Spanning nearly 135 million base pairs, chromosome 10 makes up approximately 4.5% of total DNA in cells and encodes nearly 1200 genes. Several protein-coding genes, including those that encode for chemokines, cadherins, excision repair proteins, early growth response factors (Egrs) and fibroblast growth receptors (FGFRs), are located on chromosome 10. Defects in some of the genes that map to chromosome 10 are associated with Charcot-Marie Tooth disease, Jackson-Weiss syndrome, Usher syndrome, nonsyndromatic deafness, Wolman's syndrome, Cowden syndrome, multiple endocrine neoplasia type 2 and porphyria.
VE:
1 * 100 µl
Lieferant:
Alfa Aesar
Beschreibung:
Eosin B
Artikel-Nr:
(BOSSBS-8229R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8229R-CY7
Lokale Artikelnummer::
BOSSBS-8229R-CY7
Beschreibung:
Encoding over 1,100 genes within 132 million bases, chromosome 12 makes up about 4.5% of the human genome. A number of skeletal deformities are linked to chromosome 12 including hypochondrogenesis, achondrogenesis and Kniest dysplasia. Noonan syndrome, which includes heart and facial developmental defects among the primary symptoms, is caused by a mutant form of PTPN11 gene product, SH-PTP2. Chromosome 12 is also home to a homeobox gene cluster which encodes crucial transcription factors for morphogenesis, and the natural killer complex gene cluster encoding C-type lectin proteins which mediate the NK cell response to MHC I interaction. Trisomy 12p leads to facial development defects, seizure disorders and a host of other symptoms varying in severity depending on the extent of mosaicism and is most severe in cases of complete trisomy. The FAM101A gene product has been provisionally designated FAM101A pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(USBI132983)
Lieferant:
US Biological
Hersteller-Artikelnummer::
132983
Lokale Artikelnummer::
USBI132983
Beschreibung:
Anti-SAV1 Rabbit Polyclonal Antibody
VE:
1 * 100 µl
Artikel-Nr:
(POUL10.1444-45)
Lieferant:
Poulten & Graf
Hersteller-Artikelnummer::
10.1444-45
Lokale Artikelnummer::
POUL10.1444-45
Beschreibung:
Stopfen für Messkolben, PE-LD, mit Dichtungsprofil, NS: 45/40
VE:
1 * 10 ST
Artikel-Nr:
(231-2552)
Lieferant:
KOEHLER TECHNISCHE PRODUKTEN
Hersteller-Artikelnummer::
W-1407
Lokale Artikelnummer::
KOEHW-1407
Beschreibung:
Inoculating loop, Edelstahl, Impföse Ø: 4,5 mm, Grifflänge: 50 mm
VE:
1 * 1 ST
Artikel-Nr:
(EHERL20017700IO)
Lieferant:
EHRENSTORFER
Hersteller-Artikelnummer::
L20017700IO
Lokale Artikelnummer::
EHERL20017700IO
Beschreibung:
Organic Standard, 2,2',3,3',4,5',6'-Heptachlorbiphenyl (PCB Nr. 177) 10 µg/ml in Isooctan, Packung: Glasflasche
VE:
1 * 10 mL
Lieferant:
SOCOREX ISBA
Beschreibung:
Flaschenhalsadapter, mit Gewinde, PP, Außen-Ø 45 mm, für Modelle 520/525, Calibrex™
Artikel-Nr:
(CHMPFL13441.POR)
Lieferant:
CHEMPUR
Hersteller-Artikelnummer::
FL13441.POR
Lokale Artikelnummer::
CHMPFL13441.POR
Beschreibung:
6-Bromveratraldehyd
VE:
1 * 1 ST
Artikel-Nr:
(CHMPFL13461.POR)
Lieferant:
CHEMPUR
Hersteller-Artikelnummer::
FL13461.POR
Lokale Artikelnummer::
CHMPFL13461.POR
Beschreibung:
6-Bromveratraldehyd
VE:
1 * 1 ST
Preis auf Anfrage
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 noch angezeigt wird und Sie Hilfe benötigen, rufen Sie uns an 1-800-932 - 5000.
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noch angezeigt wird und Sie Hilfe benötigen, rufen Sie uns an 1-800-932 - 5000.
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