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1-Butyl-5-chloro-1H-pyrazole
Lieferant:
EPPENDORF
Beschreibung:
Ersatz-Rotordeckel für Rotor F-45-32-5-PCR, Für: Rotor für Mikrozentrifugen, 5424
Artikel-Nr:
(BOSSBS-12325R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12325R-A488
Lokale Artikelnummer::
BOSSBS-12325R-A488
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-10251R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-10251R-A647
Lokale Artikelnummer::
BOSSBS-10251R-A647
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:
(PRSI27-586)
Lieferant:
ProSci Inc.
Hersteller-Artikelnummer::
27-586
Lokale Artikelnummer::
PRSI27-586
Beschreibung:
Lymphoid enhancer-binding factor-1 (LEF1) is a 48-kD nuclear protein that is expressed in pre-B and T cells. It binds to a functionally important site in the T-cell receptor-alpha enhancer and confers maximal enhancer activity. LEF1 belongs to a family of regulatory proteins that share homology with high mobility group protein-1.
VE:
1 * 100 µG
Artikel-Nr:
(BOSSBS-11002R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11002R
Lokale Artikelnummer::
BOSSBS-11002R
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 FAM62A gene product has been provisionally designated FAM62A pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8229R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8229R-CY5
Lokale Artikelnummer::
BOSSBS-8229R-CY5
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:
(BOSSBS-8229R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8229R
Lokale Artikelnummer::
BOSSBS-8229R
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:
(RIXI8-6020-45)
Lieferant:
RIXIUS
Hersteller-Artikelnummer::
8-6020-45
Lokale Artikelnummer::
RIXI8-6020-45
Beschreibung:
HDPE.
VE:
1 * 1 ST
Artikel-Nr:
(PROOMM0681.03)
Lieferant:
LGC Standards PROMOCHEM
Hersteller-Artikelnummer::
MM0681.03
Lokale Artikelnummer::
PROOMM0681.03
Beschreibung:
Organic Standard, 2,2'-Binaphthalene-6,6'-dicarboxylic acid
VE:
1 * 50 mg
Lieferant:
Shenandoah Biotechnology
Beschreibung:
Interleukin 22 (IL-22), also called IL-TIF, is an IL-10 family member that is produced by activated dendritic cells and T lymphocytes. IL-22 signals via a heteroduplex receptor consisting of IL-22R and IL-10RB chains. IL-22 is a potent mediator of cellular inflammatory responses and wound healing.
Lieferant:
Thermo Scientific
Beschreibung:
di-Kaliumoxalat Monohydrat 99+% zur Analyse
Lieferant:
Sampling Systems
Beschreibung:
Solid sampler, Sample insert, stainless steel, 2,2 ml
Artikel-Nr:
(CHMPFL13709.POR)
Lieferant:
CHEMPUR
Hersteller-Artikelnummer::
FL13709.POR
Lokale Artikelnummer::
CHMPFL13709.POR
Beschreibung:
Tetrabrom-p-benzochinon
VE:
1 * 1 ST
Artikel-Nr:
(BLEG409502)
Lieferant:
BIOLEGEND INC
Hersteller-Artikelnummer::
409502
Lokale Artikelnummer::
BLEG409502
Beschreibung:
Anti-Ig light chain κ Rat Monoclonal Antibody [clone: RMK-45]
VE:
1 * 500 µG
 This is a MarketSource item. Additional charges may apply
Lieferant:
Brand
Beschreibung:
Schraubkappen, Für: Laboratory bottles, Farbe: Blau, PP, Gewinde: GL 45
Artikel-Nr:
(USBI039994-BIOTIN)
Lieferant:
US Biological
Hersteller-Artikelnummer::
039994-BIOTIN
Lokale Artikelnummer::
USBI039994-BIOTIN
Beschreibung:
Anti-PI3KCB Rabbit Polyclonal Antibody (Biotin)
VE:
1 * 200 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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