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FGFR2 Recombinant Protein (P01)-Abnova Corporation
A full-length representative protein consists of an extracellular region, composed of three immunoglobulin-like domains, a single hydrophobic membrane-spanning segment and a cytoplasmic tyrosine kinase domain.
author: Abnova
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EYA1 Recombinant Protein (Q01) Abnova-World Largest Monoclonal Antibody and Recombinant Protein Bank
//ERROR MESSAGE RETURN====================================================================================== //var addmail="fyou@abnova.com.tw"; //window.onerror=function(errmsg,url,ln){ //if(window.confirm("A run-time error has occurred.\n\n Position:"+url+"\n line:"+ln+"\n This is an error message:"+errmsg+"\n\n Would you like to report to Abnova's webmaster?")){ //document...
author: Abnova
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DVL1 Recombinant Protein (Q01) Abnova-World Largest Monoclonal Antibody and Recombinant Protein Bank
//ERROR MESSAGE RETURN====================================================================================== //var addmail="fyou@abnova.com.tw"; //window.onerror=function(errmsg,url,ln){ //if(window.confirm("A run-time error has occurred.\n\n Position:"+url+"\n line:"+ln+"\n This is an error message:"+errmsg+"\n\n Would you like to report to Abnova's webmaster?")){ //document...
author: Abnova
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AR Recombinant Protein (Q01) Abnova-World Largest Monoclonal Antibody and Recombinant Protein Bank
//ERROR MESSAGE RETURN====================================================================================== //var addmail="fyou@abnova.com.tw"; //window.onerror=function(errmsg,url,ln){ //if(window.confirm("A run-time error has occurred.\n\n Position:"+url+"\n line:"+ln+"\n This is an error message:"+errmsg+"\n\n Would you like to report to Abnova's webmaster?")){ //document...
author: Abnova
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ROR2 Recombinant Protein (Q01) Abnova-World Largest Monoclonal Antibody and Recombinant Protein Bank
In addition, mutations in this gene can cause the autosomal recessive form of Robinow syndrome, which is characterized by skeletal dysplasia with generalized limb bone shortening, segmental defects of the spine, brachydactyly, and a dysmorphic facial appearance.
author: Abnova
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FGFR2 Recombinant Protein (Q01) Abnova-World Largest Monoclonal Antibody and Recombinant Protein Bank
A full-length representative protein consists of an extracellular region, composed of three immunoglobulin-like domains, a single hydrophobic membrane-spanning segment and a cytoplasmic tyrosine kinase domain.
author: Abnova
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FGFR3 Recombinant Protein (Q01) Abnova-World Largest Monoclonal Antibody and Recombinant Protein Bank
A full-length representative protein would consist of an extracellular region, composed of three immunoglobulin-like domains, a single hydrophobic membrane-spanning segment and a cytoplasmic tyrosine kinase domain.
author: Abnova
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FGFR1 Recombinant Protein (Q01) Abnova-World Largest Monoclonal Antibody and Recombinant Protein Bank
A full-length representative protein consists of an extracellular region, composed of three immunoglobulin-like domains, a single hydrophobic membrane-spanning segment and a cytoplasmic tyrosine kinase domain.
author: Abnova
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SGLT-1, Rat (Sodium Glucose Transporter 1)
-- Search - Molecular Biology Ion Channel Actin Actin Adipocytes Agarose Albumin All Other Amino Acids Angiopoietin Antibiotics Apoptosis Apoptosis A-I Aquaporin Assay Detection Assay Detection Binding Factors Binding Factors Biochemicals Cadherin Calcitonin Carbohydrates, Glycoproteins Cardiac Markers CD Markers CD Markers 101-150 CD Markers 51-75 Cells, Blood Components Centromeres...
duplicates:
http://www.usbio.net/Product.aspx?ProdSku=S1010-86C
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TGF-beta Ligands in Left-Right Development
In right isomerism, also called asplenia syndrome, the heart, lung and liver are double-right, and the spleen in absent.
The secreted C-terminal mature segment has 6 - 7 spatially conserved cysteines that form a cysteine knot structure in the monomer.
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The SLAM Family
1-3 In general, SLAM molecules possess two to four extracellular Ig domains, a transmembrane segment, and an intracellular tyrosine-rich region.
et al (2002) Immunogenetics 53:843.] The functional significance of SLAM family members is emphasized by their involvement in X-linked lymphoproliferative (XLP) disease, also known as Purtilo's syndrome and Duncan's...
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Promega Italia - Analisi delle Mutazioni
Unstable trinucleotide repeats have also been implicated in genetic diseases such as Fragile X Syndrome, Myotonic Dystrophy (MD), Huntington's Disease (HD) and Spinal Bulbar Atrophy (SBA).
Amplification of the gene segments by PCR (or, when investigating mRNA, by RT-PCR).
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Nucleic Acid Amplification Protocols and Applications Guide
Basic PCR The PCR process was originally developed to amplify short segments of a longer DNA molecule (Saiki et al.
(2003) Development of DNA vaccines against hemolytic-uremic syndrome in a murine model.A-Infect.
Use step cycles, not hold segments.
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Safe Water for Patient Care
Water temperatures at 30 - 40 °C in dead end pipe segments provide optimal growth conditions for some species of waterborne pathogens.
Transplant recipients, critically ill patients, neonates, and individuals with aquired immunodeficiency syndrome (AIDS) are most at risk of infection from environmental sources of microbial contamination.
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TJL T31 RH Data Chr X refs
Mouse chromosome 19 and distal rat chromosome 1: a chromosome segment conserved in evolution.
Mouse chromosome 19 and distal rat chromosome 1: a chromosome segment conserved in evolution.
DXErtd770e, DNA segment, Chr X, ERATO Doi 770, expressed.
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TJL T31 RH Data Chr 19 refs
AA407971 is DNA segment D19Mgi7 in MGI.
Mouse rod outer segment membrane protein 1 (Rom1) gene exons 1-3, complete cds.
MGI locus symbol: Rom1, rod outer segment membrane protein 1.
AA408137 is DNA segment D19Mgi1 in MGI.
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TJL T31 RH Data Chr 16 refs
MGI locus symbols included in this unannotated BAC: D16Jhu27, DNA segment, Chr 16, Johns Hopkins University 27; Hira, histone cell cycle regulation defective homolog A; Nlvcf, nuclear localization signal protein absent in velo-cardio-facial.
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TJL T31 RH Data Chr 15 refs
UniGene Cluster Mm.183022, D8Bwg1112e, DNA segment, Chr 8, Brigham & Women's Genetics 1112 expressed AA118123 - - - Reference: Avner P, Bruls T, Poras I, Eley L, Gas S, Ruiz P, Wiles MV, Sousa-Nunes R, Kettleborough R, Rana A, Morissette J, Bentley L, Goldsworthy M, Haynes A, Herbert E, Southam L, Lehrach H, Weissenbach J, Manenti G, Rodriguez-Tome P, Beddington R, Dunwoodie S,...
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TJL T31 RH Data Chr 11 refs
R75094 is DNA segment D11Mgi20 in MGI.
AA589469 is DNA segment D11Mgi24 in MGI.
AA409425 is DNA segment D11Mgi8 in MGI.
D83999 is DNA segment D11Mgi12 in MGI.
AA409132 is DNA segment D11Mgi21 in MGI.
AA673185 is DNA segment D11Mgi10 in MGI.
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TJL T31 RH Data Chr 8 refs
R75297 is DNA segment D8Mgi7 in MGI.
Encodes Gene Whsc1l1, Wolf-Hirschhorn syndrome candidate 1-like 1 homolog (human), in MGI October 2003.
AU022940 is DNA segment D14Mgi5 in MGI.
DNA segment, Chr 8, ERATO Doi 766, expressed.
AV207351 is DNA segment D8Mgi8 in MGI.
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TJL T31 RH Data Chr 5 refs
AU021133 is DNA segment D5Mgi8 in MGI.
AI851226 is DNA segment D5Mgi4 in MGI.
AI035639 is DNA segment D5Mgi2 in MGI.
Wfs1, Wolfram syndrome 1 homolog (human) in MGD.
MGI locus symbol: Wfs1, Wolfram syndrome 1 homolog.
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TJL T31 RH Data Chr 3 refs
R74830 is DNA segment D3Mgi5 in MGI.
AL024233 is DNA segment D3Mgi7 in MGI.
D3Ertd789e, DNA segment, Chr 3, ERATO Doi 789, expressed.
AW539211 is DNA segment D3Mgi6 in MGI.
AV071570 is DNA segment D3Mgi3 in MGI.
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TJL BSB Panel: Chr 13 refs
A heart segmental defect in the anterior/posterior axis of a transgenic mutant mouse.
A heart segmental defect in the anterior/posterior axis of a transgenic mutant mouse.
3.3 kb DNA segment flanking the transgene insertion in the htd mouse mutant, by PCR.
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TJL BSS Panel: Chr 13 refs
Defects in the cappuccino (cno) gene on mouse cgromosome 5 and human 4p cause Hermansky-Pudlak syndrome by an AP-3-independent mechanism.
A heart segmental defect in the anterior/posterior axis of a transgenic mutant mouse.
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TJL BSS Panel: Chr 7 refs
Defects in the cappuccino (cno) gene on mouse cgromosome 5 and human 4p cause Hermansky-Pudlak syndrome by an AP-3-independent mechanism.
PHR1 encodes an abundant, pleckstrin homology domain-containgin integral membrane protein in the photoreceptor outer segments.
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