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http://www.clontech.com/clontech/atlas/genelists/7931-1_HuPlastic12K.txt
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article ID:
updated: 22/08/2002
matching:
waardenburg syndrom type 2b
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http://www.clontech.com/clontech/atlas/genelists/7905-1_HuPlastic8K.txt
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article ID:
updated: 13/03/2002
matching:
waardenburg syndrom type 2b
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http://www.clontech.com/clontech/atlas/genelists/7903-1_7904-1_HuGlass38.txt
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article ID:
updated: 16/05/2001
matching:
waardenburg syndrom type 2b
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http://www.clontech.com/clontech/atlas/genelists/7900-1_HuGlass10.txt
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article ID:
updated: 16/05/2001
matching:
waardenburg syndrom type 2b
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PAX3 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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EDN3 Recombinant Protein (P01) Abnova-World Largest Monoclonal Antibody and Recombinant Protein Bank
The active peptide is a ligand for endothelin receptor type B (EDNRB).
Mutations in this gene and EDNRB have been associated with Hirschsprung disease (HSCR) and Waardenburg syndrome (WS), which are congenital disorders involving neural crest-derived cells.
author: Abnova
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Lab Vision Corporation
-ORDER PRODUCTS Order products with the click of a mouse!
The mutation of Mi causes Waardenburg Syndrome type II in humans.
Source:Recombinant human MiTF protein encoding aa 170-279 expressed in E.coli Characterization:On SDS-PAGE commassie blue stained gel, the purified recombinant protein shows a band at 39kDa including GST.
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Lab Vision Corporation
-ORDER PRODUCTS Order products with the click of a mouse!
The mutation of Mi causes Waardenburg Syndrome type II in humans.
In mice, a profound loss of pigmented cells in the skin eye and inner ear results, as well as osteopetrosis and defects in natural killer and mast cells.
Others not tested.
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Lab Vision Corporation
-ORDER PRODUCTS Order products with the click of a mouse!
The mutation of Mi causes Waardenburg Syndrome type II in humans.
Cellular Localization:Nuclear Please select from the items below to add to your shopping cart: Cat.
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Lab Vision Corporation
-ORDER PRODUCTS Order products with the click of a mouse!
The mutation of Mi causes Waardenburg Syndrome type II in humans.
Ab-2 reacts with both melanocytic and non-melanocytic isoforms of Mi.
# MS-772 - P0 - ( 0.1ml at 200ug/ml) ( Purified Ab with BSA and Azide) Cat.
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Lab Vision Corporation
-ORDER PRODUCTS Order products with the click of a mouse!
The mutation of Mi causes Waardenburg Syndrome type II in humans.
Comments: Ab-1 does not cross-react with other b-HLH-ZIP factors by DNA mobility shift assay.
Others not-known.
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Lab Vision Corporation
-ORDER PRODUCTS Order products with the click of a mouse!
The mutation of Mi causes Waardenburg Syndrome type II in humans.
Comments: Ab-3 cocktail is especially designed for sensitive detection of Mi protein.
Others not-known.
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master_table - The Jackson Laboratory
and Smith, R.J., Normal hearing in Splotch (Sp/+), the mouse homologue of Waardenburg syndrome type 1, Nat Genet, 2 (1992) 75-9.
and Read, A.P., Waardenburg syndrome type 2 caused by mutations in the human microphthalmia (MITF) gene [see comments], Nat Genet, 8 (1994) 251-5.
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Mouse Models - The Jackson Laboratory
(2005) Genomics 85: 582 MITF WS2A, Waardenburg syndrome, type IIA Tassabehji et al.
(1996) Development 122:3381 PAX3 WS1, Waardenburg syndrome type I WS3, Klein-Waardenburg syndrome Tassabehji et al.
(2001) Hum Mol Genet 10:153 SNAI2 - WS2, Waardenburg- syndrome, type-II- Sanchez-Martin et al.
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Microphthalmia (Mi), clone C5 : MAB3747
- - Search: - About This Product Product Datasheet References Information Library MSDS MAB3747 ----MAB3747 - MOUSE ANTI-MICROPHTHALMIA MONOCLONAL ANTIBODY CATALOG NUMBER: MAB3747 - LIST PRICE: Please click here to select your location, to view pricing - QUANTITY: 100 µg- - CLONE: C5 HOST/ISOTYPE: Ms IgG1 - - BACKGROUND: In Western blotting, it recognizes a doublet of 52-56kDa,...
duplicates:
http://www.chemicon.com/Product/ProductDataSheet.asp?ProductItem=MAB3747
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http://www.exalpha.com/pdfs/X1405M.pdf
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author: Scott
updated: 20/09/2005
matching:
waardenburg syndrom type
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http://www.exalpha.com/pdfs/X1405M.pdf page 1
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author: Scott
updated: 20/09/2005
matching:
waardenburg syndrom type
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PT3699-3E (PR27547) Hu Plas 12K page 82
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author: emmachleder
updated: 22/08/2002
matching:
waardenburg syndrom type
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NTD Bibliographical References from 1996 - The Jackson Laboratory
- Current NTD Strains Cryopreserved Strains Request Form NTD Bibliography NTD Home - 1996 UI - 96374819 : Asher JH Jr, Harrison RW, Morell R, Carey ML, Friedman TB.
Effects of Pax3 modifier genes on craniofacial morphology, pigmentation, and viability: a murine model of Waardenburg syndrome variation.
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NTD Bibliographical References from 1994 - The Jackson Laboratory
Waardenburg syndrome in man and splotch mutants in the mouse: a paradigm of the usefulness of linkage and synteny homologies in mouse and man for the genetic analysis of human congenital malformations.
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PAX3 polyclonal antibody (A01)-Abnova Corporation
Gene Information - Gene Name： PAX3 - Gene Ontology： GO:0003700 GO:0005634 GO:0006355 GO:0006366 GO:0006915 GO:0007275 GO:0007399 GO:0007605 - Gene Description： paired box gene 3 (Waardenburg syndrome 1) - Gene Alias： CDHS, HUP2, WS1 - - Entrez GeneID： 5077 - - GenBank Accession#： NM_000438 - - Omim ID： 122880|148820...
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http://www.clontech.com/clontech/atlas/genelists/7903-1_HuGlass38I.pdf page 112
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updated: 13/03/2002
matching:
waardenburg syndrom
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http://www.clontech.com/clontech/atlas/genelists/7905-1_HuPlastic8K.pdf page 62
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updated: 16/05/2001
matching:
waardenburg syndrom
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EBV Info
Six of the latent genes encode the nuclear antigens: EBNA-1 EBNA-2 EBNA-3A EBNA-3B EBNA-3C LP while three encode the latent membrane proteins: LMP-1 LMP-2A LMP-2B The most abundantly expressed latent transcripts in LCL are- non-polyadenylated RNA, the EBERs, which do not encode proteins, but are involved with avoidance of interferons.
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Proteins M-Z
Coli Equine Feline Firefly Frog Goat Goose Guinea Pig Hamster Human Insect Keyhole Limpet Hemocyanin Monkey Mouse Nematode Opossum Perch Photinus Pyralis Pigeon Porcine Rabbit Ram Rat Salmon Sheep Tetrahymena Xenopus Yeast Host Baboon Burro Canine Chicken Crab Shell Donkey Equine Goat Guinea Pig Hamster Horse Human Monkey Mouse R2997 Rabbit Rat Sheep Isotype IgG1 F(ab')2 F(c) Fab...
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