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Documents 1-22 out of 22 found
  Current Search:  zellweger: 22, syndrom: 3641, 1: 321133  

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PEX12 Recombinant Protein (P01)-Abnova Corporation
//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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PEX10 Recombinant Protein (P01)-Abnova Corporation
//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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PHYH Recombinant Protein (P01)-Abnova Corporation
Mutations in this gene have been associated with Refsum disease (RD) and deficient protein activity has been associated with Zellweger syndrome and rhizomelic chondrodysplasia punctata.
-- -Applications ------ELISA, WB, Antibody Production, Assay Development, Protein Array Related RNAi  -1 -  match - H00005264-R01 PHYH Pre-design Chimera RNAi -...
author: Abnova
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PEX6 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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IDI1 Recombinant Protein (Q01) Abnova-World Largest Monoclonal Antibody and Recombinant Protein Bank
It has been shown in peroxisomal deficiency diseases such as Zellweger syndrome and neonatal adrenoleukodystrophy that there is reduction in IPP isomerase activity.
-- -Applications ------ELISA, WB, Antibody Production, Assay Development, Protein Array Related Full-Length Recombinant Protein  -1 -  match - H00003422-P01 IDI1 Recombinant Protein (P01...
author: Abnova
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ACAA1 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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PXMP3 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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ABCD3 Recombinant Protein (P01) 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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SCP2 Recombinant Protein (P01) Abnova-World Largest Monoclonal Antibody and Recombinant Protein Bank
This gene is highly expressed in organs involved in lipid metabolism, and may play a role in Zellweger syndrome, in which cells are deficient in peroxisomes and have impaired bile acid synthesis.
-- -Applications ------ELISA, WB, Antibody Production, Assay Development, Protein Array Related Monoclonal Antibody  -1 -  match - H00006342-M01 SCP2...
author: Abnova
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PEX16 Recombinant Protein (P01) Abnova-World Largest Monoclonal Antibody and Recombinant Protein Bank
An inactivating nonsense mutation localized to this gene was observed in a patient with Zellweger syndrome of the complementation group CGD/CG9.
  Product Information - Product Description: PEX16( AAH00467, 1 a.a.

author: Abnova
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PXMP3 polyclonal antibody (A01)-Abnova Corporation
 Gene Information - Gene Name: PXMP3 - Gene Ontology: GO:0000151 GO:0004842 GO:0005777 GO:0005779 GO:0007031 GO:0008270 GO:0016021 GO:0016567 GO:0046872 - Gene Description: peroxisomal membrane protein 3, 35kDa (Zellweger syndrome) - Gene Alias: PAF-1, PAF1, PEX2, PMP35, RNF72 - - Entrez GeneID: 5828 - - GenBank Accession#&...
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http://www.clontech.com/clontech/atlas/genelists/excel/huToxII.xls
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article ID: updated: 24/05/2005 matching: zellweger syndrom 1
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PT3699-3E (PR27547) Hu Plas 12K page 58
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author: emmachleder updated: 22/08/2002 matching: zellweger syndrom 1
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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: zellweger syndrom 1
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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: zellweger syndrom 1
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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: zellweger syndrom 1
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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: zellweger syndrom 1
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Guinea-Pig Polyclonal Antiserum to DOUBLECORTIN (DCX)
Gleeson JG, Allen KM, Fox JW, Lamperti ED, Berkovic S, Scheffer I, Cooper EC, Dobyns WB, Minnerath SR, Ross ME, Walsh CA (1998) Doublecortin, a brain-specific gene mutated in human X-linked lissencephaly and double cortex syndrome, encodes a putative signaling protein.
(2000) A novel migration-related gene product, doublecortin, in neuronal migration disorder of fetuses and...
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Adrenoleukodystrophy Protein [ALDP] , a.a. 279-482 , clone 2AL-1D6 : MAB2164
MAB2164 can be used to analyze ALDP protein in cells and tissues from normal individuals, or from patients with adrenoleukodystrophy (ALD) or Zellweger syndrome and related peroxisomal diseases, and provides an excellent marker for peroxisomes (Mosser et al.
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Adrenoleukodystrophy Protein [ALDP] , a.a. 495-648 , clone 1AL-2B4 : MAB2162
MAB2162 can be used in Western blot, immunofluorescence or immunohistochemical studies to analyze the ALD protein in cells and tissues from normal individuals or from patients with adrenoleukodystrophy (ALD) or Zellweger syndrome and related peroxisomal diseases, and provides an excellent marker for peroxisomes(Mosser et al., 1994).
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Adrenoleukodystrophy Protein [ALDP] , a.a. 279-482 , clone 2AL-1D6 : MAB2164
MAB2164 can be used to analyze ALDP protein in cells and tissues from normal individuals, or from patients with adrenoleukodystrophy (ALD) or Zellweger syndrome and related peroxisomal diseases, and provides an excellent marker for peroxisomes (Mosser et al.
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Adrenoleukodystrophy Protein [ALDP] , a.a. 495-648 , clone 1AL-2B4 : MAB2162
MAB2162 can be used in Western blot, immunofluorescence or immunohistochemical studies to analyze the ALD protein in cells and tissues from normal individuals or from patients with adrenoleukodystrophy (ALD) or Zellweger syndrome and related peroxisomal diseases, and provides an excellent marker for peroxisomes(Mosser et al., 1994).
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