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BBS1 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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TJL T31 RH Data Chr 19 refs
Encodes Gene Bbs1, Bardet-Biedl syndrome 1 homolog (human), in MGI October 2003.
AW538199 matches at 3.0 e-127 to AF017128, Mus musculus fos-related antigen 1 (fra-1) gene, complete cds.
AW538437 matches at 3.2 e-128 to L26320, Mouse flap endonuclease-1 (FEN-1) mRNA, complete cds.
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TJL BSS Panel: Chr 19 refs
New nomen Bbs1, Bardet-Biedl syndrome 1 homolog (human) assigned April 2003.
mouse zona pellucida 1 gene, HindIII Southerns.
southern blot data for Tcell leukemia homeobox-1 (human Hox-11).
preproinsulin-1 gene mapped by PCR.
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BBS4 Recombinant Protein (P01)-Abnova Corporation
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author: Abnova
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ARF4L Recombinant Protein (Q01) Abnova-World Largest Monoclonal Antibody and Recombinant Protein Bank
Mutations in this gene have been associated with Bardet-Biedl syndrome (BBS).
Product Information - Product Description： ARF4L( AAH00043, 1 a.a.
-- -Applications ------ELISA, WB, Antibody Production, Assay Development, Protein Array Related Polyclonal Antibody -1 - match - H00000379-A01 ARF4L polyclonal antibody (A01...
author: Abnova
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Alstrom Syndrome Conference Report
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author: J rgen Naggert
subject: Alstrom Syndrome Conference Report
updated: 22/03/2006
matching:
bardet biedl syndrom 1
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Alstrom Syndrome Conference Report page 8
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author: J rgen Naggert
subject: Alstrom Syndrome Conference Report
updated: 22/03/2006
matching:
bardet biedl syndrom 1
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Medical Literature
Dyer DS, Wilson ME, Small KW, Pai GS (1994): Alstroem Syndrome: A case misdiagnosed as Bardet-Biedl Syndrome.
Whittington AV, Lambert SR, Dasher WB, Drack AV (1995): Electroretinography as a tool in distinguishing Bardet-Biedl and Alstroem syndromes in early childhood.- In: Lennerstrand G.- Update on Strabismus and Pediatric Ophthalmology:...
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Jurgen Naggert Staff Research Page - The Jackson Laboratory
Alstr?m syndrome and the phenotypically similar but genetically distinct Bardet-Biedl syndrome show a remarkable phenotypic similarity with the tubby mouse.
We hypothesize that tubby and Alstr?m syndrome (and Bardet-Biedl syndrome), which share many phenotypic features, function in the same pathway and have both early developmental...
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Patsy Nishina Staff Research Page - The Jackson Laboratory
The obesity, coupled with the retinal degeneration and hearing loss, makes tubby mice a good model for rare human monogenic disorders, particularly Bardet-Biedl and AlstrA¶m syndromes.
We are currently mapping and positionally cloning four new mouse obesity mutations.- AlstrA¶m Syndrome AlstrA¶m syndrome is a rare, recessive human...
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http://www.clontech.com/clontech/atlas/genelists/excel/huplastic12k.xls
...
article ID:
updated: 24/05/2005
matching:
bardet biedl syndrom 1
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PT3699-3E (PR27547) Hu Plas 12K
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author: emmachleder
updated: 22/08/2002
matching:
bardet biedl syndrom 1
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PT3699-3E (PR27547) Hu Plas 12K page 369
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author: emmachleder
updated: 22/08/2002
matching:
bardet biedl syndrom 1
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PT3699-3E (PR27547) Hu Plas 12K page 10
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author: emmachleder
updated: 22/08/2002
matching:
bardet biedl 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:
bardet biedl syndrom 1
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Microsoft Word - Document5
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author: Jan D. Marshall
updated: 22/03/2006
matching:
bardet biedl syndrom
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Retinal Degeneration 5 - The Jackson Laboratory
- Retinal Degeneration Genes Cataracts Other Mouse Models Screening FAQ Resources Picture Gallery About Dr.
The involvement of tub in obesity, retinal degeneration, and hearing loss suggests it as a model for the Alstrom (OMIM 203800) or Bardet-Biedl (OMIM 209900) syndromes.
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Alstrom Biography
It was at the Serafimerlasarettet Hospital in 1946 that he saw a 14 year old boy who appeared to have symptoms similar to the Laurence-Moon-Bardet-Biedl Syndrome, yet this patient's condition was different in several important ways.
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Nome
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author: francesca
updated: 21/03/2006
matching:
bardet biedl syndrom
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BBS7 polyclonal antibody (A01)-Abnova Corporation
Gene Information - Gene Name： BBS7 - Gene Ontology： GO:0007600 GO:0007601 - Gene Description： Bardet-Biedl syndrome 7 - Gene Alias： BBS2L1, FLJ10715 - - Entrez GeneID： 55212 - - GenBank Accession#： NM_018190 - - Omim ID： 209900|607590 - - Protein Accessio n# ： NP_060660 - Product Information -...
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BBS7 Recombinant Protein (Q01)-Abnova Corporation
Gene Information - Gene name： BBS7 - Gene Ontology： GO:0007600 GO:0007601 - Gene description： Bardet-Biedl syndrome 7 - - Gene alias： BBS2L1, FLJ10715 - - Entrez GeneID： 55212 - - GenBank Accession#： NM_018190 - - Omim ID： - - Protein Accession#： NP_060660 - - Product Information - Product...
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Nome page 4
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author: francesca
updated: 21/03/2006
matching:
bardet biedl
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Microsoft Word - Document12
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author: Jan D. Marshall
updated: 22/03/2006
matching:
bardet syndrom 1
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Alstrom Syndrome Conference Report page 10
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author: J rgen Naggert
subject: Alstrom Syndrome Conference Report
updated: 22/03/2006
matching:
biedl syndrom 1
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