ascc1 gene Search Results


mouse ascc1 gene orf cdna clone expression plasmid, n-ofpspark tag  (Sino Biological)
N/A
Full length Clone DNA of Mouse activating signal cointegrator 1 complex subunit 1 with N terminal OFPSpark / RFP tag.
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rai1 mutation  (ROHHAD Fight Inc)
90
ROHHAD Fight Inc rai1 mutation
Schematic representation of chromosome 17, common 17p11.2 deletion, and <t>RAI1</t> . From left to right, the following are shown: the ideogram of G-band pattern of human chromosome 17; a schematic representation of the Smith–Magenis syndrome region with some representative genes; the RAI1 genomic and protein structure – glutamine-rich domain (Poly-Q), bipartite nuclear localization signals (NLS1 and NLS2), two serine-rich domains (Poly-S1 and Poly-S2), and C-terminal plant homeodomain (PHD); and the RAI1 mutations indexed in the HGMD™ Professional (version December 2015.4) known to date. * Indicates either frameshift or nonsense mutations.
Rai1 Mutation, supplied by ROHHAD Fight Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/ascc1+gene/ascc1+gene/pmc05680963-138-10-35
Average 90 stars, based on 1 article reviews
rai1 mutation - by Bioz Stars, 2026-10
90/100 stars
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mouse ascc1 gene orf cdna clone expression plasmid, c-his tag  (Sino Biological)
N/A
Full length Clone DNA of Mouse activating signal cointegrator 1 complex subunit 1 with C terminal His tag.
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rat ascc1 gene orf cdna clone in cloning vector  (Sino Biological)
N/A
Full length Clone DNA of Rat activating signal cointegrator 1 complex subunit 1.
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rat ascc1 gene lentiviral orf cdna expression plasmid, c-gfpspark tag  (Sino Biological)
N/A
Full length Clone DNA of Rattus norvegicus activating signal cointegrator 1 complex subunit 1.
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human ascc1 gene orf cdna clone expression plasmid, n-myc tag  (Sino Biological)
N/A
Full length Clone DNA of Human activating signal cointegrator 1 complex subunit 1 with N terminal Myc tag.
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mouse ascc1 gene orf cdna clone expression plasmid  (Sino Biological)
N/A
Full length Clone DNA of Mouse activating signal cointegrator 1 complex subunit 1.
   Buy from Supplier
human ascc1 gene orf cdna clone expression plasmid, c-ofpspark tag  (Sino Biological)
N/A
Full length Clone DNA of Human activating signal cointegrator 1 complex subunit 1 with C terminal OFPSpark / RFP tag.
   Buy from Supplier
mouse ascc1 gene orf cdna clone expression plasmid, c-ofpspark tag  (Sino Biological)
N/A
Full length Clone DNA of Mouse activating signal cointegrator 1 complex subunit 1 with C terminal OFPSpark / RFP tag.
   Buy from Supplier
mouse ascc1 gene orf cdna clone in cloning vector  (Sino Biological)
N/A
Full length Clone DNA of Mouse activating signal cointegrator 1 complex subunit 1.
   Buy from Supplier
mouse ascc1 gene orf cdna clone expression plasmid, n-ha tag  (Sino Biological)
N/A
Full length Clone DNA of Mouse activating signal cointegrator 1 complex subunit 1 with N terminal HA tag.
   Buy from Supplier
ascc1 mouse gene knockout kit  (OriGene)
N/A
Ascc1 KN2 0 Mouse gene knockout kit via CRISPR non homology mediated
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Image Search Results


Schematic representation of chromosome 17, common 17p11.2 deletion, and RAI1 . From left to right, the following are shown: the ideogram of G-band pattern of human chromosome 17; a schematic representation of the Smith–Magenis syndrome region with some representative genes; the RAI1 genomic and protein structure – glutamine-rich domain (Poly-Q), bipartite nuclear localization signals (NLS1 and NLS2), two serine-rich domains (Poly-S1 and Poly-S2), and C-terminal plant homeodomain (PHD); and the RAI1 mutations indexed in the HGMD™ Professional (version December 2015.4) known to date. * Indicates either frameshift or nonsense mutations.

Journal: The Application of Clinical Genetics

Article Title: RAI1 gene mutations: mechanisms of Smith–Magenis syndrome

doi: 10.2147/TACG.S128455

Figure Lengend Snippet: Schematic representation of chromosome 17, common 17p11.2 deletion, and RAI1 . From left to right, the following are shown: the ideogram of G-band pattern of human chromosome 17; a schematic representation of the Smith–Magenis syndrome region with some representative genes; the RAI1 genomic and protein structure – glutamine-rich domain (Poly-Q), bipartite nuclear localization signals (NLS1 and NLS2), two serine-rich domains (Poly-S1 and Poly-S2), and C-terminal plant homeodomain (PHD); and the RAI1 mutations indexed in the HGMD™ Professional (version December 2015.4) known to date. * Indicates either frameshift or nonsense mutations.

Article Snippet: – A recent study by Thaker et al identified a de novo RAI1 mutation in a child with morbid obesity and a clinical diagnosis of the Rapid-onset Obesity with Hypothalamic dysfunction, Hypoventilation and Autonomic Dysregulation (ROHHAD) syndrome.

Techniques: