Huntingtin Associated Protein 1 (HAP1) Human shRNA Lentiviral Particle (Locus ID 9001)
CAT#: TL304153V
HAP1 - Human shRNA lentiviral particles (4 unique 29mer target-specific shRNA, 1 scramble control), 0.5 ml each, >10^7 TU/ml.
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CNY 11,400.00
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规格
Cited in 19 publications. |
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经常一起买 (3)
Specifications
Product Data | |
Product Name | Huntingtin Associated Protein 1 (HAP1) Human shRNA Lentiviral Particle (Locus ID 9001) |
Locus ID | 9001 |
Synonyms | HAP2; hHLP1; HIP5; HLP |
Vector | pGFP-C-shLenti |
Format | Lentiviral particles |
RefSeq | NM_001079870, NM_001079871, NM_003949, NM_177977, NM_177977.1, NM_177977.2, NM_001079870.1, NM_001079871.1, NM_003949.2, BC156728, NM_001367459, NM_001367460, NM_001367461, NM_001367462, NM_177977.3 |
Summary | Huntington's disease (HD), a neurodegenerative disorder characterized by loss of striatal neurons, is caused by an expansion of a polyglutamine tract in the HD protein huntingtin. This gene encodes a protein that interacts with huntingtin, with two cytoskeletal proteins (dynactin and pericentriolar autoantigen protein 1), and with a hepatocyte growth factor-regulated tyrosine kinase substrate. The interactions with cytoskeletal proteins and a kinase substrate suggest a role for this protein in vesicular trafficking or organelle transport. Several alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Jul 2008] |
shRNA Design | These shRNA constructs were designed against multiple splice variants at this gene locus. To be certain that your variant of interest is targeted, please contact techsupport@origene.com. If you need a special design or shRNA sequence, please utilize our custom shRNA service. |
Performance Guaranteed | OriGene guarantees that the sequences in the shRNA expression cassettes are verified to correspond to the target gene with 100% identity. One of the four constructs at minimum are guaranteed to produce 70% or more gene expression knock-down provided a minimum transfection efficiency of 80% is achieved. Western Blot data is recommended over qPCR to evaluate the silencing effect of the shRNA constructs 72 hrs post transfection. To properly assess knockdown, the gene expression level from the included scramble control vector must be used in comparison with the target-specific shRNA transfected samples. For non-conforming shRNA, requests for replacement product must be made within ninety (90) days from the date of delivery of the shRNA kit. To arrange for a free replacement with newly designed constructs, please contact Technical Services at techsupport@origene.com. Please provide your data indicating the transfection efficiency and measurement of gene expression knockdown compared to the scrambled shRNA control (Western Blot data preferred). |
Citations (19)
The use of this RNAi has been cited in the following citations: |
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The P5-type ATPase ATP13A1 modulates major histocompatibility complex I-related protein 1 (MR1)-mediated antigen presentation
,null,
The Journal of Biological Chemistry
,PubMed ID 34968463
[HAP1]
|
RanBP2/Nup358 enhances miRNA activity by sumoylating Argonautes
,null,
PLoS Genetics
,PubMed ID 33600493
[HAP1]
|
Quantitative genetic screening reveals a Ragulator-FLCN feedback loop that regulates the mTORC1 pathway.
,null,
Science signaling
,PubMed ID 32934076
[HAP1]
|
Transmembrane BAX Inhibitor-1 Motif Containing Protein 5 (TMBIM5) Sustains Mitochondrial Structure, Shape, and Function by Impacting the Mitochondrial Protein Synthesis Machinery
,null,
Cells
,PubMed ID 32977469
[HAP1]
|
NOXA upregulation by the prohibitin-binding compound fluorizoline is transcriptionally regulated by integrated stress response-induced ATF3 and ATF4.
,null,
The FEBS journal
,PubMed ID 32648994
[HAP1]
|
Recognition of Semaphorin Proteins by P. sordellii Lethal Toxin Reveals Principles of Receptor Specificity in Clostridial Toxins
,null,
Cell
,PubMed ID 32589945
[HAP1]
|
The TMEM189 gene encodes plasmanylethanolamine desaturase which introduces the characteristic vinyl ether double bond into plasmalogens
,null,
Proceedings of the National Academy of Sciences of the United States of America
,PubMed ID 32209662
[HAP1]
|
XPF-ERCC1 protects liver, kidney and blood homeostasis outside the canonical excision repair pathwaysXPF-ERCC1: Linchpin of DNA crosslink repair
,null,
PLoS Genetics
,PubMed ID 32271760
[HAP1]
|
MTHFD1 interaction with BRD4 links folate metabolism to transcriptional regulation
,null,
Nature genetics
,PubMed ID 31133746
[HAP1]
|
The transporters SLC35A1 and SLC30A1 play opposite roles in cell survival upon VSV virus infection
,null,
Scientific Reports
,PubMed ID 31320712
[HAP1]
|
Efficient and flexible tagging of endogenous genes by homology-independent intron targeting
,null,
Genome Research
,PubMed ID 31239279
[HAP1]
|
Huntingtin-Associated Protein 1A Regulates Store-Operated Calcium Entry in Medium Spiny Neurons From Transgenic YAC128 Mice, a Model of Huntington’s Disease
,null,
Frontiers in Cellular Neuroscience
,PubMed ID 30455632
[HAP1]
|
Accurate classification of BRCA1 variants with saturation genome editing
,null,
Nature
,PubMed ID 30209399
[HAP1]
|
KREMEN1 Is a Host Entry Receptor for a Major Group of Enteroviruses.
,null,
Cell host microbe
,PubMed ID 29681460
[HAP1]
|
Parallel reverse genetic screening in mutant human cells using transcriptomics
,null,
Molecular Systems Biology
,PubMed ID 27482057
[HAP1]
|
A generic strategy for CRISPR-Cas9-mediated gene tagging
,null,
Nature Communications
,PubMed ID 26674669
[HAP1]
|
Evidence that the endosomal sorting complex required for transport-II (ESCRT-II) is required for efficient human immunodeficiency virus-1 (HIV-1) production
,null,
Retrovirology
,PubMed ID 26268989
[HAP1]
|
Saturation Editing of Genomic Regions by Multiplex Homology-Directed Repair
,null,
Nature
,PubMed ID 25141179
[HAP1]
|
Megabase-scale deletion using CRISPR/Cas9 to generate a fully haploid human cell line
,null,
Genome Research
,PubMed ID 25373145
[HAP1]
|
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