anti-Retinoic Acid Induced 1 (RAI1) Antibodies

RAI1 is located within the Smith-Magenis syndrome region on chromosome 17. Additionally we are shipping Retinoic Acid Induced 1 Proteins (4) and and many more products for this protein.

list all antibodies Gene Name GeneID UniProt
RAI1 10743 Q7Z5J4
RAI1 19377 Q61818
RAI1 303188  
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Top anti-Retinoic Acid Induced 1 Antibodies at antibodies-online.com

Showing 10 out of 33 products:

Catalog No. Reactivity Host Conjugate Application Images Quantity Delivery Price Details
Human Rabbit Un-conjugated ELISA, WB   100 μg 11 to 14 Days
$419.83
Details
Human Mouse Un-conjugated ELISA, WB RAI1 monoclonal antibody (M01), clone 6H5. Western Blot analysis of RAI1 expression in Hela S3 NE. Detection limit for recombinant GST tagged RAI1 is 0.1 ng/ml as a capture antibody. 100 μg 11 to 12 Days
$440.00
Details
Human Rabbit Un-conjugated WB   200 μL 13 to 14 Days
$487.50
Details
Human Rabbit Un-conjugated ELISA   100 μg 11 to 14 Days
$419.83
Details
Human Rabbit Un-conjugated IF, IHC, IHC (p), IP, WB   100 μL 11 to 14 Days
$595.83
Details
Human Rabbit Biotin ELISA   100 μg 11 to 16 Days
$426.40
Details
Human Rabbit FITC ELISA   100 μg 11 to 16 Days
$426.40
Details
Human Rabbit HRP ELISA   100 μg 11 to 16 Days
$426.40
Details
Human Rabbit Un-conjugated ELISA, IF/ICC, IHC, WB   100 μg 11 to 16 Days
$426.40
Details
Human Rabbit Cy5 IF (p)   100 μL 14 to 21 Days
$416.90
Details

More Antibodies against Retinoic Acid Induced 1 Interaction Partners

Human Retinoic Acid Induced 1 (RAI1) interaction partners

  1. This study identified from multiethnic meta-analyses stronger associations between the RAI1 locus and non-REM apnea-hypopnea index in men compared with women.

  2. This study provides information about the inheritance pattern and recurrence risk for patients with identified variants and demonstrates clinical and genetic overlap of neurodevelopmental disorders

  3. we report molecular and clinical characterizations of six subjects with the reciprocal phenomenon of deletions spanning both genes, i.e., PMP22-RAI1 deletions. Systematic clinical studies revealed features consistent with SMS, including features of intellectual disability, speech and gross motor delays, behavioral problems and ocular abnormalities.

  4. RAI1 polymorphisms rs4925102 and rs9907986 are predicted to disrupt the binding of retinoic acid RXR-RAR receptors and the transcription factor DEAF1, respectively, in Smith-Magenis and Potocki-Lupski syndromes patients.

  5. Mutations in RAI1, OTOF, and SLC26A4 may have roles in nonsyndromic hearing loss in Altaian families in Siberia

  6. South American cohort did not confirm the effect of the four candidate loci as modifier of onset age: mithocondrial A10398G polymorphism and CAGn at RAI1, CACNA1A, ATXN3, and ATXN7 genes

  7. RAI1 Gene Duplication is associated with Potocki-Lupski syndrome.

  8. Results show that when MBD5 and RAI1 are haploinsufficient, they perturb several common pathways that are linked to neuronal and behavioral development.

  9. Human RAI1 protein was found to be a highly expressed neuronal protein whose distribution matches well with its role in cognitive and motor skills.

  10. RAI1 gene polyglutamine repeat has a different distribution in our population. The 14-repeat allele is associated with perinatal depression and more frequent experience of physical and psychological symptoms during menstrual period.

  11. evolutionary conservation of chromatin binding of SPBP and RAI1

  12. The Shc family protein adaptor, Rai, acts as a negative regulator of Th17 and Th1 cell development.

  13. A reduction of total RAI1 transcription factor activity is at the heart of the Smith-Magenis Syndrome clinical presentation.

  14. RAI1 is a positive transcriptional regulator of CLOCK, pinpointing a novel and important role for this gene in the circadian oscillator

  15. Mutation screening of the coding region of the RAI1 gene in patients with with features suggestive of Smith-Magenis syndrome identified two patients with novel heterozygous nonsynonymous alterations of unknown significance.

  16. Data suggest that RAI1 expression emerged as a genetic target for development of therapeutic interventions for SMS.

  17. Abnormal circadian rhythm of melatonin in Smith-Magenis syndrome patients with RAI1 point mutations

  18. Functional studies have shown that RAI1 gene dosage is crucial for normal regulation of circadian rhythm, lipid metabolism and neurotransmitter function.

  19. haploinsufficiency affects feeding, satiety and fat deposition patterns; RAI1 directly regulates the expression of BDNF

  20. data on 2 cases of Smith-Magenis syndrome with mutation of RAI1; sequencing of RAI1 revealed mutation of the same heptameric C-tract (CCCCCCC) in exon 3 in both cases (c.3103delC one case and and c.3103insC in the other), resulting in frameshift mutations

Mouse (Murine) Retinoic Acid Induced 1 (RAI1) interaction partners

  1. Haploinsufficiency of Retinoic Acid Induced 1 causes Smith-Magenis syndrome.

  2. Rai1 preferentially occupies DNA regions near active promoters and promotes the expression of a group of genes involved in circuit assembly and neuronal communication. Behavioral analyses demonstrated that pan-neural loss of Rai1 causes deficits in motor function, learning, and food intake.

  3. Mice haploinsufficient for Rai1 fed a high carbohydrate or a high fat diet gained weight at a significantly faster rate than their wild type littermates.

  4. Viral pseudo-enzymes activate RIG-I via deamidation to evade cytokine production.

  5. Rai1 dosage in forebrain neurons is critical during the development and is related to body weight regulation, activity levels and learning and memory.

  6. Rai1 is likely one of the main genes responsible for the circadian clock regulation

  7. The Shc family protein adaptor, Rai, acts as a negative regulator of Th17 and Th1 cell development.

  8. RAI1 is a positive transcriptional regulator of CLOCK, pinpointing a novel and important role for this gene in the circadian oscillator

  9. study provides evidence to show that Rai1 haploinsufficiency affects feeding, satiety and fat deposition patterns; RAI1 directly regulates the expression of BDNF

  10. transcriptional regulator, deficiency is responsible for obesity and craniofacial phenotypes in mice with SMS deletions

  11. Activation of the host response by RIG-I early in infection is important for controlling replication of West Nile virus NY

  12. Normal disomic Rai1 gene dosage was sufficient to rescue the complex physical and behavioral phenotypes observed in Dp(11)17/+ mice

  13. Genomic interval surrounding Rai1 are the major modifying genetic element(s) affecting the craniofacial penetrance

  14. Rai1 is a critical gene in the central nervous system functioning in a dosage sensitive manner and that the neurobehavioral phenotype is modified by regulator(s) in the approximately 590 kb genomic interval.

  15. Rai1 overexpression is associated with mental retardation, growth and developmental delays, and defective neurological and behavioral functions

  16. Distorted Mendelian transmission as a function of genetic background in Rai1-haploinsufficient mice is reported.

  17. Rai1 played an important role in the serotonin pathway in a dosage-dependent manner.

Retinoic Acid Induced 1 (RAI1) Antigen Profile

Protein Summary

This gene is located within the Smith-Magenis syndrome region on chromosome 17. It is highly similar to its mouse counterpart and is expressed at high levels mainly in neuronal tissues. The protein encoded by this gene includes a polymorphic polyglutamine tract in the N-terminal domain. Expression of the mouse counterpart in neurons is induced by retinoic acid. This gene is associated with both the severity of the phenotype and the response to medication in schizophrenic patients.

Gene names and symbols associated with RAI1

  • retinoic acid induced 1 (RAI1) antibody
  • retinoic acid induced 1 (Rai1) antibody
  • similar to S. cerevisiae RAI1 which enhances function of nuclear exonuclease Rat1 (RAI1) antibody
  • Gt1 antibody
  • RAI1 antibody
  • SMCR antibody
  • SMS antibody

Protein level used designations for RAI1

retinoic acid induced 1 , Smith-Magenis syndrome chromosome region , retinoic acid-induced protein 1 , hypothetical protein

GENE ID SPECIES
427664 Gallus gallus
489541 Canis lupus familiaris
528972 Bos taurus
699215 Macaca mulatta
743919 Pan troglodytes
10743 Homo sapiens
19377 Mus musculus
303188 Rattus norvegicus
3639576 Candida albicans SC5314
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