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anti-IMP (Inosine 5'-Monophosphate) Dehydrogenase 1 (IMPDH1) Antibodies

The protein encoded by IMPDH1 acts as a homotetramer to regulate cell growth. Additionally we are shipping IMPDH1 Proteins (6) and many more products for this protein.

list all antibodies Gene Name GeneID UniProt
Anti-Rat IMPDH1 IMPDH1 362329  
IMPDH1 3614 P20839
Anti-Mouse IMPDH1 IMPDH1 23917 P50096
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Top anti-IMPDH1 Antibodies at antibodies-online.com

Showing 3 out of 3 products:

Catalog No. Reactivity Host Conjugate Application Images Quantity Supplier Delivery Price Details
Human Rabbit Un-conjugated EIA, IHC (p), WB Immunohistochemistry analysis in formalin fixed and paraffin embedded human breast tissue reacted with IMPDH1 / IMPD1 Antibody (N-term) followed by peroxidase conjugation of the secondary antibody and DAB staining. Western blot analysis of IMPDH1 / IMPD1 Antibody (N-term) in HL-60 cell line lysates (35ug/lane). This demonstrates the IMPDH1 antibody detected the IMPDH1 protein (arrow). 0.4 mL Log in to see 6 to 8 Days
$390.50
Details
Human Rabbit Un-conjugated WB WB Image Sample (30 ug of whole cell lysate) A: Raji 7.5% SDS PAGE antibody diluted at 1:1000 100 μL Log in to see 2 to 3 Days
$358.60
Details
Human Goat Un-conjugated EIA, IHC (p) Immunohistochemistry Image: Breast, Human: Formalin-Fixed, Paraffin-Embedded (FFPE) Immunohistochemistry Image: Placenta, Human: Formalin-Fixed, Paraffin-Embedded (FFPE) 50 μg Log in to see 6 to 8 Days
$500.50
Details

IMPDH1 Antibodies by Reactivity, Application, Clonality and Conjugate

Attributes Applications Host Clonality
Human ,
,

Top referenced anti-IMPDH1 Antibodies

  1. Human Polyclonal IMPDH1 Primary Antibody for EIA, IHC (p) - ABIN952892 : Ohmann, Burckart, Chen, Pravica, Brooks, Zeevi, Webber: Inosine 5'-monophosphate dehydrogenase 1 haplotypes and association with mycophenolate mofetil gastrointestinal intolerance in pediatric heart transplant patients. in Pediatric transplantation 2010 (PubMed)
    Show all 4 references for ABIN952892

More Antibodies against IMPDH1 Interaction Partners

Human IMP (Inosine 5'-Monophosphate) Dehydrogenase 1 (IMPDH1) interaction partners

  1. In our cohort of >300 familial cases of autosomal-recessive retinitis pigmentosa, PKRP004 is the only family harboring a mutation in IMPDH1.

  2. A novel mutation, p.L270R in IMPDH1, was found to be retinitis pigmentosa-causing in one family.

  3. p53 (show TP53 Antibodies) has a novel function in regulating purine biosynthesis, aided by miR (show MLXIP Antibodies)-34a-dependent IMPDH repression.

  4. IMPDH1 mutation is associated with retinitis pigmentosa.

  5. The mutation frequency of IMPDH1 gene of the Han population in Ganzhou city was similar as approximately 2-5% of the autosomal dominant retinitis pigmentosa cases among Americans of European origin and Europeans.

  6. resequenced IMPDH1 and IMPDH2 (show IMPDH2 Antibodies) using DNA from 288 individuals from three ethnic groups and performed functional genomic studies of the sequence variants observed; identified 73 single nucleotide polymorphisms in IMPDH1, 59 novel

  7. Inosine 5'-monophosphate dehydrogenase 1 haplotypes have a role in mycophenolate mofetil gastrointestinal intolerance in pediatric heart transplant patients

  8. The risk of subclinical acute rejection for recipients who cannot adapt in therapeutic drug monitoring of mycophenolic acid seems to be influenced by IMPDH1 rs2278293 polymorphism.

  9. In this small sample of pediatric heart transplant patients receiving MMF, ABCC2, IMPDH1 and IMPDH2 SNPs were associated with MMF GI intolerance and bone marrow toxicity.

  10. A novel IMPDH1 gene mutation (Arg231Pro) was associated with a severe form of autosomal dominant retinitis pigmentosa.

Cow (Bovine) IMP (Inosine 5'-Monophosphate) Dehydrogenase 1 (IMPDH1) interaction partners

  1. IMP (show BRAP Antibodies) dehydrogenase type 1 associates with polyribosomes translating rhodopsin (show RHO Antibodies) mRNA

Mouse (Murine) IMP (Inosine 5'-Monophosphate) Dehydrogenase 1 (IMPDH1) interaction partners

  1. We conclude that both IMPDH and HPRT (show HPRT1 Antibodies) activities contribute to normal T-lymphocyte activation and function

  2. Retinitis pigmentosa-causing mutations identified in IMPDH1 gene. High level of IMPDH1 in photoreceptors, low levels in other layers of retina.

  3. IMPDH1 mutations cause photoreceptor degeneration in retinitis pigmentosa

IMPDH1 Antigen Profile

Protein Summary

The protein encoded by this gene acts as a homotetramer to regulate cell growth. The encoded protein is an enzyme that catalyzes the synthesis of xanthine monophosphate (XMP) from inosine-5'-monophosphate (IMP). This is the rate-limiting step in the de novo synthesis of guanine nucleotides. Defects in this gene are a cause of retinitis pigmentosa type 10 (RP10). Several transcript variants encoding different isoforms have been found for this gene.

Gene names and symbols associated with IMPDH1

  • IMP (inosine 5'-monophosphate) dehydrogenase 1 (IMPDH1) antibody
  • IMP (inosine 5'-monophosphate) dehydrogenase 1 (impdh1) antibody
  • IMP (inosine 5'-monophosphate) dehydrogenase 1 (Impdh1) antibody
  • inosine 5'-phosphate dehydrogenase 1 (Impdh1) antibody
  • B930086D20Rik antibody
  • IMPD antibody
  • IMPD 1 antibody
  • IMPD1 antibody
  • IMPDH 1 antibody
  • LCA11 antibody
  • RP10 antibody
  • sWSS2608 antibody

Protein level used designations for IMPDH1

IMP (inosine 5'-monophosphate) dehydrogenase 1 , IMP (inosine monophosphate) dehydrogenase 1-like , IMP (inosine monophosphate) dehydrogenase 1 , inosine-5'-monophosphate dehydrogenase 1-like , IMP dehydrogenase 1 , inosine 5'-phosphate dehydrogenase 1 , inosine monophosphate dehydrogenase 1 , inosine-5'-monophosphate dehydrogenase 1 , IMPD 1 , IMPDH 1 , IMPDH-I

GENE ID SPECIES
100357217 Oryctolagus cuniculus
100399106 Callithrix jacchus
100442769 Pongo abelii
100480976 Ailuropoda melanoleuca
463864 Pan troglodytes
100552361 Anolis carolinensis
100583696 Nomascus leucogenys
362329 Rattus norvegicus
3614 Homo sapiens
504305 Bos taurus
23917 Mus musculus
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