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Isoprenoid Synthase Domain Containing (ISPD) ELISA Kits

ISPD encodes a 2-C-methyl-D-erythritol 4-phosphate cytidylyltransferase-like protein. Additionally we are shipping ISPD Antibodies (21) and ISPD Proteins (3) and many more products for this protein.

list all ELISA KIts Gene Name GeneID UniProt
ISPD 729920 A4D126
ISPD 75847 Q5RJG7
ISPD 493574 Q5S6T3
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Top ISPD ELISA Kits at antibodies-online.com

Showing 3 out of 3 products:

Catalog No. Reactivity Sensitivity Range Quantity Supplier Delivery Price Details
Rat
96 Tests Log in to see 11 to 13 Days
$875.60
Details
Mouse
96 Tests Log in to see 11 to 13 Days
$875.60
Details
Human
96 Tests Log in to see 11 to 13 Days
$875.60
Details

More ELISA Kits for ISPD Interaction Partners

Human Isoprenoid Synthase Domain Containing (ISPD) interaction partners

  1. ISPD gene homozygous deletion as a prenatal manifestation of Walker-Warburg syndrome has been found in 3 female fetuses of one family.

  2. Reduced levels of GYLTL1B (show GYLTL1B ELISA Kits) and ISPD mRNA associated with increased patient mortality and are the likely cause of alphaDG hypoglycosylation in ccRCC.

  3. study describes a new homozygous missense mutation c.367G>A (p.Gly123Arg) in the ISPD gene in a family of Pakistani origin with 2 cousins from consanguineous parents affected with a congenital muscular dystrophy (CMD (show ACAN ELISA Kits)) /early limb-girdle muscular dystrophy intermediate phenotype and CMD (show ACAN ELISA Kits) respectively

  4. study report the involvement of the ISPD gene in milder dystroglycanopathy phenotypes ranging from congenital muscular dystrophy to limb-girdle muscular dystrophy and identified allelic ISPD variants in nine cases belonging to seven families

  5. we identified a novel homozygous c.161G>C/p.G54A variant in ISPD in patients with limb-girdle muscular dystrophy

  6. TMEM5 mutations were frequently associated with gonadal dysgenesis and neural tube defects, and ISPD mutations were frequently associated with brain vascular anomalies.

  7. ISPD loss-of-function mutations disrupt dystroglycan (show DAG1 ELISA Kits) O-mannosylation and cause Walker-Warburg syndrome.

  8. Mutations in ISPD cause Walker-Warburg syndrome and defective glycosylation of alpha-dystroglycan.

Mouse (Murine) Isoprenoid Synthase Domain Containing (ISPD) interaction partners

  1. we show that activated NOTCH1 (show NOTCH1 ELISA Kits) and ZMIZ1 (show ZMIZ1 ELISA Kits) collaborate to induce T-ALL in mice

  2. This study demonistrated that the axonal guidance defects observed in ispd mutant mice.

ISPD Antigen Profile

Antigen Summary

This gene encodes a 2-C-methyl-D-erythritol 4-phosphate cytidylyltransferase-like protein. Mutations in this gene are the cause of Walker-Warburg syndrome. Alternate splicing results in multiple transcript variants.

Gene names and symbols associated with ISPD

  • isoprenoid synthase domain containing (ISPD) antibody
  • isoprenoid synthase domain containing (ispd) antibody
  • isoprenoid synthase domain containing (Ispd) antibody
  • 4930579E17Rik antibody
  • AV040780 antibody
  • MDDGA7 antibody
  • Nip antibody
  • sb:eu371 antibody
  • zgc:154151 antibody

Protein level used designations for ISPD

isoprenoid synthase domain containing , 2-C-methyl-D-erythritol 4-phosphate cytidylyltransferase-like protein , TGas037c08.1 , isoprenoid synthase domain-containing protein , 4-diphosphocytidyl-2C-methyl-D-erythritol synthase homolog , notch1-induced protein

GENE ID SPECIES
420591 Gallus gallus
548994 Xenopus (Silurana) tropicalis
714980 Macaca mulatta
744905 Pan troglodytes
100065851 Equus caballus
100391839 Callithrix jacchus
100436260 Pongo abelii
729920 Homo sapiens
75847 Mus musculus
493574 Rattus norvegicus
798716 Danio rerio
Selected quality suppliers for ISPD (ISPD) ELISA Kits
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