anti-NIPA-Like Domain Containing 4 (NIPAL4) Antibodies

NIPAL4 likely encodes a membrane receptor. Additionally we are shipping NIPA-Like Domain Containing 4 Proteins (3) and many more products for this protein.

list all antibodies Gene Name GeneID UniProt
NIPAL4 348938 Q0D2K0
NIPAL4 214112 Q8BZF2
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Top anti-NIPA-Like Domain Containing 4 Antibodies at antibodies-online.com

Showing 10 out of 11 products:

Catalog No. Reactivity Host Conjugate Application Images Quantity Delivery Price Details
Human Rabbit Un-conjugated WB Host: Rabbit Target Name: NIPAL4 Sample Type: Hela Whole Cell lysates Antibody Dilution: 1.0ug/ml 100 μL 2 to 3 Days
$289.00
Details
Human Rabbit Un-conjugated WB 100 μL 11 to 14 Days
$551.83
Details
Human Rabbit Un-conjugated IHC (p) Immunohistochemical staining of human spleen with ICHTHYIN polyclonal antibody  shows strong cytoplasmic positivity in cells of red pulp. 100 μL 11 to 12 Days
$577.33
Details
Human Rabbit Biotin IHC, ELISA, WB   200 μL 11 to 14 Days
$1,101.83
Details
Human Rabbit Alkaline Phosphatase (AP) IHC, ELISA, WB   200 μL 11 to 14 Days
$1,101.83
Details
Human Rabbit FITC IHC, ELISA, WB   200 μL 11 to 14 Days
$1,101.83
Details
Human Rabbit HRP IHC, ELISA, WB   200 μL 11 to 14 Days
$1,101.83
Details
Human Rabbit PE IHC, ELISA, WB   200 μL 11 to 14 Days
$1,101.83
Details
Human Rabbit APC IHC, ELISA, WB   200 μL 11 to 14 Days
$1,101.83
Details
Human Rabbit Un-conjugated IHC, IHC (p), WB   400 μL 11 to 14 Days
$493.17
Details

More Antibodies against NIPA-Like Domain Containing 4 Interaction Partners

Human NIPA-Like Domain Containing 4 (NIPAL4) interaction partners

  1. NIPAL4 mutations are associated with Ichthyotic Phenotype.

  2. Case Report: novel NIPAL4 mutation in Japanese female with ichthyosiform erythroderma.

  3. We have identified a novel NIPAL4 mutation in two patients from Romania with autosomal recessive congenital ichthyosis.

  4. FATP4, ichthyin and TGM1 interact in lipid processing essential for maintaining the epidermal barrier function

  5. Autosomal recessive congenital ichthyosis patients with NIPAL4 mutations and abnormal ichthyin expression showed increased 12R-LOX and eLOX-3 staining and a colocalization signal of these lipoxygenases that was three times the normal intensity.

  6. combined findings indicate that ichthyin is associated with keratins and desmosomes in epidermis and is involved in lipid metabolism, possibly through processing of lamellar bodies

  7. diffuse yellowish keratoderma may be indicative of mutations in NIPAL4, providing an easily assessable genotype-phenotype correlation

  8. A recurrent missense mutation, p.A176D, was identified in individuals with autosomal recessive ichthyosis.

  9. Six homozygous mutations including one nonsense and five missense mutations were identified in a new gene, ichthyin, on chromosome 5q33 in patients with autosomal recessive congenital ichthyosis (ichthyin).

  10. mutations in ichthyin are associated with specific structural abnormalities in the granular layer of epidermis

  11. The results suggest that liarozole exerts a therapeutic effect in lamellar ichthyosis by mildly affecting the expression of retinoid- regulated genes in epidermis.

Mouse (Murine) NIPA-Like Domain Containing 4 (NIPAL4) interaction partners

  1. NIPAL4 is a putative Mg(2+) transporter, and Mg(2+) concentration in differentiated keratinocytes of Nipal4-KO mice was indeed lower than that of wild-type mice.

NIPA-Like Domain Containing 4 (NIPAL4) Antigen Profile

Protein Summary

This gene likely encodes a membrane receptor. Mutations in this gene have been associated with autosomal recessive congenital ichthyosis.

Gene names and symbols associated with NIPAL4

  • NIPA like domain containing 4 (NIPAL4) antibody
  • NIPA-like domain containing 4 (Nipal4) antibody
  • 9530066K23Rik antibody
  • ARCI6 antibody
  • ICHTHYIN antibody
  • ICHYN antibody

Protein level used designations for NIPAL4

NIPA-like protein 4 , magnesium transporter NIPA4 , non-imprinted in Prader-Willi/Angelman syndrome region protein 4 , ichthyin , non-imprinted in Prader-Willi/Angelman syndrome region protein 4 homolog

GENE ID SPECIES
348938 Homo sapiens
214112 Mus musculus
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