Solute Carrier Family 9, Subfamily A (NHE9, Cation Proton Antiporter 9), Member 9 Protéines (SLC9A9)

SLC9A9 encodes a sodium/proton exchanger that is a member of the solute carrier 9 protein family. De plus, nous expédions Solute Carrier Family 9, Subfamily A (NHE9, Cation Proton Antiporter 9), Member 9 Anticorps (70) et et beaucoup plus de produits pour cette protéine.

afficher tous les protéines Gène GeneID UniProt
SLC9A9 285195 Q8IVB4
SLC9A9 331004 Q8BZ00
Rat SLC9A9 SLC9A9 363115  
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Catalogue No. Origin Source Conjugué Images Quantité Fournisseur Livraison Prix Détails
Cellules d'insectes Humain rho-1D4 tag „Crystallography Grade“ protein due to multi-step, protein-specific purification process 0.5 mg Connectez-vous pour afficher 50 to 55 Days
$7,626.01
Détails
Cellules d'insectes Souris rho-1D4 tag „Crystallography Grade“ protein due to multi-step, protein-specific purification process 0.25 mg Connectez-vous pour afficher 50 to 55 Days
$5,355.45
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Wheat germ Humain GST tag 10 μg Connectez-vous pour afficher 11 to 12 Days
$414.29
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SLC9A9 Protéines protéines par origine et source

Origin Exprimée danse Conjugué
Human ,
,
Mouse (Murine)

Plus protéines pour Solute Carrier Family 9, Subfamily A (NHE9, Cation Proton Antiporter 9), Member 9 (SLC9A9) partenaires d'interaction

Human Solute Carrier Family 9, Subfamily A (NHE9, Cation Proton Antiporter 9), Member 9 (SLC9A9) interaction partners

  1. downregulation of miR (Montrer MLXIP Protéines)-135a as a potential mechanism underlying the high NHE9 expression observed in subset of glioblastomas

  2. SLC9A9 is a sodium hydrogen exchanger (Montrer SLC9A3R2 Protéines) present in the recycling endosome and highly expressed in the brain.

  3. SLC9A9 has an oncogenic function by being related to EGFR (Montrer EGFR Protéines) signaling, suggesting SLC9A9 may be a novel prognostic indicator and a therapeutic target in colorectal cancer

  4. Ectopic expression of NHE9 in human brain microvascular endothelial cells without external cues induced up-regulation of the transferrin receptor (TfR) and down-regulation of ferritin (Montrer FTL Protéines), leading to an increase in iron uptake

  5. Taken together, our findings demonstrate that NHE9 can be an effective predictor of chemoradiotherapy response in esophageal squamous cell carcinoma

  6. the expression of SLC9A9 can be a prognostic predictor for ESCC.

  7. SLC9A9 appears to influence the differentiation of T cells to a proinflammatory fate and may have a broader role in multiple sclerosis disease activity. There is an association between rs9828519(G) and nonresponse to IFNbeta treatment.

  8. find interesting gene expression changes in endosomal NHE6 (Montrer SLC9A6 Protéines) and NHE9 in postmortem autism brains.

  9. Loss-of-function mutations in NHE9 may contribute to autistic phenotype by modulating synaptic membrane protein expression and neurotransmitter clearance.

  10. 33 directly measured and 13 derived glycosylation traits in 3533 individuals were identified and three novel gene association (MGAT5 (Montrer MGAT5 Protéines), B3GAT1 (Montrer B3GAT1 Protéines) and SLC9A9) were identified using an additional European cohort.

Mouse (Murine) Solute Carrier Family 9, Subfamily A (NHE9, Cation Proton Antiporter 9), Member 9 (SLC9A9) interaction partners

  1. Inactivation of NHE9 in mice reproduces behavioral features of autism spectrum disorders including impaired social interaction, repetitive behaviors, and altered sensory processing.

  2. This is the first animal behavior study that links Slc9a9 to Autism spectrum disorders.

  3. Loss-of-function mutations in NHE9 may contribute to autistic phenotype by modulating synaptic membrane protein expression and neurotransmitter clearance.

  4. NHE9/Slc9a9 is expressed in the inner ear

Profil protéine Solute Carrier Family 9, Subfamily A (NHE9, Cation Proton Antiporter 9), Member 9 (SLC9A9)

Profil protéine

This gene encodes a sodium/proton exchanger that is a member of the solute carrier 9 protein family. The encoded protein localizes the to the late recycling endosomes and may play an important role in maintaining cation homeostasis. Mutations in this gene are associated with autism susceptibility 16 and attention-deficit/hyperactivity disorder.

Gene names and symbols associated with SLC9A9

  • solute carrier family 9 member A9 (SLC9A9)
  • solute carrier family 9 (sodium/hydrogen exchanger), member 9 (Slc9a9)
  • solute carrier family 9 member A9 (Slc9a9)
  • solute carrier family 9, subfamily A (NHE9, cation proton antiporter 9), member 9 (slc9a9)
  • 5730527A11Rik Protéine
  • 9930105B05 Protéine
  • AI854429 Protéine
  • AUTS16 Protéine
  • Nhe9 Protéine
  • RGD1560736 Protéine
  • SLC9A9 Protéine

Protein level used designations for SLC9A9

Na(+)/H(+) exchanger 9 , putative protein product of Nbla00118 , sodium/hydrogen exchanger 9 , sodium/proton exchanger NHE9 , solute carrier family 9 (sodium/hydrogen exchanger) , solute carrier family 9 member 9 , solute carrier family 9 (sodium/hydrogen exchanger), member 9 , sodium/hydrogen exchanger 9-like

GENE ID SPECIES
285195 Homo sapiens
331004 Mus musculus
363115 Rattus norvegicus
424772 Gallus gallus
460751 Pan troglodytes
535743 Bos taurus
611417 Canis lupus familiaris
713935 Macaca mulatta
100019120 Monodelphis domestica
100051114 Equus caballus
100410646 Callithrix jacchus
100452923 Pongo abelii
100466559 Ailuropoda melanoleuca
100489978 Xenopus (Silurana) tropicalis
100517680 Sus scrofa
Fournisseurs de qualité sélectionnés pour Solute Carrier Family 9, Subfamily A (NHE9, Cation Proton Antiporter 9), Member 9 Protéines (SLC9A9)
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