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

SLC9A9 encodes a sodium/proton exchanger that is a member of the solute carrier 9 protein family. Zusätzlich bieten wir Ihnen Solute Carrier Family 9, Subfamily A (NHE9, Cation Proton Antiporter 9), Member 9 Antikörper (65) und viele weitere Produktgruppen zu diesem Protein an.

alle Proteine anzeigen Gen GeneID UniProt
SLC9A9 285195 Q8IVB4
SLC9A9 331004 Q8BZ00
Ratte SLC9A9 SLC9A9 363115  
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Top Solute Carrier Family 9, Subfamily A (NHE9, Cation Proton Antiporter 9), Member 9 Proteine auf antikoerper-online.de

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Katalog Nr. Origin Quelle Konjugat Bilder Menge Anbieter Lieferzeit Preis Details
Insektenzellen Human rho-1D4 tag „Crystallography Grade“ protein due to multi-step, protein-specific purification process 0.5 mg Anmelden zum Anzeigen 50 bis 55 Tage
$6,041.49
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Insektenzellen Maus rho-1D4 tag „Crystallography Grade“ protein due to multi-step, protein-specific purification process 0.25 mg Anmelden zum Anzeigen 50 bis 55 Tage
$4,244.78
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Wheat germ Human GST tag 10 μg Anmelden zum Anzeigen 11 bis 12 Tage
$405.71
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SLC9A9 Proteine nach Spezies und Herkunft

Origin Exprimiert in Konjugat
Human ,
,
Mouse (Murine)

Weitere Proteine zu Solute Carrier Family 9, Subfamily A (NHE9, Cation Proton Antiporter 9), Member 9 (SLC9A9) Interaktionspartnern

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

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

  2. 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 (zeige FTL Proteine), leading to an increase in iron uptake

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

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

  5. 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.

  6. find interesting gene expression changes in endosomal NHE6 (zeige SLC9A6 Proteine) and NHE9 in postmortem autism brains.

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

  8. 33 directly measured and 13 derived glycosylation traits in 3533 individuals were identified and three novel gene association (MGAT5 (zeige MGAT5 Proteine), B3GAT1 (zeige B3GAT1 Proteine) and SLC9A9) were identified using an additional European cohort.

  9. SLC9A9 is a target gene of the BACH1 (zeige BACH1 Proteine) transcription factor according to ChIP-seq analysis in HEK (zeige EPHA3 Proteine) 293 cells.

  10. This review defines NHE6-9 as organellar NHEs that are fairly dynamic, implying that they are subjected to intracellular trafficking and thus they continuously shuttle between organelles and the plasma membrane.

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

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

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

  3. NHE9/Slc9a9 is expressed in the inner ear

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

Protein Überblick

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.

Genbezeichner und Symbole assoziert mit 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 Protein
  • 9930105B05 Protein
  • AI854429 Protein
  • AUTS16 Protein
  • Nhe9 Protein
  • RGD1560736 Protein
  • SLC9A9 Protein

Bezeichner auf Proteinebene für 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 SPEZIES
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
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