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

SLC9A9 encodes a sodium/proton exchanger that is a member of the solute carrier 9 protein family. Additionally we are shipping Solute Carrier Family 9, Subfamily A (NHE9, Cation Proton Antiporter 9), Member 9 Antibodies (64) and many more products for this protein.

list all proteins Gene Name GeneID UniProt
SLC9A9 285195 Q8IVB4
SLC9A9 331004 Q8BZ00
Rat SLC9A9 SLC9A9 363115  
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Top Solute Carrier Family 9, Subfamily A (NHE9, Cation Proton Antiporter 9), Member 9 Proteins at antibodies-online.com

Showing 3 out of 3 products:

Catalog No. Origin Source Conjugate Images Quantity Supplier Delivery Price Details
Insect Cells Human rho-1D4 tag „Crystallography Grade“ protein due to multi-step, protein-specific purification process 0.5 mg Log in to see 50 to 55 Days
$6,041.49
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Insect Cells Mouse rho-1D4 tag „Crystallography Grade“ protein due to multi-step, protein-specific purification process 0.25 mg Log in to see 50 to 55 Days
$4,244.78
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HOST_Wheat germ Human GST tag 10 μg Log in to see 11 to 12 Days
$405.71
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SLC9A9 Proteins by Origin and Source

Origin Expressed in Conjugate
Human ,
,
Mouse (Murine)

More Proteins for Solute Carrier Family 9, Subfamily A (NHE9, Cation Proton Antiporter 9), Member 9 (SLC9A9) Interaction Partners

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

  1. SLC9A9 has an oncogenic function by being related to EGFR (show EGFR Proteins) 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 (show FTL Proteins), 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 (show SLC9A6 Proteins) 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 (show MGAT5 Proteins), B3GAT1 (show B3GAT1 Proteins) and SLC9A9) were identified using an additional European cohort.

  9. SLC9A9 is a target gene of the BACH1 (show BACH1 Proteins) transcription factor according to ChIP-seq analysis in HEK (show EPHA3 Proteins) 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) interaction partners

  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 Profile

Protein Summary

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

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
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