NHE-6 rabbit pAb

NHE-6 rabbit pAb

AO-06-ES4482-100

NHE-6 rabbit pAb 100μL

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Antibody Product Overview

ELK.NoES4482
Product nameNHE-6 rabbit pAb
ReactivityHuman;Mouse
ApplicationsWB;ELISA
Other nameSLC9A6; KIAA0267; NHE6; Sodium/hydrogen exchanger 6; Na(+)/H(+) exchanger 6; NHE-6; Solute carrier family 9 member 6
Size100μL
Unit price ($)248
Human gene ID10479
Human Swiss-ProtQ92581
SourceRabbit
IsotypeIgG
TargetNHE-6
Fields>>Cardiac muscle contraction
Gene nameSLC9A6
Protein nameSodium/hydrogen exchanger 6
Human gene linkView Human Gene
Human Swiss linkView Human Swiss-Prot
Mouse gene ID
Mouse gene link
Mouse Swiss-Prot
Mouse Swiss link
Rat gene ID
Rat gene link
Rat Swiss-Prot
Rat Swiss link
ImmunogenThe antiserum was produced against synthesized peptide derived from human SLC9A6. AA range:551-600
SpecificityNHE-6 Polyclonal Antibody detects endogenous levels of NHE-6 protein.
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
ClonalityPolyclonal
DilutionWestern Blot: 1/500 - 1/2000. ELISA: 1/40000. Not yet tested in other applications.
PurificationThe antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Concentration1 mg/ml
Storage stability-20°C/1 year
Molecular Weight (Da)
Observed band (KD)75kD
BackgroundThis gene encodes a sodium-hydrogen exchanger that is amember of the solute carrier family 9. The encoded protein localizes to early and recycling endosomes and may be involved in regulating endosomal pH and volume. Defects in this gene are associated with X-linked syndromic mental retardation, Christianson type. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Apr 2010],
Functioncaution:Was initially identified as a mitochondrial inner membrane protein (PubMed:9507001), but was later shown to be localized in early and recycling endosomes and not mitochondria (PubMed:11940519).,disease:Defects in SLC9A6 are the cause of mental retardation syndromic X-linked Christianson type (MRXSC) [MIM:300243]; also known as MRXS-Christianson or X-linked Angelman-like syndrome. The phenotype is characterized by profound mental retardation, epilepsy, ataxia, and microcephaly, and showed phenotypic overlap with Angelman syndrome.,function:Electroneutral exchange of protons for Na(+) and K(+) across the early and recycling endosome membranes. Contributes to calcium homeostasis.,similarity:Belongs to the monovalent cation:proton antiporter 1 (CPA1) transporter (TC 2.A.36) family.,subcellular location:Is present in the recycling compartments including early and recycling endosomes,
Subcellular locationEndosome membrane ; Multi-pass membrane protein . Is present in the recycling compartments including early and recycling endosomes, and only appears transiently on the plasma membrane.; [Isoform 2]: Recycling endosome membrane ; Multi-pass membrane protein .
ExpressionUbiquitous; but is most abundant in mitochondrion-rich tissues such as brain, skeletal muscle and heart.

Additional Images

Image 1
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Western Blot analysis of RAW cells using NHE-6 Polyclonal Antibody
Image 2
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Western blot analysis of SLC9A6 Antibody. The lane on the right is blocked with the SLC9A6 peptide.
Image 3
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Western blot analysis of the lysates from COLO205 cells using SLC9A6 antibody.
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: AO-06-ES4482-100
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Hurry! only 10 items left in stock.

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