CNG-1 rabbit pAb

CNG-1 rabbit pAb

AO-06-ES4717-100

CNG-1 rabbit pAb 100μL

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Antibody Product Overview

ELK.NoES4717
Product nameCNG-1 rabbit pAb
ReactivityHuman;Mouse;Rat
ApplicationsWB;ELISA
Other nameCNGA1; CNCG; CNCG1; cGMP-gated cation channel alpha-1; Cyclic nucleotide-gated cation channel 1; Cyclic nucleotide-gated channel alpha-1; CNG channel alpha-1; CNG-1; CNG1; Cyclic nucleotide-gated channel; photoreceptor; Rod photoreceptor cG
Size100μL
Unit price ($)248
Human gene ID1259
Human Swiss-ProtP29973
SourceRabbit
IsotypeIgG
TargetCNG-1
Fields>>cGMP-PKG signaling pathway;>>cAMP signaling pathway;>>Phototransduction
Gene nameCNGA1
Protein namecGMP-gated cation channel alpha-1
Human gene linkView Human Gene
Human Swiss linkView Human Swiss-Prot
Mouse gene ID12788
Mouse gene linkView Mouse Gene
Mouse Swiss-ProtP29974
Mouse Swiss linkView Mouse Swiss-Prot
Rat gene ID85259
Rat gene linkView Rat Gene
Rat Swiss-ProtQ62927
Rat Swiss linkView Rat Swiss-Prot
ImmunogenThe antiserum was produced against synthesized peptide derived from human CNGA1. AA range:401-450
SpecificityCNG-1 Polyclonal Antibody detects endogenous levels of CNG-1 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)80kD
BackgroundThe protein encoded by this gene is involved in phototransduction. Along with another protein, the encoded protein forms a cGMP-gated cation channel in the plasma membrane, allowing depolarization of rod photoreceptors. This represents the last step in the phototransduction pathway. Defects in this gene are a cause of retinitis pigmentosa autosomal recessive (ARRP) disease. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2008],
Functioncaution:It is uncertain whether Met-1 or Met-5 is the initiator.,disease:Defects in CNGA1 are a cause of retinitis pigmentosa autosomal recessive (ARRP) [MIM:268000]. RP leads to degeneration of retinal photoreceptor cells. Patients typically have night vision blindness and loss of midperipheral visual field. As their condition progresses, they lose their far peripheral visual field and eventually central vision as well.,function:Visual signal transduction is mediated by a G-protein coupled cascade using cGMP as second messenger. This protein can be activated by cyclic GMP which leads to an opening of the cation channel and thereby causing a depolarization of rod photoreceptors.,online information:Retina International's Scientific Newsletter,similarity:Belongs to the cyclic nucleotide-gated cation channel (TC 1.A.1.5) family.,similarity:Contains 1 cyclic nucleotide-binding domain.,subuni
Subcellular locationCell membrane ; Multi-pass membrane protein .
ExpressionRod cells in the retina.

Additional Images

Image 1
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Western Blot analysis of HepG2 cells using CNG-1 Polyclonal Antibody
Image 2
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Western blot analysis of CNGA1 Antibody. The lane on the right is blocked with the CNGA1 peptide.
Image 3
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Western blot analysis of the lysates from HepG2 cells using CNGA1 antibody.
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: AO-06-ES4717-100
: 10 Items
Hurry! only 10 items left in stock.

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