CNG-1β rabbit pAb

CNG-1β rabbit pAb

AO-06-ES2012-100

CNG-1β rabbit pAb 100μL

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Antibody Product Overview

ELK.NoES2012
Product nameCNG-1β rabbit pAb
ReactivityHuman;Mouse;Rat
ApplicationsWB;ELISA
Other nameCNGB1; CNCG2; CNCG3L; CNCG4; RCNC2; Cyclic nucleotide-gated cation channel beta-1; Cyclic nucleotide-gated cation channel 4; CNG channel 4; CNG-4; CNG4; Cyclic nucleotide-gated cation channel gamma; Cyclic nucleotide-gated cation channel mo
Size100μL
Unit price ($)248
Human gene ID1258
Human Swiss-ProtQ14028
SourceRabbit
IsotypeIgG
TargetCNG-1β
Fields>>cGMP-PKG signaling pathway;>>cAMP signaling pathway;>>Olfactory transduction;>>Phototransduction
Gene nameCNGB1
Protein nameCyclic nucleotide-gated cation channel beta-1
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 CNGB1. AA range:571-620
SpecificityCNG-1β Polyclonal Antibody detects endogenous levels of CNG-1β protein.
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
ClonalityPolyclonal
DilutionWestern Blot: 1/500 - 1/2000. ELISA: 1/10000. 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)102kD
BackgroundIn humans, the rod photoreceptor cGMP-gated cation channel helps regulate ion flow into the rod photoreceptor outer segment in response to light-induced alteration of the levels of intracellular cGMP. This channel consists of two subunits, alpha and beta, with the protein encoded by this gene representing the beta subunit. Defects in this gene are a cause of cause of retinitis pigmentosa type 45. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2013],
Functiondisease:Defects in CNGB1 are the cause of retinitis pigmentosa type 25 (RP25) [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.,similarity:Belongs to the cyclic nucleotide-gated cation channel (TC 1.A.1.5) family.,similarity:Contains 1 cyclic nucleotide-binding domain.,subunit:Heterooligomeric complex with CNGA1.,
Subcellular locationMembrane; Multi-pass membrane protein.
ExpressionRetina,

Additional Images

Image 1
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Western Blot analysis of various cells using CNG-1β Polyclonal Antibody
Image 2
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Western Blot analysis of 3T3 cells using CNG-1β Polyclonal Antibody
Image 3
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Western blot analysis of lysates from NIH/3T3 and A549 cells, using CNGB1 Antibody. The lane on the right is blocked with the synthesized peptide.
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: AO-06-ES2012-100
: 10 Items
Hurry! only 10 items left in stock.

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