Synphilin-1 rabbit pAb

Synphilin-1 rabbit pAb

AO-06-ES3536-100

Synphilin-1 rabbit pAb 100μL

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Antibody Product Overview

ELK.NoES3536
Product nameSynphilin-1 rabbit pAb
ReactivityHuman;Mouse
ApplicationsWB;IHC;IF;ELISA
Other nameSNCAIP; Synphilin-1; Sph1; Alpha-synuclein-interacting protein
Size100μL
Unit price ($)248
Human gene ID9627
Human Swiss-ProtQ9Y6H5
SourceRabbit
IsotypeIgG
TargetSynphilin-1
Fields>>Parkinson disease;>>Pathways of neurodegeneration - multiple diseases
Gene nameSNCAIP
Protein nameSynphilin-1
Human gene linkView Human Gene
Human Swiss linkView Human Swiss-Prot
Mouse gene ID
Mouse gene link
Mouse Swiss-ProtQ99ME3
Mouse Swiss linkView Mouse Swiss-Prot
Rat gene ID
Rat gene link
Rat Swiss-Prot
Rat Swiss link
ImmunogenThe antiserum was produced against synthesized peptide derived from human Synphilin-1. AA range:797-846
SpecificitySynphilin-1 Polyclonal Antibody detects endogenous levels of Synphilin-1 protein.
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
ClonalityPolyclonal
DilutionWestern Blot: 1/500 - 1/2000. Immunohistochemistry: 1/100 - 1/300. 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)100kD
BackgroundThis gene encodes a protein containing several protein-protein interaction domains, including ankyrin-like repeats, a coiled-coil domain, and an ATP/GTP-binding motif. The encoded protein interacts with alpha-synuclein in neuronal tissue and may play a role in the formation of cytoplasmic inclusions and neurodegeneration. A mutation in this gene has been associated with Parkinson's disease. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2015],
Functiondisease:Defects in SNCAIP are a cause of Parkinson disease (PD) [MIM:168600]. PD is a complex, multifactorial disorder that typically manifests after the age of 50 years, although early-onset cases (before 50 years) are known. PD generally arises as a sporadic condition but is occasionally inherited as a simple mendelian trait. Although sporadic and familial PD are very similar, inherited forms of the disease usually begin at earlier ages and are associated with atypical clinical features. PD is characterized by bradykinesia, resting tremor, muscular rigidity and postural instability, as well as by a clinically significant response to treatment with levodopa. The pathology involves the loss of dopaminergic neurons in the substantia nigra and the presence of Lewy bodies (intraneuronal accumulations of aggregated proteins), in surviving neurons in various areas of the brain.,miscellaneous:
Subcellular locationCytoplasm . Detected in cytoplasmic inclusion bodies, together with SNCA.
ExpressionDetected in brain (at protein level). Widely expressed, with highest levels in brain, heart and placenta.

Additional Images

Image 1
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Western Blot analysis of various cells using Synphilin-1 Polyclonal Antibody
Image 2
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Immunohistochemical analysis of paraffin-embedded Human lung cancer. Antibody was diluted at 1:100(4° overnight). High-pressure and temperature Tris-EDTA,pH8.0 was used for antigen retrieval. Negetive contrl (right) obtaned from antibody was pre-absorbed by immunogen peptide.
Image 3
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Immunohistochemistry analysis of Synphilin-1 antibody in paraffin-embedded lung carcinoma. tissue.
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Western blot analysis of lysate from COLO205, using Synphilin-1 antibody.
: AO-06-ES3536-100
: 10 Items
Hurry! only 10 items left in stock.

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