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beta Synuclein (ready-to-use)

ArtNr 18-272-196448
Hersteller GENWAY
Menge 7 ml
Kategorie
Typ Antibody
Applikationen IHC
Specific against other
ECLASS 10.1 32160702
ECLASS 11.0 32160702
UNSPSC 12352203
Alias GWB-96DD67
Similar products 18-272-196448
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Genway ID:
GWB-96DD67
Isotype:
IgG
Immunogen:
Synthetic peptide (unfortunately the amino acid sequence is considered to be commercially sensitive) (Human) (C terminal).
Antigen Species:
Human
Specificity:
This antibody is specific for beta synuclein and does not cross react withalpha or gamma synuclein. Stains neuronal cytosol and presynaptic terminals.
Positive Control:
Brain.
Target:
beta Synuclein
Localization:
Cytoplasmic Storage
Buffer:
PBS pH 7. 4 containing 1%BSA and 0. 1% sodium azide
Application Note:
IHC-P: Ready to use for 10 minutes at room temperature. No special pretreatment is required for the immunohistochemical staining of formalin/paraffin tissues. Not tested in other applications. Optimal dilutions/concentrations should be determined by the end user. Cellular
Localization:
Cytoplasmic Synucleins are small soluble proteins expressed primarily in neural tissue and in certain tumors. The family includes three known proteins: alpha synuclein beta synuclein and gamma synuclein. The alpha and beta synuclein proteins are found primarily in brain tissue where they are seen mainly in presynaptic terminals.
Function:
Non-amyloid component of senile plaques found in Alzheimer disease. Could act as a regulator of SNCA aggregation process. Protects neurons from staurosporine and 6 hydroxy dopamine (6OHDA)-stimulated caspase activation in a p53-dependent manner. Contributes to restore the SNCA anti-apoptotic function abolished by 6OHDA. Not found in the Lewy bodies associated with Parkinson disease.
Subcellular Location:
Cytoplasm.
Tissue Specificity:
Expressed predominantly in brain; concentrated in presynaptic nerve terminals.
Ptm:
Phosphorylated. Phosphorylation by G-protein coupled receptor kinases (GRK) is more efficient than phosphorylation by CK1 CK2 and CaM-kinase II.
Disease:
Brain iron accumulation type 1 (NBIA1 also called Hallervorden-Spatz syndrome) a rare neuroaxonal dystrophy is histologically characterized by axonal spheroids iron deposition Lewy body (LB)-like intraneuronal inclusions glial inclusions and neurofibrillary tangles. SNCB is found in spheroids but not in inclusions.
Similarity:
Belongs to the synuclein family.

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Alle Produkte sind nur für Forschungszwecke bestimmt. Nicht für den menschlichen, tierärztlichen oder therapeutischen Gebrauch.

Menge: 7 ml
Lieferbar: In stock
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