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Huntingtin anticorps (pSer421)

L’anticorps Lapin Polyclonal anti-Huntingtin a été validé pour IHC, WB et ELISA. Il convient pour détecter Huntingtin dans des échantillons de Humain.
Rockland
N° du produit ABIN100604
N° du produit (Fournisseur): 600-401-433

Aperçu rapide pour Huntingtin anticorps (pSer421) (ABIN100604)

Antigène

Voir toutes Huntingtin (HTT) Anticorps
Huntingtin (HTT)

Reactivité

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  • 1
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Humain

Hôte

  • 57
  • 24
  • 2
Lapin

Clonalité

  • 49
  • 33
Polyclonal

Conjugué

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Cet anticorp Huntingtin est non-conjugé

Application

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Immunohistochemistry (IHC), Western Blotting (WB), ELISA
  • Épitope

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    pSer421

    N° du produit (Fournisseur)

    600-401-433

    Fournisseur

    Rockland

    Fonction

    Huntington phospho S421 Antibody

    Réactivité croisée (Details)

    This antibody is specific for phosphorylated human Huntington protein at the pS421 residue.

    Attributs du produit

    Synonyms: rabbit anti-Huntington pS421 antibody, rabbit anti-Huntingtin pS421 antibody, HD protein, HTT, Huntington Disease Protein, Huntington disease, IT15, LOMARS

    Purification

    Anti-Huntingtin pS421 is an affinity purified antibody produced by immunoaffinity chromatography using phospho peptide coupled to agarose beads followed by solid phase adsorption(s) against non-phospho peptide and non-specific peptide to remove any unwanted reactivities.

    Stérilité

    Sterile filtered

    Immunogène

    Immunogen: Huntingtin pS421 Antibody was prepared from whole rabbit serum produced by repeated immunizations with a synthetic peptide corresponding to an internal region near aa 400-425 of Human Huntington Disease Protein.

    Immunogen Type: Conjugated Peptide

    Isotype

    IgG
  • Indications d'application

    Immunohistochemistry Dilution: 1:50 - 1:100

    Application Note: Anti-Huntingtin pS421 antibody has been tested for use in ELISA, immunohistochemistry, and by western blot.  Specific conditions for reactivity should be optimized by the end user. Expect bands at approximately 350 kDa and 200 kDa in size corresponding to full-length Huntingtin protein and truncated (hypothetical) Huntingtin protein, respectively, by western blotting in the appropriate cell lysate or extract.   This antibody is specific for the phosphorylated form of Huntingtin protein at the pS421 residue.  The identity of lower molecular bands ~130 kDa is not known.

    Western Blot Dilution: 1:500 - 1:3,000

    ELISA Dilution: 1:10,000 - 1:40,000

    Other: User Optimized

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.6 mg/mL

    Buffer

    Buffer: 0.02 M Potassium Phosphate, 0.15 M Sodium Chloride, pH 7.2

    Stabilizer: None

    Preservative: 0.01 % (w/v) Sodium Azide

    Agent conservateur

    Sodium azide

    Précaution d'utilisation

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Stock

    4 °C,-20 °C

    Stockage commentaire

    Store vial at -20° C prior to opening. Aliquot contents and freeze at -20° C or below for extended storage. Avoid cycles of freezing and thawing. Centrifuge product if not completely clear after standing at room temperature. This product is stable for several weeks at 4° C as an undiluted liquid. Dilute only prior to immediate use.

    Date de péremption

    12 months
  • Antigène

    Huntingtin (HTT)

    Autre désignation

    HTT

    Sujet

    Background: Huntingtin (also known as Huntington's disease protein, Htt and HD protein) is the protein product of a disease gene linked to Huntington's disease, a neuro-degenerative disorder characterized by loss of striatal neurons. This may be caused by an expanded, unstable trinucleotide repeat in the huntingtin gene, which translates as a polyglutamine repeat in the protein product (see partial protein sequence below). The huntingtin gene locus is large, spanning 180 kb and consisting of 67 exons.  It is expressed as 2 alternatively polyadenylated forms displaying different relative abundance in various fetal and adult tissues. The genetic defect leading to Huntington's disease may not necessarily eliminate transcription, but may confer a new property on the mRNA or alter the function of the protein. One candidate is the huntingtin-associated protein-1, highly expressed in brain, which has increased affinity for huntingtin protein with expanded polyglutamine repeats. Normal huntingtin protein shows a cytoplasmic localization.  This protein is widely expressed with the highest level of expression in the brain (nerve fibers, varicosities, and nerve endings). In the brain, the regions where it can be mainly found are the cerebellar cortex, the neocortex, the striatum, and the hippocampal formation.

    ID gène

    3064

    NCBI Accession

    NP_002102

    UniProt

    P42858

    Pathways

    Signalisation PI3K-Akt, Hormone Transport, Transition Metal Ion Homeostasis, Tube Formation, Protein targeting to Nucleus, Dicarboxylic Acid Transport
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