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HSP27 anticorps (AA 1-205)

L’anticorps anti-HSP27 Polyclonal Lapin est utilisé pour la détection de HSP27 dans des échantillons de Humain. Il a été validé pour WB, IHC, IF, FACS, IP, ICC et IHC (fro).
N° du produit ABIN3042464
500,50 €
Plus frais de livraison 40,00 € et TVA
100 μg
Destination: France
Envoi sous 8 à 12 jours ouvrables

Aperçu rapide pour HSP27 anticorps (AA 1-205) (ABIN3042464)

Antigène

Voir toutes HSP27 (HSPB1) Anticorps
HSP27 (HSPB1) (Heat Shock 27kDa Protein 1 (HSPB1))

Reactivité

  • 370
  • 137
  • 122
  • 35
  • 25
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  • 11
  • 9
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  • 1
  • 1
Humain

Hôte

  • 282
  • 96
Lapin

Clonalité

  • 210
  • 167
Polyclonal

Conjugué

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  • 26
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Cet anticorp HSP27 est non-conjugé

Application

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Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF), Flow Cytometry (FACS), Immunoprecipitation (IP), Immunocytochemistry (ICC), Immunohistochemistry (Frozen Sections) (IHC (fro))
  • Épitope

    • 52
    • 47
    • 32
    • 16
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    • 8
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    AA 1-205

    Fonction

    Anti-Hsp27/HSPB1 Antibody

    Réactivité croisée (Details)

    No cross-reactivity with other proteins

    Attributs du produit

    Anti-Hsp27/HSPB1 Antibody (ABIN3042464). Tested in Flow Cytometry, IP, IF, IHC, IHC-F, ICC, WB applications. This antibody reacts with Human. This is a premium antibody that guarantees superior quality, high affinity, and strong signals with minimal background in Western blot applications.

    Purification

    Immunogen affinity purified.

    Immunogène

    E.coli-derived human Hsp27 recombinant protein (Position: M1-K205). Human Hsp27 shares 83% amino acid (aa) sequence identity with mouse Hsp27.

    Isotype

    IgG
  • Indications d'application

    Western blot, 0.1-0.5 μg/mL, Human
    Immunohistochemistry (Paraffin-embedded Section), 0.5-1 μg/mL, Human
    Immunohistochemistry (Frozen Section), 0.5-1 μg/mL, Human, -
    Immunocytochemistry/Immunofluorescence, 2 μg/mL, Human, -
    Immunoprecipitation, 0.5-2 μg/mL, Human
    Flow Cytometry (Fixed), 1-3 μg/mLx106 cells, Human, -

    Commentaires

    Antibody can be supported by chemiluminescence kit ABIN921124 in WB, supported by ABIN921231 in IHC(P) and IHC(F).

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Add 0.2 mL of distilled water will yield a concentration of 500 μg/mL.

    Concentration

    500 μg/mL

    Buffer

    Each vial contains 5 mg BSA, 0.9 mg NaCl, 0.2 mg Na2HPO4, 0.01 mg 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.

    Conseil sur la manipulation

    Avoid repeated freezing and thawing.

    Stock

    4 °C,-20 °C

    Stockage commentaire

    Store at -20°C for one year from date of receipt. After reconstitution, at 4°C for one month.
    It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freeze-thaw cycles.
  • Antigène

    HSP27 (HSPB1) (Heat Shock 27kDa Protein 1 (HSPB1))

    Autre désignation

    HSPB1

    Sujet

    Synonyms: Heat shock protein beta-1,HspB1,28 kDa heat shock protein,Estrogen-regulated 24 kDa protein,Heat shock 27 kDa protein,HSP 27,Stress-responsive protein 27,SRP27,HSPB1,HSP27, HSP28,

    Tissue Specificity: Detected in all tissues tested: skeletal muscle, heart, aorta, large intestine, small intestine, stomach, esophagus, bladder, adrenal gland, thyroid, pancreas, testis, adipose tissue, kidney, liver, spleen, cerebral cortex, blood serum and cerebrospinal fluid. Highest levels are found in the heart and in tissues composed of striated and smooth muscle. .

    Background: HSPB1 (Heat shock 27 kDa protein 1), also known as HSP27, is a protein that in humans is encoded by the HSPB1 gene. HSP27 gene is mapped to 7q11.23. The protein encoded by this gene is induced by environmental stress and developmental changes. The encoded protein is involved in stress resistance and actin organization and translocates from the cytoplasm to the nucleus upon stress induction. Defects in this gene are a cause of Charcot-Marie-Tooth disease type 2F (CMT2F) and distal hereditary motor neuropathy (dHMN).

    Sequence Similarities: Belongs to the small heat shock protein (HSP20) family.

    Poids moléculaire

    27 kDa

    ID gène

    3315

    UniProt

    P04792

    Pathways

    Signalisation MAPK, Regulation of Actin Filament Polymerization, Signaling Events mediated by VEGFR1 and VEGFR2, Negative Regulation of intrinsic apoptotic Signaling, VEGF Signaling
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