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PTH anticorps (AA 32-115)

Cet anticorps Souris Monoclonal détecte spécifiquement PTH dans IF, FACS et IHC (p). Il présente une réactivité envers Humain.
N° du produit ABIN3024773

Aperçu rapide pour PTH anticorps (AA 32-115) (ABIN3024773)

Antigène

Voir toutes PTH Anticorps
PTH (Parathyroid Hormone (PTH))

Reactivité

  • 216
  • 42
  • 40
  • 39
  • 35
  • 32
  • 32
  • 32
  • 14
  • 7
  • 5
  • 2
Humain

Hôte

  • 133
  • 100
  • 16
  • 4
Souris

Clonalité

  • 130
  • 121
Monoclonal

Conjugué

  • 158
  • 23
  • 12
  • 6
  • 6
  • 6
  • 6
  • 6
  • 6
  • 6
  • 4
  • 4
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp PTH est non-conjugé

Application

  • 117
  • 72
  • 66
  • 51
  • 43
  • 33
  • 33
  • 29
  • 26
  • 18
  • 14
  • 10
  • 9
  • 5
  • 4
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Immunofluorescence (IF), Flow Cytometry (FACS), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Clone

PTH-1173
  • Épitope

    • 35
    • 34
    • 28
    • 17
    • 17
    • 12
    • 11
    • 8
    • 6
    • 6
    • 5
    • 4
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 32-115

    Attributs du produit

    Epitope of this mAb maps in the C-terminus of PTH, a hormone produced by the parathyroid gland that regulates the concentration of calcium and phosphorus in extracellular fluid. This hormone elevates blood Ca2+ levels by dissolving the salts in bone and preventing their renal excretion. It is produced in the parathyroid gland as an 84 amino acid single chain polypeptide. It can also be secreted as N-terminal truncated fragments or C-terminal fragments after intracellular degradation, as in case of hypercalcemia. Defects in this gene are a cause of familial isolated hypoparathyroidism (FIH), also called autosomal dominant hypoparathyroidism or autosomal dominant hypocalcemia. FIH is characterized by hypocalcemia and hyperphosphatemia due to inadequate secretion of parathyroid hormone. Symptoms are seizures, tetany and cramps. FIH exist both as autosomal dominant and recessive forms of hypoparathyroidism.

    Purification

    Protein G affinity chromatography

    Immunogène

    Amino acids 32-115 of human PTH was used as the immunogen for the Parathyroid Hormone antibody.

    Isotype

    IgG2b kappa
  • Indications d'application

    Optimal dilution of the Parathyroid Hormone antibody should be determined by the researcher.

    1. Staining of formalin-fixed tissues requires boiling tissue sections in 10  mM Citrate buffer,  pH 6.0, for 10-20 min followed by cooling at RT for 20 min.
    2. The prediluted format is supplied in a dropper bottle and is optimized for use in IHC. After epitope retrieval step (if required), drip mAb solution onto the tissue section and incubate at RT for 30 min.\. Flow Cytometry: 0.5-1 μg/million cells in 0.1ml,Immunofluorescence: 0.5-1 μg/mL,Immunohistochemistry (FFPE): 0.5-1 μg/mL for 30 min at RT (1),Prediluted format: incubate for 30 min at RT (2)

    Restrictions

    For Research Use only
  • Concentration

    1 mg/mL

    Buffer

    1 mg/mL in 1X PBS, BSA free, sodium azide free

    Agent conservateur

    Azide free

    Stock

    4 °C,-20 °C

    Stockage commentaire

    Store the Parathyroid Hormone antibody at 2-8°C (with azide) or aliquot and store at -20°C or colder (without azide).
  • Antigène

    PTH (Parathyroid Hormone (PTH))

    Autre désignation

    Parathyroid Hormone

    Classe de substances

    Hormone

    Sujet

    Epitope of this mAb maps in the C-terminus of PTH, a hormone produced by the parathyroid gland that regulates the concentration of calcium and phosphorus in extracellular fluid. This hormone elevates blood Ca2+ levels by dissolving the salts in bone and preventing their renal excretion. It is produced in the parathyroid gland as an 84 amino acid single chain polypeptide. It can also be secreted as N-terminal truncated fragments or C-terminal fragments after intracellular degradation, as in case of hypercalcemia. Defects in this gene are a cause of familial isolated hypoparathyroidism (FIH), also called autosomal dominant hypoparathyroidism or autosomal dominant hypocalcemia. FIH is characterized by hypocalcemia and hyperphosphatemia due to inadequate secretion of parathyroid hormone. Symptoms are seizures, tetany and cramps. FIH exist both as autosomal dominant and recessive forms of hypoparathyroidism.

    Pathways

    cAMP Metabolic Process, Regulation of Carbohydrate Metabolic Process
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