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PTH Antikörper

Der Maus Monoklonal anti-PTH Antikörper wird verwendet zum Nachweis von PTH in Proben von Human. Er wurde validiert für IHC (p).
Produktnummer ABIN3024768
642,40 €
Zzgl. Versandkosten 20,00 € und MwSt
Lieferung nach: Deutschland
Lieferung in 6 bis 9 Werktagen

Kurzübersicht für PTH Antikörper (ABIN3024768)

Target

Alle PTH Antikörper anzeigen
PTH (Parathyroid Hormone (PTH))

Reaktivität

  • 224
  • 41
  • 37
  • 35
  • 32
  • 30
  • 30
  • 30
  • 15
  • 7
  • 5
  • 2
Human

Wirt

  • 142
  • 101
  • 11
  • 2
  • 1
Maus

Klonalität

  • 140
  • 115
Monoklonal

Konjugat

  • 154
  • 23
  • 12
  • 6
  • 6
  • 6
  • 6
  • 6
  • 6
  • 6
  • 4
  • 4
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Dieser PTH Antikörper ist unkonjugiert

Applikation

  • 134
  • 73
  • 68
  • 41
  • 34
  • 33
  • 33
  • 26
  • 22
  • 15
  • 10
  • 9
  • 8
  • 4
  • 2
  • 1
  • 1
  • 1
Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Klon

3H9
  • Verwendungszweck

    Parathyroid Hormone Antibody / N-Terminal

    Produktmerkmale

    Epitope of this mAb maps in between aa 1-34. PTH is 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.

    Aufreinigung

    Protein G affinity chromatography

    Immunogen

    Synthetic peptide corresponding to amino acids 1 to 34 of mature PTH was used as the immunogen for the Parathyroid Hormone antibody.

    Isotyp

    IgG2b, kappa
  • Applikationshinweise

    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.

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Konzentration

    0.2 mg/mL

    Buffer

    0.2 mg/mL in 1X PBS with 0.1 mg/mL BSA (US sourced) and 0.05 % sodium azide

    Konservierungsmittel

    Sodium azide

    Vorsichtsmaßnahmen

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

    Lagerung

    4 °C,-20 °C

    Informationen zur Lagerung

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

    PTH (Parathyroid Hormone (PTH))

    Andere Bezeichnung

    Parathyroid Hormone

    Substanzklasse

    Hormone

    Hintergrund

    PTH is 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.

    UniProt

    P01270

    Pathways

    cAMP Metabolic Process, Regulation of Carbohydrate Metabolic Process
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