Phone:
+1 877 302 8632
Fax:
+1 888 205 9894 (Toll-free)
E-Mail:
orders@antibodies-online.com

PTH antibody (AA 32-115)

This Mouse Monoclonal antibody specifically detects PTH in IF, FACS and IHC (p). It exhibits reactivity toward Human.
Catalog No. ABIN3024773

Quick Overview for PTH antibody (AA 32-115) (ABIN3024773)

Target

See all PTH Antibodies
PTH (Parathyroid Hormone (PTH))

Reactivity

  • 221
  • 45
  • 44
  • 42
  • 35
  • 32
  • 32
  • 32
  • 16
  • 10
  • 5
  • 2
Human

Host

  • 148
  • 107
  • 16
  • 2
Mouse

Clonality

  • 136
  • 135
Monoclonal

Conjugate

  • 167
  • 26
  • 15
  • 10
  • 6
  • 6
  • 6
  • 6
  • 6
  • 6
  • 5
  • 4
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This PTH antibody is un-conjugated

Application

  • 143
  • 87
  • 74
  • 53
  • 50
  • 43
  • 37
  • 36
  • 33
  • 26
  • 14
  • 10
  • 9
  • 7
  • 5
  • 1
  • 1
  • 1
Immunofluorescence (IF), Flow Cytometry (FACS), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Clone

PTH-1173
  • Binding Specificity

    • 35
    • 33
    • 30
    • 20
    • 17
    • 12
    • 9
    • 9
    • 8
    • 5
    • 5
    • 4
    • 4
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 32-115

    Characteristics

    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

    Immunogen

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

    Isotype

    IgG2b kappa
  • Application Notes

    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

    Preservative

    Azide free

    Storage

    4 °C,-20 °C

    Storage Comment

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

    PTH (Parathyroid Hormone (PTH))

    Alternative Name

    Parathyroid Hormone

    Target Type

    Hormone

    Background

    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
You are here:
Chat with us!