catalog number :
MBS211854
products full name :
MOUSE ANTI PARATHYROID HORMONE
products short name :
PARATHYROID HORMONE
other names :
parathyroid hormone preproprotein; Parathyroid hormone; parathyroid hormone; parathormone; parathyrin; parathyroid hormone 1; prepro-PTH; preproparathyroid hormone; parathyroid hormone; Parathormone; Parathyrin
other gene names :
PTH; PTH; PTH1; PTH
uniprot entry name :
PTHY_HUMAN
specificity :
This item reacts with human parathyroid hormone (PTH), a secreted peptide involved in calcium homeostasis. This antibody has not been cross-adsorbed and may react with homologous proteins from related species.
form :
Purified. Purified IgG - liquid
concentration :
IgG concentration 1.0 mg/ml
storage stability :
Store at 4 degree C or at -20 degree C if preferred. Storage in frost-free freezers is not recommended. This product should be stored undiluted. Avoid repeated freezing and thawing as this may denature the antibody. Should this product contain a precipitate we recommend microcentrifugation before use. Shelf Life: 18 months from date of despatch.
tested application :
ELISA (EIA), Immunohistology Paraffin, Radioimmunoassays (RIA)
other info1 :
Perservative Stabilisers: 0.09% Sodium Azide (NaN3) . Preparation: Purified IgG prepared by affinity chromatography on Protein G
other info2 :
Immunogen: Synthetic peptide corresponding to amino acids 1 to 34 of mature human parathyroid hormone (PTH) conjugated to a proprietary carrier molecule. Buffer Solution: Phosphate buffered saline. Affinity: 5 x 108 with 1-34 PTH
. 2 x 107 with 1-84 PTH. Target Species: Human
products description :
MBS211854 reacts with human parathyroid hormone (PTH), a secreted peptide involved in calcium homeostasis. This antibody has not been cross-adsorbed and may react with homologous proteins from related species.
ncbi acc num :
NP_000306.1
ncbi gb acc num :
NM_000315.2
ncbi mol weight :
12,861 Da
ncbi pathways :
Class B/2 (Secretin Family Receptors) Pathway 106378!!Defective ACTH Causes Obesity And Pro-opiomelanocortinin Deficiency (POMCD) Pathway 1127664!!Disease Pathway 530764!!Endochondral Ossification Pathway 198812!!G Alpha (s) Signalling Events Pathway 119549!!GPCR Downstream Signaling Pathway 119548!!GPCR Ligand Binding Pathway 161020!!Metabolic Disorders Of Biological Oxidation Enzymes Pathway 1127637!!Osteoblast Signaling Pathway 198842!!Signal Transduction Pathway 477114
ncbi summary :
The protein encoded by this gene is a hormone secreted by parathyroid cells. This hormone elevates blood Ca2+ level by dissolving the salts in bone and preventing their renal excretion. Defects in this gene are a cause of familial isolated hypoparathyroidism (FIH). [provided by RefSeq, Jul 2008]