Cell Biology Antibodies 9
Anti-PTH Antibody (CAB5846)
- SKU:
- CAB5846
- Product Type:
- Antibody
- Reactivity:
- Human
- Host Species:
- Rabbit
- Isotype:
- IgG
- Antibody Type:
- Polyclonal Antibody
- Research Area:
- Cell Biology
Description
| Antibody Name: | Anti-PTH Antibody |
| Antibody SKU: | CAB5846 |
| Antibody Size: | 20uL, 50uL, 100uL |
| Application: | WB IF |
| Reactivity: | Human |
| Host Species: | Rabbit |
| Immunogen: | Recombinant fusion protein containing a sequence corresponding to amino acids 20-115 of human PTH (NP_000306.1). |
| Application: | WB IF |
| Recommended Dilution: | WB 1:500 - 1:2000 IF 1:10 - 1:100 |
| Reactivity: | Human |
| Positive Samples: | U-251MG, 293T |
| Immunogen: | Recombinant fusion protein containing a sequence corresponding to amino acids 20-115 of human PTH (NP_000306.1). |
| Purification Method: | Affinity purification |
| Storage Buffer: | Store at -20'C. Avoid freeze / thaw cycles. Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3. |
| Isotype: | IgG |
| Sequence: | LTKS DGKS VKKR SVSE IQLM HNLG KHLN SMER VEWL RKKL QDVH NFVA LGAP LAPR DAGS QRPR KKED NVLV ESHE KSLG EADK ADVN VLTK AKSQ |
| Gene ID: | 5741 |
| Uniprot: | P01270 |
| Cellular Location: | Secreted |
| Calculated MW: | 12kDa |
| Observed MW: | 14kDa |
| Synonyms: | PTH, PTH1 |
| Background: | This gene encodes a member of the parathyroid family of proteins. The encoded preproprotein is proteolytically processed to generate a protein that binds to the parathyroid hormone/parathyroid hormone-related peptide receptor and regulates blood calcium and phosphate levels. Excess production of the encoded protein, known as hyperparathyroidism, can result in hypercalcemia and kidney stones. On the other hand, defective processing of the encoded protein may lead to hypoparathyroidism, which can result in hypocalcemia and numbness. Alternative splicing results in multiple transcript variants. |
| UniProt Protein Function: | PTH: PTH elevates calcium level by dissolving the salts in bone and preventing their renal excretion. Stimulates [1-14C]-2- deoxy-D-glucose (2DG) transport and glycogen synthesis in osteoblastic cells. Defects in PTH 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. Belongs to the parathyroid hormone family. |
| UniProt Protein Details: | Protein type:Secreted, signal peptide; Secreted; Hormone; Apoptosis Chromosomal Location of Human Ortholog: 11p15.3-p15.1 Cellular Component: extracellular space; extracellular region Molecular Function:RNA polymerase II transcription factor activity, enhancer binding; type 1 parathyroid hormone receptor binding; parathyroid hormone receptor binding; peptide hormone receptor binding; hormone activity Biological Process: response to drug; transcription from RNA polymerase II promoter; positive regulation of signal transduction; induction of apoptosis by hormones; positive regulation of glycogen biosynthetic process; negative regulation of transcription from RNA polymerase II promoter; positive regulation of bone mineralization; G-protein signaling, adenylate cyclase activating pathway; Rho protein signal transduction; cellular calcium ion homeostasis; positive regulation of glucose import; G-protein coupled receptor protein signaling pathway; cAMP metabolic process; response to vitamin D; response to cadmium ion; response to ethanol; cell-cell signaling; regulation of gene expression; positive regulation of cAMP biosynthetic process; response to lead ion; positive regulation of transcription from RNA polymerase II promoter; skeletal development; bone resorption Disease: Hypoparathyroidism, Familial Isolated |
| 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] |
| UniProt Code: | P01270 |
| NCBI GenInfo Identifier: | 131547 |
| NCBI Gene ID: | 5741 |
| NCBI Accession: | P01270.1 |
| UniProt Secondary Accession: | P01270,Q4VB48, Q9UD38, |
| UniProt Related Accession: | P01270 |
| Molecular Weight: | 12,861 Da |
| NCBI Full Name: | Parathyroid hormone |
| NCBI Synonym Full Names: | parathyroid hormone |
| NCBI Official Symbol: | PTH |
| NCBI Official Synonym Symbols: | PTH1 |
| NCBI Protein Information: | parathyroid hormone; parathyrin; prepro-PTH; parathormone; parathyroid hormone 1; preproparathyroid hormone |
| UniProt Protein Name: | Parathyroid hormone |
| UniProt Synonym Protein Names: | Parathormone; Parathyrin |
| Protein Family: | Parathyroid hormone |
| UniProt Gene Name: | PTH |
| UniProt Entry Name: | PTHY_HUMAN |
 | Western blot analysis of extracts of various cell lines, using PTH antibody (CAB5846) at 1:1000 dilution. Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) (CABS014) at 1:10000 dilution. Lysates/proteins: 25ug per lane. Blocking buffer: 3% nonfat dry milk in TBST. Detection: ECL Enhanced Kit (RM00021). Exposure time: 60s. |
 | Immunofluorescence analysis of U2OS cells using PTH antibody (CAB5846). Blue: DAPI for nuclear staining. |
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