Alkaline Phosphatase, Tissue-Nonspecific Isozyme (ALPL) Antibody
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935106861
info@markelab.com
Precio
292.5€ (80 µl)
Antibody anti-ALPL
proveedor
Abbexareference
abx028274Tested Applications
ELISA, WB, IHC, IF/ICC, FCMreactivity
Human, Mousestatus
RUOclonality
PolyclonalDescripción
Alkaline Phosphatase, Tissue-Nonspecific Isozyme (ALPL) Antibody is a rabbit polyclonal antibody for ALPL. There are at least four distinct but related alkaline phosphatases: intestinal, placental, placental-like, and liver/bone/kidney (tissue non-specific). This protein is a membrane bound glycosylated enzyme that is not expressed in any particular tissue and is, therefore, referred to as the tissue-nonspecific form of the enzyme. The exact physiological function of the alkaline phosphatases is not known. A proposed function of this form of the enzyme is matrix mineralization, however, mice that lack a functional form of this enzyme show normal skeletal development. This enzyme has been linked directly to a disorder known as hypophosphatasia, a disorder that is characterized by hypercalcemia and includes skeletal defects. The character of this disorder can vary, however, depending on the specific mutation since this determines age of onset and severity of symptoms.
Background
Alkaline phosphatase, tissue-nonspecific isozyme (ALPL) is an enzyme encoded by the ALPL gene in humans. It is also commonly known as tissue-nonspecific alkaline phosphatase (TNAP). ALPL is a type of alkaline phosphatase found in bone, liver, kidney, and intestine. ALPL plays a crucial role in bone mineralization and is involved in the regulation of phosphate metabolism. It catalyzes the hydrolysis of phosphate esters in an alkaline environment, leading to the release of inorganic phosphate. In bone tissue, ALPL is primarily expressed by osteoblasts, where it helps in the mineralization process by generating inorganic phosphate ions, which are essential for the formation of hydroxyapatite crystals, the main component of bone mineral. Deficiencies or mutations in the ALPL gene can lead to a rare genetic disorder known as hypophosphatasia (HPP). HPP is characterized by defective bone mineralization, resulting in weak and soft bones, skeletal abnormalities, and a range of other symptoms depending on the severity of the condition.
Características del producto
category
Primary Antibodies
clonality
Polyclonal
reactivity
Human, Mouse
immunogen target
Alkaline Phosphatase, Tissue-Nonspecific Isozyme (ALPL)
host
Rabbit
isotype
IgG
conjugation
Unconjugated
form
Liquid
tested applications
ELISA, WB, IHC, IF/ICC, FCM
purification
Purified through a protein A column, followed by peptide affinity purification.
recommended dilution
WB: 1/2000, IHC-P: 1/500, IF/ICC: 1/10 - 1/50, FCM: 1/10 - 1/50. Not tested in IHC-F. Optimal dilutions/concentrations should be determined by the end user.
buffer
PBS containing 0.09% sodium azide.
size 1
80 µl
size 2
400 µl
storage
Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles.
or code
ALPL
dry ice
No
availability
Shipped within 5-10 working days.
alias
AP-TNAP,TNS-ALP
uniprot id
NCBI accession
NP_000469.3, NP_001120973.2, NP_001170991.1
note
Concentration: 0.5 mg/ml -
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