Alkaline Phosphatase, Tissue-Nonspecific Isozyme (ALPL) Antibody

Este producto es parte de ALPL - Alkaline phosphatase tissue-nonspecific isozyme
Alkaline Phosphatase, Tissue-Nonspecific Isozyme (ALPL) Antibody

Pida mas información

935106861

info@markelab.com

Precio

292.5€ (80 µl)

Antibody anti-ALPL

proveedor

Abbexa

reference

abx028274

Tested Applications

ELISA, WB, IHC, IF/ICC, FCM

reactivity

Human, Mouse

status

RUO

clonality

Polyclonal

Descripción

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


NCBI accession

NP_000469.3, NP_001120973.2, NP_001170991.1


note

Concentration: 0.5 mg/ml -


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