Alkaline Phosphatase, Tissue-Nonspecific Isozyme (ALPL) Antibody (APC)

Este producto es parte de ALPL - Alkaline phosphatase tissue-nonspecific isozyme
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481€ (0.1 mg)

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935106861
info@markelab.com
name
Alkaline Phosphatase, Tissue-Nonspecific Isozyme (ALPL) Antibody (APC)
category
Primary Antibodies
provider
Abbexa
reference
abx140901
tested applications
FCM

Description

Alkaline Phosphatase, Tissue-Nonspecific Isozyme (ALPL) Antibody (APC) is a Mouse Monoclonal against Alkaline Phosphatase, Tissue-Nonspecific Isozyme (ALPL).

Documents del producto

Instrucciones
Data sheet
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Product specifications

Category
Primary Antibodies
Immunogen Target
Alkaline Phosphatase, Tissue-Nonspecific Isozyme (ALPL)
Host
Mouse
Reactivity
Human, Pig, Goat, Sheep, Monkey, Dog
Clonality
Monoclonal
Conjugation
APC
Isotype
IgG1
Clone ID
G860
Size 1
0.1 mg
Tested Applications
FCM
Buffer
Stabilizing PBS solution containing 15 mM sodium azide.
Availability
Shipped within 5-12 working days.
Storage
Store in the dark at 2-8°C. Avoid exposure to light. Do not freeze.
Dry Ice
No
UniProt ID
P05186
Gene ID
249
Alias
AP-TNAP,TNS-ALP
Background
Antibody anti-ALPL
Status
RUO
Note
Concentration: 0.1 mg/ml - 

Descripción

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.

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