ALPL anticorps

N° du produit ABIN6297134

L’anticorps Souris Monoclonal anti-ALPL a été validé pour IHC, FACS et IF. Il convient pour détecter ALPL dans des échantillons de Humain et Boeuf (Vache).

Aperçu rapide pour ALPL anticorps (ABIN6297134)

Antigène: ALPL (Alkaline Phosphatase, Liver/bone/kidney (ALPL))

Reactivité: Humain, Boeuf (Vache)

Hôte: Souris

Clonalité: Monoclonal

Conjugué: Cet anticorp ALPL est non-conjugé

Application: Immunohistochemistry (IHC), Flow Cytometry (FACS), Immunofluorescence (IF)

Détail du produit anti-ALPL anticorps

Fonction: Mouse anti-Human/Cow Alkaline Phosphatase Antibody (tissue-nonspecific) [Sodium Azide Free]

Specificité: Cell surface, cytoplasmic, secreted

Purification: Recombinant human ALPL protein was used as the immunogen for the Alkaline Phosphatase antibody.

Immunogène: Recombinant human ALPL protein was used as the immunogen for the Alkaline Phosphatase antibody.

Information d'application

Indications d'application: Flow Cytometry: 0.5-1 μg/million cells in 0.1ml
Immunofluorescence: 0.5-1 μg/mL
Immunohistochemistry (FFPE): 1-2 μg/mL for 30 min at RT
Prediluted format: incubate for 30 min at RT (1)

Restrictions: For Research Use only

Stockage

Buffer: In 1X PBS, BSA free, sodium azide free

Agent conservateur: Azide free

Stock: 4 °C,-20 °C

Stockage commentaire: 2-8°C. The azide-free format should be aliquoted and stored at -20°C or colder.

Détails sur ALPL

Antigène: ALPL (Alkaline Phosphatase, Liver/bone/kidney (ALPL))

Autre désignation: Alkaline phosphatase, tissue-nonspecific isozyme

Sujet:

Target Description: There are at least four distinct but related alkaline phosphatases: intestinal, placental, placental-like, and liver/bone/kidney (tissue non-specific). The first three are located together on chromosome 2, while the tissue non-specific form is located on chromosome 1. The product of this gene 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 hypo-phosphatasia, 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. Alternatively spliced transcript variants, which encode the same protein, have been identified for this gene.

Gene Symbol: ALPL

ID gène: 249

UniProt: P05186