Recombinant SPTA1 anticorps (AA 356-475)

N° du produit ABIN6654217

L’anticorps anti-SPTA1 Monoclonal Souris est utilisé pour la détection de SPTA1 dans des échantillons de Humain. Il a été validé pour IHC (p) et WB.

Aperçu rapide pour Recombinant SPTA1 anticorps (AA 356-475) (ABIN6654217)

Antigène: SPTA1 (Spectrin alpha Chain, Erythrocytic 1 (SPTA1))

Type d'anticorp: Recombinant Antibody

Reactivité: Humain

Hôte: Souris

Clonalité: Monoclonal

Conjugué: Cet anticorp SPTA1 est non-conjugé

Application: Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Western Blotting (WB)

Classe de qualité: Carrier-free

Clone: SCNA-1R

Détail du produit anti-SPTA1 anticorps

Épitope: AA 356-475

Fonction: Recombinant SPTA1 Antibody / Spectrin alpha 1 (azide and preservative free)

Purification: Protein G affinity chromatography

Immunogène: A portion of amino acids 356-475 from the human protein was used as the immunogen for the recombinant SPTA1 antibody.

Isotype: IgG1, kappa

Information d'application

Indications d'application: The stated application concentrations are suggested starting points. Titration of the recombinant SPTA1 antibody may be required due to differences in protocols and secondary/substrate sensitivity.

1. The prediluted format is supplied in a dropper bottle and is optimized for use in IHC. After epitope retrieval step (if required), drip mAb solution onto the tissue section and incubate at RT for 30 min.

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: 1 mg/mL in 1X PBS, BSA free, sodium azide free

Agent conservateur: Azide free

Stock: 4 °C,-20 °C

Stockage commentaire: Store the recombinant SPTA1 antibody at 2-8oC (with azide) or aliquot and store at -20oC or colder (without azide).

Détails sur SPTA1

Antigène: SPTA1 (Spectrin alpha Chain, Erythrocytic 1 (SPTA1))

Autre désignation: SPTA1 / Spectrin alpha 1

Sujet: This gene encodes a member of a family of molecular scaffold proteins that link the plasma membrane to the actin cytoskeleton and functions in the determination of cell shape, arrangement of transmembrane proteins, and organization of organelles. The encoded protein is primarily composed of 22 spectrin repeats which are involved in dimer formation. It forms a component of the erythrocyte plasma membrane. Mutations in this gene result in a variety of hereditary red blood cell disorders, including elliptocytosis-2, pyropoikilocytosis, and spherocytosis, type 3. [RefSeq]

UniProt: P02549