ATP2C1 anticorps (C-Term)

N° du produit ABIN1537638

Détail du produit anti-ATP2C1 anticorps

Antigène: ATP2C1 (ATPase, Ca++ Transporting, Type 2C, Member 1 (ATP2C1))

Épitope: AA 882-909, C-Term

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp ATP2C1 est non-conjugé

Application: Western Blotting (WB)

Purification: This antibody is purified through a protein A column, followed by peptide affinity purification.

Immunogène: This ATP2C1 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 882-909 amino acids from the C-terminal region of human ATP2C1.

Clone: RB36281

Isotype: Ig Fraction

Information d'application

Indications d'application: WB: 1:1000

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: 4 °C,-20 °C

Stockage commentaire: ATP2C1 Antibody (C-term) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, keep at -20 °C.

Date de péremption: 6 months

Détails sur ATP2C1

Antigène: ATP2C1 (ATPase, Ca++ Transporting, Type 2C, Member 1 (ATP2C1))

Autre désignation: ATP2C1 (ATP2C1 Produits)

Synonymes: anticorps ATP2C1, anticorps ATP2C1A, anticorps BCPM, anticorps HHD, anticorps PMR1, anticorps SPCA1, anticorps hSPCA1, anticorps Spca1, anticorps si:dkey-11p23.6, anticorps SPCA, anticorps 1700121J11Rik, anticorps AW061228, anticorps D930003G21Rik, anticorps pmr1, anticorps ATPase secretory pathway Ca2+ transporting 1, anticorps ATPase, Ca++ transporting, type 2C, member 1, anticorps ATPase, Ca++-sequestering, anticorps ATP2C1, anticorps atp2c1, anticorps Atp2c1

Sujet: The protein encoded by this gene belongs to the family of P-type cation transport ATPases. This magnesium-dependent enzyme catalyzes the hydrolysis of ATP coupled with the transport of the calcium. Defects in this gene cause Hailey-Hailey disease, an autosomal dominant disorder. Alternatively spliced transcript variants encoding different isoforms have been identified.

Poids moléculaire: 100577

ID gène: 27032

NCBI Accession: NP_001001485, NP_001001486, NP_001001487, NP_001186108, NP_001186109, NP_001186110, NP_001186111, NP_001186112, NP_001186113, NP_001186114, NP_055197

UniProt: P98194

Pathways: Transition Metal Ion Homeostasis, Ribonucleoside Biosynthetic Process