LSM2 anticorps (AA 40-120)

N° du produit ABIN7229464

Cet anticorps anti-LSM2 Polyclonal Lapin (ABIN7229464) détecte spécifiquement LSM2 dans WB et ELISA. L’anticorps est réactif avec des échantillons de Humain et Souris.

Aperçu rapide pour LSM2 anticorps (AA 40-120) (ABIN7229464)

Antigène: LSM2 (LSM2 Homolog, U6 Small Nuclear RNA Associated (LSM2))

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp LSM2 est non-conjugé

Application: Western Blotting (WB), ELISA

Détail du produit anti-LSM2 anticorps

Épitope: AA 40-120

Fonction: Rabbit Anti-LSM2 Polyclonal Antibody

Specificité: The antibody detects endogenous levels of LSM2 protein

Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Immunogène: Synthesized peptide derived from part region of human LSM2 protein at AA range: 40-120

Isotype: IgG

Information d'application

Indications d'application: Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB 1:500-2000,ELISA 1:5000-20000

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: PBS, 50 % glycerol, 0.05 % Proclin 300, 0.05 %BSA

Agent conservateur: ProClin

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

Stock: -20 °C

Stockage commentaire: Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.

Date de péremption: 12 months

Détails sur LSM2

Antigène: LSM2 (LSM2 Homolog, U6 Small Nuclear RNA Associated (LSM2))

Autre désignation: LSM2

Sujet: U6 snRNA-associated Sm-like protein LSm2, Protein G7b, Small nuclear ribonuclear protein D homolog, snRNP core Sm-like protein Sm-x5LSM2 (LSM2 Homolog, U6 Small Nuclear RNA And MRNA Degradation Associated) is a Protein Coding gene. Diseases associated with LSM2 include Spinal Muscular Atrophy and Rheumatic Disease. Among its related pathways are Translational Control and mRNA Splicing - Major Pathway. LSM2 encodes a member of the LSm family of RNA-binding proteins. LSm proteins form stable heteromers that bind specifically to the 3'-terminal oligo(U) tract of U6 snRNA and may play a role in pre-mRNA splicing by mediating U4/U6 snRNP formation. Pseudogenes of this gene are located on the short arm of chromosomes 6 and 19.

Poids moléculaire: 10kD

ID gène: 57819

UniProt: Q9Y333

Pathways: Ribonucleoprotein Complex Subunit Organization