Lipin 1 anticorps

N° du produit ABIN7229428

Cet anticorps anti-Lipin 1 est un anticorps Lapin Polyclonal détectant Lipin 1 dans WB et ELISA. Adapté pour Humain et Souris.

Aperçu rapide pour Lipin 1 anticorps (ABIN7229428)

Antigène: Lipin 1 (LPIN1)

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Lipin 1 est non-conjugé

Application: Western Blotting (WB), ELISA

Détail du produit anti-Lipin 1 anticorps

Fonction: LPIN1 Polyclonal Antibody

Specificité: The antibody detects endogenous levels of LPIN1 protein

Purification: The antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen

Immunogène: Synthesized peptide derived from part region of human LPIN1 protein

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 (1:500-1:2000), ELISA (1:5000-1:20000).

Commentaires:

Primary Antibody

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: PBS, pH 7.4, containing 0.02 % Sodium Azide as preservative and 50 % Glycerol.

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: -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.

Détails sur Lipin 1

Antigène: Lipin 1 (LPIN1)

Autre désignation: LPIN1

Sujet: Rabbit Anti-LPIN1 Polyclonal Antibody,Phosphatidate phosphatase LPIN1, Lipin-1,LPIN1 encodes a magnesium-ion-dependent phosphatidic acid phosphohydrolase enzyme that catalyzes the penultimate step in triglyceride synthesis including the dephosphorylation of phosphatidic acid to yield diacylglycerol. Expression of this gene is required for adipocyte differentiation and it also functions as a nuclear transcriptional coactivator with some peroxisome proliferator-activated receptors to modulate expression of other genes involved in lipid metabolism. Mutations in this gene are associated with metabolic syndrome, type 2 diabetes, acute recurrent rhabdomyolysis, and autosomal recessive acute recurrent myoglobinuria (ARARM). This gene is also a candidate for several human lipodystrophy syndromes.,LPIN1

Poids moléculaire: observerd band 97kDa

ID gène: 23175

UniProt: Q14693

Pathways: Monocarboxylic Acid Catabolic Process