Lipin 1 anticorps
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- Antigène Voir toutes Lipin 1 (LPIN1) Anticorps
- Lipin 1 (LPIN1)
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Reactivité
- Humain, Rat, Souris
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Hôte
- Lapin
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Clonalité
- Polyclonal
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Conjugué
- Cet anticorp Lipin 1 est non-conjugé
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Application
- Western Blotting (WB), ELISA
- Purification
- Antibody is purified by peptide affinity chromatography method.
- Immunogène
- Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human LPIN1.
- Top Product
- Discover our top product LPIN1 Anticorps primaire
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- Indications d'application
- LPIN1 antibody can be used for detection of LPIN1 by ELISA at 1:12500. LPIN1 antibody can be used for detection of LPIN1 by western blot at 1 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.
- Restrictions
- For Research Use only
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- Format
- Lyophilized
- Reconstitution
- Add 50 ?L of distilled water. Final antibody concentration is 1 mg/mL.
- Concentration
- 1 mg/mL
- Buffer
- Antibody is lyophilized in PBS buffer with 2 % sucrose.
- Conseil sur la manipulation
- As with any antibody avoid repeat freeze-thaw cycles.
- Stock
- 4 °C/-20 °C
- Stockage commentaire
- For short periods of storage (days) store at 4 °C. For longer periods of storage, store LPIN1 antibody at -20 °C.
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- Antigène
- Lipin 1 (LPIN1)
- Autre désignation
- LPIN1 (LPIN1 Produits)
- Synonymes
- anticorps LPIN1, anticorps pap1, anticorps PAP1, anticorps 4631420P06, anticorps Kiaa0188, anticorps Lipin1, anticorps fld, anticorps mKIAA0188, anticorps zgc:194552, anticorps zgc:194558, anticorps lipin1, anticorps lipin 1, anticorps phosphatidate phosphatase LPIN1, anticorps LPIN1, anticorps lpin1, anticorps LOC100539289, anticorps Lpin1
- Sujet
- This gene represents a candidate gene for human lipodystrophy, characterized by loss of body fat, fatty liver, hypertriglyceridemia, and insulin resistance. Mouse studies suggest that LPIN1 functions during normal adipose tissue development and may also play a role in human triglyceride metabolism. This gene represents a candidate gene for human lipodystrophy, characterized by loss of body fat, fatty liver, hypertriglyceridemia, and insulin resistance. Mouse studies suggest that this gene functions during normal adipose tissue development and may also play a role in human triglyceride metabolism. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.
- Poids moléculaire
- 98 kDa
- ID gène
- 23175
- NCBI Accession
- NP_663731
- UniProt
- Q14693
- Pathways
- Monocarboxylic Acid Catabolic Process
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