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Invitrogen™ LPIN3 Polyclonal Antibody
GREENER_CHOICE

Goat Polyclonal Antibody

Supplier:  Invitrogen™ PA518590

Catalog No. PIPA518590


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Description

Description

This antibody is tested in Peptide ELISA: antibody detection limit dilution 64,000.

Humans lipodystrophy is characterized by loss of body fat, fatty liver, hypertriglyceridemia, and insulin resistance. Mice carrying mutations in the fatty liver dystrophy gene have similar phenotypes. Through positional cloning, the mouse gene responsible for fatty liver dystrophy was isolated and designated Lpin1. The nuclear protein encoded by Lpin1 was named lipin. Lpin1 mRNA was expressed at high levels in adipose tissue and was induced during differentiation of preadipocytes. These results indicated that lipin is required for normal adipose tissue development and provided a candidate gene for human lipodystrophy. Through database searches, mouse and human EST and genomic sequences with similarities to Lpin1 were identified. These included two related mouse genes and three human homologs. Human LPIN1 gene has been mapped to 2p25.; linkages of fat mass and serum leptin levels to this same region have been noted. Human LPIN2 and LPIN3 mapped to chromosomes 18p11 and 20q11-q12, respectively. The mouse genes encoding Lpin1, Lpin2, and Lpin3 mapped to chromosome 12, 17, and 2, respectively.
TRUSTED_SUSTAINABILITY
Specifications

Specifications

LPIN3
Polyclonal
Unconjugated
LPIN3
9130206L11Rik; AA438110; AV236139; dJ450M14.2; dJ450M14.3; dJ620E11.2; lipin 3; lipin 3-like; lipin-3; Lipin-3-like; LIPN3L; Lpin3; mKIAA4023; Phosphatidate phosphatase LPIN3; RP4-620E11.3; SMP2
Goat
Ammonium sulfate precipitation
RUO
64900
-20°C, Avoid Freeze/Thaw Cycles
Liquid
Immunohistochemistry (Paraffin), Western Blot
0.5 mg/mL
TBS with 0.5% BSA and 0.02% sodium azide; pH 7.3
Q9BQK8
LPIN3
Synthetic peptide sequence (KPKQKEDAVATD) corresponding to the internal amino acids of LPIN3 (aa 149-161).
100 μg
Primary
Human
Antibody
IgG
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