Perilipin-1 Antibodies

AND PLIN1 ELISA kits, Perilipin-1 Proteins

Many biological assays use antibodies to detect Perilipin-1, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with Perilipin-1 in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop Perilipin-1 antibodies...

We validate the specificity of these antibodies to Perilipin-1 by testing them on tissues known to express PLIN1 positively and negatively. Browse below to find the PLIN1 antibody that suites your experiment. We have 5 of these antibodies and many publications and validation images.

If you cannot find antibodies that fit your needs, contact us for making custom antibodies. We have a full suite of custom antibody services covering from research to diagnostic and therapeutic applications.

Previous: CBLIF Next: FXYD3

PLIN1 Infographic by Boster Bio

All PLIN1 Products

Filter by Application:

Product

Figures

Specificity

Applications

Price

Anti-Perilipin A/PLIN1 Antibody Picoband®

3 Citations 4 Q&As

Western blot analysis of Perilipin A using anti-Perilipin A antibody (A03918-1)

Antioxidants preserve ADSC cell stemness and multidirectional differentiation potential during long-term in vitro expansion

Human, Mouse, Rat

$370
Cat # A03918-1
100 μg/vial

Anti-Perilipin A PLIN1 Rabbit Monoclonal Antibody

1 Citations 15 Q&As

All lanes use the Antibody at 1:3K dilution for 1 hour at room temperature

Western blot analysis of Perilipin A expression in human fetal liver lysate

Western blot analysis of PLIN1 using anti-PLIN1 antibody (M03918)

Human, Mouse

IF, ICC, WB

$370
Cat # M03918
100 μl

Perilipin-1 (PLIN1) (NM_002666) Human Over-expression Lysate

Perilipin-1 (PLIN1) Human Over-expression Lysates NM_001145311

Human

$628
Cat # LS005346
20 µg, 100 µg

Anti-Perilipin-1 Rabbit Monoclonal Antibody

Human adipose was stained with anti-Perilipin-1 rabbit antibody

Mouse adipose was stained with anti-Perilipin-1 rabbit antibody

Rat adipose was stained with anti-Perilipin-1 rabbit antibody

Human, Mouse, Rat

ELISA, IP, IF, IHC, WB

$146
Cat # M03918-1
20μL, 40μL, 100μL, 200μL

Anti-Phospho-PLIN1 (S522) Antibody

Human, Mouse, Rat

IHC

$370
Cat # P03918
100 μl/vial

PLIN1 Overview

Facts about Perilipin-1.

PLIN1 3D structure. Source: alphafold

Perilipin-1 (PLIN1)

Modulator of adipocyte lipid metabolism. Coats lipid storage droplets to protect them from breakdown by hormone- sensitive lipase (HSL).

Its absence may result in leanness. Plays a role in unilocular lipid droplet formation by activating CIDEC.

Gene Information

Human
Gene Name:	PLIN1
Uniprot:	O60240
Entrez:	5346

Family

Belongs to:

perilipin family

Alternative Names

PERI; perilipin 1; Perilipin; perilipin-1; PLIN; PLIN1; PLINLipid droplet-associated protein

Molecular Weight

Mass (kDA):
55.99 kDA

Genomic Context


Human

Location:	15q26.1
Sequence:	15; NC_000015.10 (89664365..89679367, complement)

Tissue Specificity

Adipocytes.

Subcellular Localizations

Endoplasmic reticulum. Lipid droplet. Lipid droplet surface-associated.

Diseases

Obesity
Insulin Resistance
Acquired Partial Lipodystrophy
Dysequilibrium Syndrome
Lipodystrophy
Diabetes Mellitus
Mutation, Out-of-frame
Metabolic Syndrome X
Steatohepatitis
Steatosis
Familial Partial Lipodystrophy
Liver Diseases
Dyslipidemias

Familial Generalized Lipodystrophy
Coronary Artery Disease
Inflammatory Response
Fibrosis
Cardiovascular Diseases
Osteoporosis
Bone Diseases

Pathways

Localization
Lipid Oxidation
Lipid Homeostasis
Aging
Lipid Storage
Fatty Acid Oxidation

Inflammatory Response

PTMs

Phosphorylation

Oxidation

Research Areas

Diabetes Research
Lipid and Metabolism
Lipid Droplets

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/PLIN1

References

PMID: 9521880 by Nishiu J., et al. Isolation and chromosomal mapping of the human homolog of perilipin (PLIN), a rat adipose tissue-specific gene, by differential display method.

PMID: 21345103 by Gandotra S., et al. Perilipin deficiency and autosomal dominant partial lipodystrophy.