PIPA585126

LPL Polyclonal Antibody, Invitrogen™

Manufacturer: Thermo Scientific

Select a Size

Pack Size SKU Availability Price
Each of 1 PIPA585126-Each-of-1 In Stock ₹ 46,146.50

PIPA585126 - Each of 1

₹ 46,146.50

In Stock

Quantity

1

Base Price: ₹ 46,146.50

GST (18%): ₹ 8,306.37

Total Price: ₹ 54,452.87

Antigen

LPL

Classification

Polyclonal

Conjugate

Unconjugated

Gene

LPL

Gene Alias

adipose lipoprotein lipase, alpha lipase, HDLCQ11, I79_006077, LIPD, lipoprotein lipase, lipoprotein lipase (EC 3.1.1.34), lipoprotein lipase precursor, lipoprotein lipase preprotein, Lipoprotein lipase-like protein, LPL, O 1-4-5, phospholipase A1, triacylglycerol lipase

Host Species

Rabbit

Purification Method

Antigen affinity chromatography

Regulatory Status

RUO

Gene ID (Entrez)

16956, 396219, 4023

Content And Storage

Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.

Form

Liquid

Applications

Immunocytochemistry, Western Blot, Western Blot

Concentration

0.11 mg/mL

Formulation

PBS with 1% BSA, 20% glycerol and 0.025% ProClin 300, pH 7

Gene Accession No.

P06858, P11152, P11602

Gene Symbols

LPL

Immunogen

Recombinant protein encompassing a sequence within the center region of human LPL.

Quantity

100 μL

Primary or Secondary

Primary

Target Species

Chicken, Human, Mouse

Product Type

Antibody

Isotype

IgG

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Description

  • Keep as concentrated solution
  • Predicted reactivity: Mouse (90%), Rat (90%), Cat (94%), Pig (93%), Rabbit (92%), Sheep (91%), Bovine (91%), Guinea pig (86%)
  • Positive Control: Molt-4, NIH-3T3
  • Store product as a concentrated solution
  • Centrifuge briefly prior to opening the vial
  • LPL encodes lipoprotein lipase, which is expressed in heart, muscle, and adipose tissue
  • LPL functions as a homodimer, and has the dual functions of triglyceride hydrolase and ligand/bridging factor for receptor-mediated lipoprotein uptake
  • Severe mutations that cause LPL deficiency result in type I hyperlipoproteinemia, while less extreme mutations in LPL are linked to many disorders of lipoprotein metabolism.