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Lipoprotein Lipase antibody (AA 124-475)

This anti-Lipoprotein Lipase antibody is a Rabbit Polyclonal antibody detecting Lipoprotein Lipase in WB. Suitable for Human.
Catalog No. ABIN7268286

Quick Overview for Lipoprotein Lipase antibody (AA 124-475) (ABIN7268286)

Target

See all Lipoprotein Lipase (LPL) Antibodies
Lipoprotein Lipase (LPL)

Reactivity

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Human

Host

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Rabbit

Clonality

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Polyclonal

Conjugate

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This Lipoprotein Lipase antibody is un-conjugated

Application

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Western Blotting (WB)
  • Binding Specificity

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    AA 124-475

    Purpose

    Lipoprotein lipase (LPL) Rabbit pAb

    Sequence

    SAGYTKLVGQ DVARFINWME EEFNYPLDNV HLLGYSLGAH AAGIAGSLTN KKVNRITGLD PAGPNFEYAE APSRLSPDDA DFVDVLHTFT RGSPGRSIGI QKPVGHVDIY PNGGTFQPGC NIGEAIRVIA ERGLGDVDQL VKCSHERSIH LFIDSLLNEE NPSKAYRCSS KEAFEKGLCL SCRKNRCNNL GYEINKVRAK RSSKMYLKTR SQMPYKVFHY QVKIHFSGTE SETHTNQAFE ISLYGTVAES ENIPFTLPEV STNKTYSFLI YTEVDIGELL MLKLKWKSDS YFSWSDWWSS PGFAIQKIRV KAGETQKKVI FCSREKVSHL QKGKAPAVFV KCHDKSLNKK SG

    Cross-Reactivity

    Human, Mouse, Rat

    Characteristics

    Polyclonal Antibodies

    Purification

    Affinity purification

    Immunogen

    Recombinant fusion protein containing a sequence corresponding to amino acids 124-475 of human Lipoprotein lipase (Lipoprotein lipase (LPL)) (NP_000228.1).

    Isotype

    IgG
  • Application Notes

    WB,1:500 - 1:2000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

    Preservative

    Sodium azide

    Precaution of Use

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Storage

    -20 °C

    Storage Comment

    Store at -20°C. Avoid freeze / thaw cycles.
  • Target

    Lipoprotein Lipase (LPL)

    Alternative Name

    LPL

    Background

    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.,LPL,HDLCQ11,LIPD,Cancer,Signal Transduction,Endocrine & Metabolism,Lipid Metabolism,Lipases,Endocrine and metabolic diseases,Obesity,Neuroscience,Neurodegenerative Diseases,Stem Cells,Mesenchymal Stem Cells,Cardiovascular,Lipids,LPL

    Molecular Weight

    53kDa

    Gene ID

    4023

    UniProt

    P06858

    Pathways

    Lipid Metabolism
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