Lipoprotein Lipase antibody (C-Term)
-
- Target See all Lipoprotein Lipase (LPL) Antibodies
- Lipoprotein Lipase (LPL)
-
Binding Specificity
- C-Term
-
Reactivity
- Human, Rat, Cow, Pig, Goat, Horse, Dog, Rabbit, Sheep
-
Host
- Rabbit
-
Clonality
- Polyclonal
-
Conjugate
- This Lipoprotein Lipase antibody is un-conjugated
-
Application
- Western Blotting (WB), Immunohistochemistry (IHC)
- Sequence
- LGYEINKVRA KRSSKMYLKT RSQMPYKVFH YQVKIHFSGT ESETHTNQAF
- Predicted Reactivity
- Cow: 86%, Dog: 79%, Goat: 86%, Horse: 86%, Human: 100%, Pig: 92%, Rabbit: 86%, Rat: 86%, Sheep: 86%
- Characteristics
- This is a rabbit polyclonal antibody against LPL. It was validated on Western Blot.
- Purification
- Affinity Purified
- Immunogen
- The immunogen is a synthetic peptide directed towards the C terminal region of human LPL
- Top Product
- Discover our top product LPL Primary Antibody
-
-
- Application Notes
- Optimal working dilutions should be determined experimentally by the investigator.
- Comment
-
Antigen size: 475 AA
- Restrictions
- For Research Use only
-
- Format
- Liquid
- Concentration
- Lot specific
- Buffer
- Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.
- Preservative
- Sodium azide
- Precaution of Use
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Handling Advice
- Avoid repeated freeze-thaw cycles.
- Storage
- -20 °C
- Storage Comment
- For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
-
- Target
- Lipoprotein Lipase (LPL)
- Alternative Name
- LPL (LPL Products)
- Synonyms
- HDLCQ11 antibody, LIPD antibody, fb62e04 antibody, fc49b03 antibody, wu:fb62e04 antibody, wu:fc49b03 antibody, LPL antibody, lipd antibody, hdlcq11 antibody, lpl antibody, LOC100223817 antibody, lipoprotein lipase antibody, LPL antibody, Lpl antibody, lpl antibody
- 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.
Alias Symbols: HDLCQ11, LIPD
Protein Interaction Partner: LMF1, LPL, CALR, CCND1, APP, CUL3, UBC, PLK1, LUC7L2, KIAA1377, COPS6, ASCC2, RPL18A, UBE2Z, APOC2, LRP2, VLDLR, PTPN4, CETP, LRP1, EMD,
Protein Size: 475 - Molecular Weight
- 50 kDa
- Gene ID
- 4023
- NCBI Accession
- NM_000237, NP_000228
- UniProt
- P06858
- Pathways
- Lipid Metabolism
-