LPIN2 Antibody

• Background:

  Defects in LPIN2 are the cause of Majeed syndrome. Majeed syndrome is an autosomal recessive disorder combining features of chronic recurrent multifocal osteomyelitis, congenital dyserythropoietic anemia and inflammatory dermatosis.

• NCBI Gene ID:

  9663

• Swiss Prot:

  Q92539

• Accession Number:

  Q92539

• Host:

  Rabbit

• Reactivity:

  Human

• Immunogen:

  This LPIN2 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 262-288 amino acids from the Central region of human LPIN2.

• Clonality:

  Polyclonal

• Conjugation:

  Unconjugated

• Type:

  Primary Antibodies

• Field of Research:

  Obesity, Signal Transduction

• Purification:

  This antibody is purified through a protein A column, followed by peptide affinity purification.

• Concentration:

  Batch dependent

• Buffer:

  Supplied in PBS with 0.09% (W/V) sodium azide.

• Modification:

  None

• Shipping Conditions:

  Blue Ice

• Storage Conditions:

  Store at 4˚ C for three months and -20˚ C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.

• Calculated Molecular Weight:

  99 kDa

• Fragment:

  Rabbit Ig

• Symbol:

  LPIN2

• NCBI Official Name:

  Phosphatidate phosphatase LPIN2

• NCBI Organism:

  Homo sapiens

• Background Reference 01:

  Olsen, J.V., et.al., Cell 127 (3), 635-648 (2006)

• Background Reference 02:

  Ferguson, P.J., et.al., J. Med. Genet. 42 (7), 551-557 (2005)

• Other Product Names:

  Phosphatidate phosphatase LPIN2, Lipin-2, LPIN2, KIAA0249

• Tested Applications:

  WB, IHC-P, Flow

• Protein ID:

  2495724

• Physical Properties:

  Liquid