LPIN2 Antibody
Product Specifications
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.
Product Datasheet
https://www.prosci-inc.com/?datasheet_sku=63-529
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
Curated Selection
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