LPIN2 Antibody (Center) Blocking Peptide
€363.00
In stock
SKU
AC-BP8583c
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.
Other Names:
Phosphatidate phosphatase LPIN2, Lipin-2, LPIN2, KIAA0249
Target/Specificity:
The synthetic peptide sequence used to generate the antibody AP8583c was selected from the Center region of human LPIN2. A 10 to 100 fold molar excess to antibody is recommended. Precise conditions should be optimized for a particular assay.
Gene Name: LPIN2 (HGNC:14450)
Gene ID: 9663
Primary Accession: Q92539
Format: Peptides are lyophilized in a solid powder format. Peptides can be reconstituted in solution using the appropriate buffer as needed.
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.
Other Names:
Phosphatidate phosphatase LPIN2, Lipin-2, LPIN2, KIAA0249
Target/Specificity:
The synthetic peptide sequence used to generate the antibody AP8583c was selected from the Center region of human LPIN2. A 10 to 100 fold molar excess to antibody is recommended. Precise conditions should be optimized for a particular assay.
Gene Name: LPIN2 (HGNC:14450)
Gene ID: 9663
Primary Accession: Q92539
Format: Peptides are lyophilized in a solid powder format. Peptides can be reconstituted in solution using the appropriate buffer as needed.
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