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Lipin 2 (LPIN2) Antibody
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Catalogue No: abx034008
Price:
US$290.00
(Size: 80 µl)
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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.
Research Articles on Lipin 2 (LPIN2)
| Target | Lipin 2 (LPIN2) |
| Clonality | Polyclonal |
| Reactivity | Human |
| Tested Applications | ELISA, WB, IHC, FCM |
| Host | Rabbit |
| Recommended dilutions | WB: 1/1000, IHC-P: 1/50 - 1/100, FCM: 1/10 - 1/50. Not tested in IHC-F. Optimal dilutions/concentrations should be determined by the end user. |
| Conjugation | Unconjugated |
| Immunogen | KLH-conjugated synthetic peptide between 262-288 amino acids from the Central region of human LPIN2. |
| Isotype | IgG |
| Form | Liquid |
| Purification | Purified through a protein A column, followed by peptide affinity purification. |
| Storage | Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles. |
| UniProt Primary AC | Q92539 (UniProt, ExPASy) |
| UniProt Secondary AC | A7MD25, D3DUH3 |
| UniProt Entry Name | LPIN2_HUMAN |
| Gene Symbol | LPIN2 |
| KEGG | hsa:9663 |
| String | 9606.ENSP00000261596 |
| Molecular Weight | Calculated MW: 99.4 kDa |
| Buffer | PBS containing 0.09% sodium azide. |
| Availability | Shipped within 5-10 working days. |
| Note | This product is for research use only. |
