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Western blot analysis of LPIN2 Antibody in K562 cell line lysates (35ug/lane)(2ug/ml)
Formalin-fixed and paraffin-embedded human hepatocarcinoma with LPIN2 Antibody , which was peroxidase-conjugated to the secondary antibody, followed by DAB staining.
Flow cytometric analysis of K562 cells using LPIN2 Antibody (bottom histogram) compared to a negative control cell (top histogram). FITC-conjugated goat-anti-rabbit secondary antibodies were used for the analysis.
Western blot analysis of LPIN2 Antibody in K562 cell line lysates (35ug/lane)(2ug/ml)

LPIN2 Antibody

CATALOG NUMBER: 63-529

Clonality:
Polyclonal
Tested Applications:
Flow, IHC-P, WB
Host Species:
Rabbit
Species Reactivity:
Human
Conjugate:
Unconjugated
Specifications
Host Species:
Rabbit
Species 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.
Conjugate:
Unconjugated
Tested Applications:
Flow, IHC-P, WB
Application Note:
For WB starting dilution is: 1:1000
For IHC-P starting dilution is: 1:50~100
For FACS starting dilution is: 1:10~50
Predicted Molecular Weight:
99 kDa
Purification:
This antibody is purified through a protein A column, followed by peptide affinity purification.
Clonality:
Polyclonal
Isotype:
Rabbit Ig
Physical State:
Liquid
Buffer:
Supplied in PBS with 0.09% (W/V) sodium azide.
Concentration:
batch dependent
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.
Ncbi Official Symbol:
LPIN2
Additional Names:
Phosphatidate phosphatase LPIN2, Lipin-2, LPIN2, KIAA0249
Protein Accession Number:
Q92539
Protein Gi Number:
2495724
Ncbi Gene Id Number:
9663
User Note:
Optimal dilutions for each application to be determined by the researcher.
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.
Background Reference 1:
Olsen,J.V., et.al., Cell 127 (3), 635-648 (2006)
Background Reference 2:
Ferguson,P.J., et.al., J. Med. Genet. 42 (7), 551-557 (2005)

FOR RESEARCH USE ONLY

For additional information, visit ProSci’s Terms & Conditions Page.

Disclaimer:
Optimal dilutions/concentrations should be determined by the end user. The information provided is a guideline for product use. This product is for research use only.

CATALOG NUMBER:

63-529

List Size:
400 ul

List Price:

$495.00

Datasheet
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