Manufacturer |
ProSci
|
Category |
|
Type |
Antibody Polyclonal |
Specific against |
Human |
Format |
Liquid |
Applications |
WB |
Amount |
400 ul |
Host |
Rabbit |
Item no. |
PRS-58-985-400ul |
eClass 6.1 |
32160702 |
eClass 9.0 |
32160702 |
Available |
|
Alias |
Palmitoyl-protein thioesterase 1, PPT-1, Palmitoyl-protein hydrolase 1, PPT1, PPT |
Shipping |
blue ice or RT |
By Research Area |
Obesity, Signal Transduction |
Homology |
Predicted species reactivity based on immunogen sequence: Monkey |
Immunogen |
This PPT1 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 189-217 amino acids from the Central region of human PPT1. |
Applications |
For WB starting dilution is: 1:1000 |
Predicted Molecular Weight |
34 kDa |
Purification |
This antibody is purified through a protein A column, followed by peptide affinity purification. |
Clonality |
Polyclonal |
Isotype |
Rabbit Ig |
Conjugate |
Unconjugated |
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. |
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. |
Modifications |
None |
Ncbi Official Symbol |
PPT1 |
Accession # |
P50897 |
Protein Gi # |
1709747 |
Ncbi Gene Id # |
5538 |
User Note |
Optimal dilutions for each application to be determined by the researcher. |
Ncbi Official Symbol |
PPT1 |
Ncbi Official Full Name |
Palmitoyl-protein thioesterase 1 |
Ncbi Organism |
Homo sapiens |
Swissprot # |
P50897 |
Background |
The protein encoded by this gene is a small glycoproteininvolved in the catabolism of lipid-modified proteins duringlysosomal degradation. The encoded enzyme removes thioester-linkedfatty acyl groups such as palmitate from cysteine residues. Defectsin this gene are a cause of infantile neuronal ceroidlipofuscinosis 1 (CLN1, or INCL) and neuronal ceroid lipofuscinosis4 (CLN4). Two transcript variants encoding different isoforms havebeen found for this gene. |
Background References 1 |
Ohno, K., et al. Brain Dev. 32(7):524-530(2010) |
Background References 2 |
Simonati, A., et al. Pediatr. Neurol. 40(4):271-276(2009) |
Background References 3 |
Martins-de-Souza, D., et al. Eur Arch Psychiatry Clin Neurosci 259(3):151-163(2009) |
Background References 4 |
Kousi, M., et al. Brain 132 (PT 3), 810-819 (2009) : |
1st Image Caption |
Western blot analysis in A549 cell line lysates (35ug/lane). |
2nd Image Caption |
Western blot analysis of PPT1 using rabbit polyclonal PPT1 Antibody using 293 cell lysates (2 ug/lane) either nontransfected (Lane 1) or transiently transfected (Lane 2) with the PPT1 gene. |
Note: The presented information and documents (Manual, Product Datasheet, Safety Datasheet and Certificate of Analysis) correspond to our latest update and should serve for orientational purpose only. We do not guarantee the topicality. We would kindly ask you to make a request for specific requirements, if necessary.
All products are intended for research use only (RUO). Not for human, veterinary or therapeutic use.