Description
PEX10 (CT) Antibody | 9671 | Gentaur UK, US & Europe Distribution
Product Type: Primary Antibodies
Category: Primary Antibodies, Polyclonal Antibodies, Signal Transduction Antibodies
Research Area: Signal Transduction
Type: Polyclonal
Host Species: Rabbit
Reactivity Species: Human, Mouse, Rat
Homology: Predicted species reactivity based on immunogen sequence: monkey (100%), horse (100%), gorilla (100%), chimpanzee (100%)
Immunology: Anti-PEX10 antibody (9671) was raised against a peptide corresponding to 10 amino acids near the carboxyl terminus of human PEX10.
The immunogen is located within last 50 amino acids of PEX10.
Tested Application: E, WB, IF
Application Note: WB: 4 μg/mL; IF: 20 μg/mL.
Antibody validated: Western Blot in human, mouse and rat samples; Immunofluorescence in human, mouse and rat samples. All other applications and species not yet tested.
Positive Control 1: Cat. No. 1203 – A549 Cell Lysate
Positive Control 2: Cat. No. 17-003 – A549 Cell Slide
Predicted Molecular Weight: Predicted: 37kD
Observed: 37 kD
Isoform: Human PEX10 has 2 isoforms, including isoform 1 (326aa, 37.1kD) and isoform 2 (346aa, 39.2kD) . Mouse PEX10 has 1 isoform (324aa, 37.2kD) . 9671 can detect PEX10 in human and mouse.
Purification: PEX10 Antibody is affinity chromatography purified via peptide column.
Clonality: Polyclonal
Clone: N/A
Isotype: IgG
Conjugate: Unconjugated
Physical State: Liquid
Buffer: PEX10 Antibody is supplied in PBS containing 0.02% sodium azide.
Concentration: 1 mg/mL
Storage: PEX10 antibody can be stored 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.
Additional Names: PEX10 Antibody: Peroxin-10, Peroxisomal biogenesis factor 10, Peroxisome assembly protein 10, RING finger protein 69, RNF69
Protein Accession: O60683
User Note: Optimal dilutions for each application to be determined by the researcher.
Background: PEX10 is implicated in the biogenesis of peroxisomes. Mutations in this gene result in phenotypes within the Zellweger spectrum of peroxisomal biogenesis disorders, ranging from neonatal adrenoleukodystrophy to Zellweger syndrome.
Loading Controls: N/A
Source: N/A
Purity: N/A
CAS: N/A
Shipping Condition: N/A