
Figure 1. Western blot analysis of KIM1 using anti-KIM1 antibody (PA1632). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 50ug of sample under reducing conditions. Lane 1: rat kidney tissue lysates, Lane 2: rat testis tissue lysates, Lane 3: rat heart tissue lysates. After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-KIM1 antigen affinity purified polyclonal antibody (Catalog # PA1632) at 0.5 microg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:10000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for KIM1 at approximately 50KD. The expected band size for KIM1 is at 39KD.
Anti-TIM 1/HAVCR1 Antibody Picoband(r)

PA1632-DYLIGHT594
ApplicationsWestern Blot, ImmunoHistoChemistry
Product group Antibodies
ReactivityRat
TargetHavcr1
Overview
- SupplierBoster Bio
- Product NameAnti-TIM 1/HAVCR1 Antibody Picoband(r)
- Delivery Days Customer9
- Antibody SpecificityNo cross reactivity with other proteins.
- Application Supplier NoteTested Species: In-house tested species with positive results. Predicted Species: Species predicted to be fit for the product based on sequence similarities. By Heat: Boiling the paraffin sections in 10mM citrate buffer, pH6.0, for 20mins is required for the staining of formalin/paraffin sections. Other applications have not been tested. Optimal dilutions should be determined by end users.
- ApplicationsWestern Blot, ImmunoHistoChemistry
- CertificationResearch Use Only
- ClonalityPolyclonal
- Concentration500 ug/ml
- ConjugateOther Conjugate
- Gene ID286934
- Target nameHavcr1
- Target descriptionhepatitis A virus cellular receptor 1
- Target synonymsHAVcr-1; hepatitis A virus cellular receptor 1 homolog; kidney injury molecule 1; Kim1; KIM-1; t cell immunoglobulin and mucin domain-containing protein 1; TIMD-1
- HostRabbit
- IsotypeIgG
- Protein IDO54947
- Protein NameHepatitis A virus cellular receptor 1 homolog
- Scientific DescriptionBoster Bio Anti-TIM 1/HAVCR1 Antibody catalog # PA1632. Tested in IHC, WB applications. This antibody reacts with Rat. The brand Picoband indicates this is a premium antibody that guarantees superior quality, high affinity, and strong signals with minimal background in Western blot applications. Only our best-performing antibodies are designated as Picoband, ensuring unmatched performance.
- ReactivityRat
- Storage Instruction-20°C,2°C to 8°C
- UNSPSC12352203