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HEPACAM2 Antibody

Catalog Number: orb1819360

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100 μg$ 500.00
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DispatchUsually dispatched within 2-4 weeks
Product Properties
Catalog Numberorb1819360
CategoryAntibodies
DescriptionAnti-HEPACAM2 Antibody. Tested in ELISA, IHC, WB applications. This antibody reacts with Human.
ClonalityPolyclonal
Species/HostRabbit
IsotypeIgG
ConjugationUnconjugated
ReactivityHuman
Form/AppearanceLyophilized
ConcentrationAdding 0.2 ml of distilled water will yield a concentration of 500 μg/ml.
PurificationImmunogen affinity purified.
ImmunogenE.coli-derived human HEPACAM2 recombinant protein (Position: G31-K345). Human HEPACAM2 shares 88.6% amino acid (aa) sequence identity with mouse HEPACAM2.
UniProt IDA8MVW5
MW65 kDa
Tested applicationsELISA, IHC, WB
Application notesWestern blot, 0.1-0.25 μg/ml, Human Immunohistochemistry, 2-5 μg/ml, Human ELISA, 0.1-0.5 μg/ml, -. Adding 0.2 ml of distilled water will yield a concentration of 500 μg/ml
Cross ReactivityNo cross reactivity with other proteins.
Antibody TypePrimary Antibody
StorageMaintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles.
Alternative names70 kDa ribosomal protein S6 kinase 1 antibody, KS6
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NoteFor research use only
Images
HEPACAM2 Antibody

IHC analysis of HEPACAM2 using anti-HEPACAM2 antibody. HEPACAM2 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 µg/ml rabbit anti-HEPACAM2 Antibody overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit with DAB as the chromogen.

HEPACAM2 Antibody

IHC analysis of HEPACAM2 using anti-HEPACAM2 antibody. HEPACAM2 was detected in a paraffin-embedded section of human pancreas ductal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 µg/ml rabbit anti-HEPACAM2 Antibody overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit with DAB as the chromogen.

HEPACAM2 Antibody

IHC analysis of HEPACAM2 using anti-HEPACAM2 antibody. HEPACAM2 was detected in a paraffin-embedded section of human testicular seminoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 µg/ml rabbit anti-HEPACAM2 Antibody overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit with DAB as the chromogen.

HEPACAM2 Antibody

Western blot analysis of HEPACAM2 using anti-HEPACAM2 antibody. 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 30 ug of sample under reducing conditions. Lane 1: human K562 whole cell lysates, Lane 2: human HEL whole cell lysates, Lane 3: human Caco-2 whole cell lysates, Lane 4: human SH-SY5Y whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA 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-HEPACAM2 antigen affinity purified polyclonal antibody at 0.25 µg/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 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit with Tanon 5200 system. A specific band was detected for HEPACAM2 at approximately 65 kDa. The expected band size for HEPACAM2 is at 51 kDa.

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