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APOE antibody - N-terminal region (ARP54283_P050)

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100 ul
$289.00
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Gene Symbol:
APOE
NCBI Gene Id:
348
Official Gene Full Name:
Apolipoprotein E
Protein Name:
Apolipoprotein E
Swissprot Id:
P02649
Protein Accession #:
NP_000032
Nucleotide Accession #:
NM_000041
Alias Symbols:
AD2, MGC1571, apoprotein, LPG, LDLCQ5
Description of Target:
Chylomicron remnants and very low density lipoprotein (VLDL) remnants are rapidly removed from the circulation by receptor-mediated endocytosis in the liver. Apolipoprotein E, a main apoprotein of the chylomicron, binds to a specific receptor on liver cells and peripheral cells. ApoE is essential for the normal catabolism of triglyceride-rich lipoprotein constituents. Defects in apolipoprotein E result in familial dysbetalipoproteinemia, or type III hyperlipoproteinemia (HLP III), in which increased plasma cholesterol and triglycerides are the consequence of impaired clearance of chylomicron and VLDL remnants.Chylomicron remnants and very low density lipoprotein (VLDL) remnants are rapidly removed from the circulation by receptor-mediated endocytosis in the liver. Apolipoprotein E, a main apoprotein of the chylomicron, binds to a specific receptor on liver cells and peripheral cells. ApoE is essential for the normal catabolism of triglyceride-rich lipoprotein constituents. The APOE gene is mapped to chromosome 19 in a cluster with APOC1 and APOC2. Defects in apolipoprotein E result in familial dysbetalipoproteinemia, or type III hyperlipoproteinemia (HLP III), in which increased plasma cholesterol and triglycerides are the consequence of impaired clearance of chylomicron and VLDL remnants. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.
Protein Size (# AA):
317
Molecular Weight:
34kDa
Host:
Rabbit
Clonality:
Polyclonal
Purification:
Affinity Purified
Application:
WB, IHC
Tissue Tool:
Find tissues and cell lines supported by DNA array analysis to express APOE.
RNA Seq:
Find tissues and cell lines supported by RNA-seq analysis to express APOE.
Immunogen:
The immunogen is a synthetic peptide directed towards the N terminal region of human APOE
Species Reactivity:
Human
Predicted Homology Based on Immunogen Sequence:
Human: 100%
Complete computational species homology data:
Anti-APOE (ARP54283_P050)
Peptide Sequence:
Synthetic peptide located within the following region: KVLWAALLVTFLAGCQAKVEQAVETEPEPELRQQTEWQSGQRWELALGRF
Product Format:
Liquid. Purified antibody supplied in 1x PBS buffer with 0.09% (w/v) sodium azide and 2% sucrose.
Reconstitution and Storage:
For short term use, store at 2-8C up to 1 week. For long term storage, store at -20C in small aliquots to prevent freeze-thaw cycles.
Concentration:
Batch dependent within range: 100 ul at 0.5 - 1 mg/ml
Protein Interactions:
LCAT; ARFGAP1; ALB; C19orf52; LOXL4; PRAM1; MID1IP1; ANKH; FBXL12; FXYD7; ECSIT; PDCD4; IFIT5; MAST1; EPN2; PLEKHA6; CDC37; IQSEC1; LONP1; TYRO3; PRDX2; ST13; RPL4; RHEB; PSEN1; HTRA1; PCMT1; ZNF558; NOS3; IFIT3; GCDH; FOXG1; FARSA; ELAVL1; CYP2C18; CYP2C
Blocking Peptide:
For anti-APOE (ARP54283_P050) antibody is Catalog # AAP54283 (Previous Catalog # AAPP31032)
Datasheets / Downloads:
Printable datasheet for anti-APOE (ARP54283_P050) antibody
Additional Information:
IHC Information: Human Adrenal: Formalin-Fixed, Paraffin-Embedded (FFPE)
IHC Information: Human Kidney: Formalin-Fixed, Paraffin-Embedded (FFPE)
Target Reference:
Ho,R.C., (2008) Am J Geriatr Psychiatry 16 (6), 519-522
Publications:

Rohn, T. T., Catlin, L. W., Coonse, K. G. & Habig, J. W. Identification of an amino-terminal fragment of apolipoprotein E4 that localizes to neurofibrillary tangles of the Alzheimer’s disease brain. Brain Res. 1475, 106-15 (2012). WB, IHC, ICC/IF, Human 22902767

Rohn, T. T., Day, R. J., Sheffield, C. B., Rajic, A. J. & Poon, W. W. Apolipoprotein E pathology in vascular dementia. Int. J. Clin. Exp. Pathol. 7, 938-47 (2014). ICC/IF, Human 24696712

Additional Product Images:

Customer Reviews for APOE Antibody (ARP54283_P050) tested with rat brain tissue in Immunohistochemistry

CAT#: ARP54283

submitted by:
Thomas Van Groen PhD
University of Alabama
Neuroscience lab
Version: 2.0
Date: 17 Oct 2005

Immunohistochemistry:

CITRATE PRETREATMENT

PRETREATMENTS WITH CITRATE SOLUTION

FOR WATER BATH

1) Fill water bath with warm water, set it for 85oC.

2) Put square glass jar (filled with the citrate solution) on a rack in the water bath, so it gets heated to the appropriate temperature, i.e., 85oC.

3) Put a tissue rack with the to be treated tissue in the water bath for 30 minutes.

4) Take it out and let it cool down in either citrate or phosphate buffer.

FOR MICROWAVE

1) Put plastic tray filled with some water (about 3 cm high) in microwave.

2) Put glass tray with citrate buffer, with rack (new rack) with sections in glass tray.

3) Heat for 3 min at 440 Watt setting.

4) Let it cool down (20 min) and rinse in buffer.

CITRATE SOLUTION:

0.05 M NaCitrate solution; add 14.7 g of NaCitrate-2 hydrate to 1 liter of dH2O,
NOTE: adjust pH. to pH 6.0

IMMUNO:

1. Pretreat tissue in hot citrate solution (see protocol).

2. Use small (4 x 6) tray; rinse tissue 3 X 5 min each in TBS-T (Tris Buffered Saline + 0.5% Triton; pH 7.6). Approximately 20 ml/tray.

3. Put in primary antibody (mouse anti-APP at 1:5000; Chemicon) for 18 h at room temperature (20 C) in TBS-T on a shaker table in the dark.
Mouse anti-APP at 1:5000
2 ml antibody in 10 ml TBS-T

4. Rinse 3 X (5 min each) in TBS-T; approximately 20 ml.

5. Put in secondary antibody (Goat anti-mouse*biotin at 1:400; Sigma) for 2 h.
Goat anti-mouse*biotin at 1:400
25 ml antibody in 10 ml TBS-T

6. Rinse 3 X in TBS-T (5 min each); approximately 20 ml.

7. Put in ExtrAvidin® (at 1:1000) for 2 h.
ExtrAvidin® at 1:1000
10 ml antibody in 10 ml TBS-T

8. Rinse 3 X in TBS-T (5 min each); approximately 20 ml.

9. Put in metal-intensified DAB for approximately 3 min.
-20 ml 0.05 M Tris Buffer pH 7.6
-5 mg DAB
-1 ml of a saturated Ni ammonium sulfate solution
-15 ml 30 % H2O2

10. Rinse excess DAB out with Naphosphate buffer, mount tissue.

NOTE: Filter solution before use. Anything that DAB comes in contact with should be neutralized with a diluted bleach solution. DAB is a SUSPECTED CARCINOGEN; you should/can use gloves and particle mask.

TRIS BUFFERED SALINE + TRITON 0.5 M at pH 7.6

To make 2 liters:
Trizma HCl 12.12 g
Trizma Base 2.78 g
NaCl 58.4 g
Triton 5 ml

Product Review: APOE antibody - N-terminal region (ARP54283_P050) using Human brain cell homogenates in Western Blot

Product Page Link: APOE antibody - N-terminal region (ARP54283_P050)

Data provided by Dr. Martin Sadowski of the New York University School of Medicine

"We have done a couple of WB using your polyclonal antibody sample. It detects recombinant human APO E3 and E4 with great sensitivity and they are amazingly clean (i.e. do not produce non-specific staining on WB of brain and cell homogenates).

Sample type: Human brain cell homogenates

Primary Antibody Dilution: 1:000

Secondary Antibody Dilution: 1:2000

Product Protocols: APOE antibody tested by IHC with Human Liver Tissue ARP54283_P050

Aviva Systems Biology is the original manufacturer of this APOE antibody.
Product Datasheet Link: APOE antibody ARP54283_P050

Rabbit Anti-APOE Antibody
Catalog Number: ARP54283_P050
Formalin Fixed Paraffin Embedded Tissue: Human Liver Tissue
Observed Staining: Cytoplasm and membrane of hepatocytes
Primary Antibody Concentration: 1/600
Other Working Concentrations: 1/100
Secondary Antibody: Donkey anti-Rabbit-Cy3
Secondary Antibody Concentration: 1:200
Magnification: 20X
Exposure Time: 0.5 – 2.0 sec

Left to right:
DAPI, APOE Ab, Merge

Control Image
Control Antibody: Normal Rabbit IgG
Control Antibody Concentration: 1:100

Left to right:
DAPI, Rabbit IgG, Merge

Protocol:
1. Normal adult Human Liver Tissue was formalin fixed, embedded in paraffin wax, sectioned at 6 micron thickness and put on histological slides.
2. After deparaffinization and rehydration, the low pH, heat-induced antigen retrieval method utilizing Sodium Citrate buffer was performed.
3. The blocking buffer was 5% normal goat serum.
4. Primary antibodies was diluted in antibody dilution buffer (1% Normal Donkey Serum) to the final testing dilution (1:100, 1:600, 1:1200).
5. The appropriate anti-rabbit fluorescent-conjugated (Rhodamine:red or FITC:green) secondary antibody was applied and nuclei will be counterstained with DAPI (blue).
6. A Negative control utilized a nonspecific rabbit IgG staining the same normal adult Human Liver Tissue.

 
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