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OP44 Anti-APC (Ab-1) Mouse mAb (FE9)

Anti-APC (Ab-1), mouse monoclonal, clone FE9, recognizes full length APC (p300) in HCT116 cells and truncated APC (p147) in SW480 cells. It is validated for Western botting.

Anti-APC (Ab-1) Mouse mAb (FE9) MSDS (material safety data sheet) or SDS, CoA and CoQ, dossiers, brochures and other available documents.

同义词: Anti-Adenomatous Polyposis Coli

OP44
Purchase on Sigma-Aldrich

概述

Replacement Information

重要规格表

Species ReactivityHostAntibody Type
H, M, RMMonoclonal Antibody

Products

产品目录编号包装 数量 / 包装
OP44-100UGCN 塑胶安瓿;塑胶针药瓶 100 μg
Description
OverviewRecognizes full length APC (p300) in HCT116 cells and truncated APC (p147) in SW480 cells.
  • Antibody Target Gene Symbol: APC
  • Target Synonym: AI047805, Apc7, AU020952, AW124434, BTPS2, DP2, DP2.5, DP3, Familial adenomatous polyposis, FAP, GS, Min, RATAPC
  • Entrez Gene Name: adenomatous polyposis coli
  • Hu Entrez ID: 324 (Related Antibodies: OP80, ST1150, OP62, OP47L)
  • Mu Entrez ID: 11789
  • Rat Entrez ID: 24205
    		•
    Catalogue NumberOP44
    Brand Family Calbiochem®
    SynonymsAnti-Adenomatous Polyposis Coli
    References
    ReferencesKoetsier, P. A., et al. 1993. BioTechniques 15, 258.
    Smith, K. J., et al. 1993. Proc. Natl. Acad. Sci., USA 90, 2846.
    Su, L.-K., et al. 1993. Can. Res. 53, 2728.
    Boynton, R. F., et al. 1992. Proc. Natl. Acad. Sci. USA 89, 3385.
    D'Amico, D., et al. 1992. Cancer Res. 52, 1996.
    Fearon, E. R., and Jones, P. A., 1992. FASEB J. 6, 2783.
    Miyoshi, Y., et al. 1992. Proc. Natl. Acad. Sci. USA 89, 4452.
    Powell, S. M., et al. 1992. Nature 359, 235.
    Groden, J., et al. 1991. Cell 66, 589.
    Kinzler, K. W., et al. 1991. Science 253, 661.
    Nishisho, I., et al. 1991. Science 253, 665.
    Product Information
    FormLiquid
    FormulationIn 50 mM sodium phosphate buffer, pH 7.5, 0.2% gelatin.
    Positive controlHCT116 cells for p300, SW480 cells for truncated APC (p147)
    Preservative≤0.1% sodium azide
    Quality LevelMQ100
    Applications
    Key Applications Immunoblotting (Western Blotting)
    Application NotesImmunoblotting (1 µg/ml, see comments)
    Application CommentsFull-length p300APC can be observed by western blot and various truncated forms of the APC protein have been observed in tumors obtained from sporadic colorectal cancer patients and in lymphocytes obtained from FAP patients. SW480 cells, which contain a mutation at codon 1338 of APC and express a truncated APC protein of 147 kDa, and HCT116 cells, which express full length APC, are available from ATCC for use as positive controls in western blotting with APC (Ab-1). Antibody should be titrated for optimal results in indivual systems.

    IMMUNOBLOTTING PROCEDURE

    Materials:
    1. Equipment
    Electrophoresis apparatus and Rocker platform

    2. Reagents and Solutions
    • Anti-APC (Ab-1) Mouse mAb (FE9), Cat. No. OP44
    • Secondary antibody (e.g. Goat Anti-Mouse IgG, H & L chain specific Peroxidase conjugate, Cat. No. 401215)
    • Chemiluminescent detection system
    • 1x Laemmli Sample Buffer: 60 mM Tris-Cl, pH 6.8, 2% SDS, 10% Glycerol, 100 mM DTT, 0.001% Bromophenol Blue
    • Laemmli Running Buffer: 25 mM Tris base, 192 mM Glycine, 0.1% SDS
    • 3% Low Melt Agarose (i.e. SeaPlaque from FMC) in TBE/0.1% SDS: TBE: 89 mM Tris base, 89 mM Boric acid, 2 mM EDTA pH 8.0
    • Tris-buffered saline (TBS) pH 7.6: 20 mM Tris base, 137 mM NaCl, pH to 7.6 with HCl
    • TBS/0.04% SDS
    • TBS/0.1% Tween®-20 detergent (TBST)
    • 10% Non-fat Dry Milk in TBST
    • 5% Non-fat Dry Milk in TBST

    Agarose Gel and Capillary Blotting Procedures:
    1) Lyse cells in 1x Laemmli Sample Buffer. For adherent cells, lyse a 10 cm plate that is 80 to 90% confluent in 2 ml of sample buffer added directly to cells on the plate. Final protein concentration is approximately 1 mg/ml.

    2) Electrophorese 50-100 µg of total lysate protein on a 3% low melt agarose gel made in TBE/0.1% SDS. Use a vertical polyacrylamide gel apparatus with 1 mm spacers. Pour a 1 cm 15% acrylamide plug. Prewarm the gel apparatus to 37°C before pouring the agarose gel. Pour the molten agarose while it is still 65° to 70°C. There is no stacking gel. Use Laemmli running buffer. Run the gel at 15V per centimeter until the proteins in the 40 kDa to 60 kDa range have migrated off the bottom of the gel.

    3) Transfer the proteins overnight onto a PVDF membrane by downward capillary transfer as outlined below using TBS/0.04% SDS as the transfer buffer:

    a. On a 2 inch stack of blotting paper or paper towels, place three pieces of gel-sized Whatman 3 MM chromatography paper with the top piece pre-soaked in transfer buffer.

    b. Place a pre-soaked, gel-sized piece of PVDF membrane on top of the Whatman papers.

    c. Place the gel on top of the membrane and cover the exposed papers with plastic wrap.

    d. Place two gel-sized pieces of pre-soaked Whatman 3MM paper on top of the gel.

    e. On opposite sides of the blotting stack place a tray containing transfer buffer.

    f. Lay two pre-soaked, long pieces of Whatman paper across the top of the gel set up so that the ends are submerged in the trays containing transfer buffer.

    g. Cover the entire set-up with plastic wrap and allow the transfer to go overnight.

    4) After overnight transfer, mark the position of protein standards on the PVDF membrane with a pencil. The membrane is then incubated for 1 h in 10% non-fat dry milk in TBST at room temperature with rocking. Use about 1 ml of solution per cm2 of membrane.

    5) Incubate the membrane with 1 µg/ml of APC antibody in 5% non-fat dry milk in TBST for 2 h at room temperature with rocking.

    6) Wash the membrane 3 times, 10 min each, in TBST at room temperature with rocking.

    7) Incubate the membrane with 30 ng/ml of HRP conjugated goat anti-mouse IgG heavy and light chain antibody in 5% non-fat dry milk in TBST at room temperature for 1 h.

    8) Wash the membrane 6 times, 15 min each, in TBST at room temperature with rocking.

    9) Develop the membrane using chemiluminescent detection reagents according to manufacturers instructions.

    10) Expose the membrane to film for 30 min. Adjust subsequent exposure times (from 30 s up to 24 h) as necessary.
    Biological Information
    Immunogena synthetic peptide corresponding to the N-terminal 35 amino acids of APC
    CloneFE9
    HostMouse
    IsotypeIgG₁
    Species Reactivity
    • Human
    • Mouse
    • Rat
    Antibody TypeMonoclonal Antibody
    Concentration Label Please refer to vial label for lot-specific concentration
    Physicochemical Information
    Dimensions
    Materials Information
    Toxicological Information
    Safety Information according to GHS
    Safety Information
    Product Usage Statements
    Storage and Shipping Information
    Ship Code Blue Ice Only
    Toxicity Standard Handling
    Storage +2°C to +8°C
    Do not freeze Yes
    Packaging Information
    Transport Information
    Supplemental Information
    Specifications
    Global Trade Item Number
    产品目录编号 GTIN
    OP44-100UGCN 04055977227130

    Documentation

    Anti-APC (Ab-1) Mouse mAb (FE9) MSDS

    职位

    物料安全数据表 (MSDS) 

    Anti-APC (Ab-1) Mouse mAb (FE9) 分析证书

    标题批号
    OP44

    参考

    参考信息概述
    Koetsier, P. A., et al. 1993. BioTechniques 15, 258.
    Smith, K. J., et al. 1993. Proc. Natl. Acad. Sci., USA 90, 2846.
    Su, L.-K., et al. 1993. Can. Res. 53, 2728.
    Boynton, R. F., et al. 1992. Proc. Natl. Acad. Sci. USA 89, 3385.
    D'Amico, D., et al. 1992. Cancer Res. 52, 1996.
    Fearon, E. R., and Jones, P. A., 1992. FASEB J. 6, 2783.
    Miyoshi, Y., et al. 1992. Proc. Natl. Acad. Sci. USA 89, 4452.
    Powell, S. M., et al. 1992. Nature 359, 235.
    Groden, J., et al. 1991. Cell 66, 589.
    Kinzler, K. W., et al. 1991. Science 253, 661.
    Nishisho, I., et al. 1991. Science 253, 665.
    数据表

    Note that this data sheet is not lot-specific and is representative of the current specifications for this product. Please consult the vial label and the certificate of analysis for information on specific lots. Also note that shipping conditions may differ from storage conditions.

    Revision10-May-2010 RFH
    SynonymsAnti-Adenomatous Polyposis Coli
    ApplicationImmunoblotting (1 µg/ml, see comments)
    DescriptionProtein G purified mouse monoclonal antibody generated by immunizing mice with the specified immunogen and fusing splenocytes with SP40 cells. Recognizes the ~300 kDa APC protein as well as a variety of truncated forms.
    BackgroundColon cancer generally occurs sporadically although there is clear genetic predisposition in some families. Familial Adenomatous Polyposis Coli (FAP) is an autosomal dominantly inherited disorder that exhibits 80 to 100% penetrance and predisposes to colon cancer. The gene responsible for FAP has been assigned to chromosome 5q21, a region that is often lost in tumors from patients with sporadic colorectal cancer. Recently, a gene called APC, for adenomatous polyposis coli, from the 5q21 locus was isolated and shown to contain mutations in DNA prepared from tumors of patients with sporadic colorectal cancer and in germ line DNA and tumor DNA from FAP patients. In 79 unrelated patients with FAP, mutations in APC were found in 67% of the cases; and 49 of the 53 mutations were either small deletions/insertion or were point mutations that introduced stop codons into the reading frame. Furthermore, APC mutations have been found in the earliest tumors that could be analyzed (0.5 cm diameter) and the mutation frequency remained constant as tumors progressed from benign to malignant stages. Analysis of the APC protein demonstrates that inactivating mutations result in stable truncated proteins that can be identified in colon tumors from both FAP and sporadic colon cancer patients as well as in constitutional cells of FAP patients. Loss of heterozygosity at the APC locus has also been reported for esophageal cancer and lung cancer.
    HostMouse
    Immunogena synthetic peptide corresponding to the N-terminal 35 amino acids of APC
    CloneFE9
    IsotypeIgG₁
    Specieshuman, mouse, rat
    Positive controlHCT116 cells for p300, SW480 cells for truncated APC (p147)
    FormLiquid
    FormulationIn 50 mM sodium phosphate buffer, pH 7.5, 0.2% gelatin.
    Concentration Label Please refer to vial label for lot-specific concentration
    Preservative≤0.1% sodium azide
    CommentsFull-length p300APC can be observed by western blot and various truncated forms of the APC protein have been observed in tumors obtained from sporadic colorectal cancer patients and in lymphocytes obtained from FAP patients. SW480 cells, which contain a mutation at codon 1338 of APC and express a truncated APC protein of 147 kDa, and HCT116 cells, which express full length APC, are available from ATCC for use as positive controls in western blotting with APC (Ab-1). Antibody should be titrated for optimal results in indivual systems.

    IMMUNOBLOTTING PROCEDURE

    Materials:
    1. Equipment
    Electrophoresis apparatus and Rocker platform

    2. Reagents and Solutions
    • Anti-APC (Ab-1) Mouse mAb (FE9), Cat. No. OP44
    • Secondary antibody (e.g. Goat Anti-Mouse IgG, H & L chain specific Peroxidase conjugate, Cat. No. 401215)
    • Chemiluminescent detection system
    • 1x Laemmli Sample Buffer: 60 mM Tris-Cl, pH 6.8, 2% SDS, 10% Glycerol, 100 mM DTT, 0.001% Bromophenol Blue
    • Laemmli Running Buffer: 25 mM Tris base, 192 mM Glycine, 0.1% SDS
    • 3% Low Melt Agarose (i.e. SeaPlaque from FMC) in TBE/0.1% SDS: TBE: 89 mM Tris base, 89 mM Boric acid, 2 mM EDTA pH 8.0
    • Tris-buffered saline (TBS) pH 7.6: 20 mM Tris base, 137 mM NaCl, pH to 7.6 with HCl
    • TBS/0.04% SDS
    • TBS/0.1% Tween®-20 detergent (TBST)
    • 10% Non-fat Dry Milk in TBST
    • 5% Non-fat Dry Milk in TBST

    Agarose Gel and Capillary Blotting Procedures:
    1) Lyse cells in 1x Laemmli Sample Buffer. For adherent cells, lyse a 10 cm plate that is 80 to 90% confluent in 2 ml of sample buffer added directly to cells on the plate. Final protein concentration is approximately 1 mg/ml.

    2) Electrophorese 50-100 µg of total lysate protein on a 3% low melt agarose gel made in TBE/0.1% SDS. Use a vertical polyacrylamide gel apparatus with 1 mm spacers. Pour a 1 cm 15% acrylamide plug. Prewarm the gel apparatus to 37°C before pouring the agarose gel. Pour the molten agarose while it is still 65° to 70°C. There is no stacking gel. Use Laemmli running buffer. Run the gel at 15V per centimeter until the proteins in the 40 kDa to 60 kDa range have migrated off the bottom of the gel.

    3) Transfer the proteins overnight onto a PVDF membrane by downward capillary transfer as outlined below using TBS/0.04% SDS as the transfer buffer:

    a. On a 2 inch stack of blotting paper or paper towels, place three pieces of gel-sized Whatman 3 MM chromatography paper with the top piece pre-soaked in transfer buffer.

    b. Place a pre-soaked, gel-sized piece of PVDF membrane on top of the Whatman papers.

    c. Place the gel on top of the membrane and cover the exposed papers with plastic wrap.

    d. Place two gel-sized pieces of pre-soaked Whatman 3MM paper on top of the gel.

    e. On opposite sides of the blotting stack place a tray containing transfer buffer.

    f. Lay two pre-soaked, long pieces of Whatman paper across the top of the gel set up so that the ends are submerged in the trays containing transfer buffer.

    g. Cover the entire set-up with plastic wrap and allow the transfer to go overnight.

    4) After overnight transfer, mark the position of protein standards on the PVDF membrane with a pencil. The membrane is then incubated for 1 h in 10% non-fat dry milk in TBST at room temperature with rocking. Use about 1 ml of solution per cm2 of membrane.

    5) Incubate the membrane with 1 µg/ml of APC antibody in 5% non-fat dry milk in TBST for 2 h at room temperature with rocking.

    6) Wash the membrane 3 times, 10 min each, in TBST at room temperature with rocking.

    7) Incubate the membrane with 30 ng/ml of HRP conjugated goat anti-mouse IgG heavy and light chain antibody in 5% non-fat dry milk in TBST at room temperature for 1 h.

    8) Wash the membrane 6 times, 15 min each, in TBST at room temperature with rocking.

    9) Develop the membrane using chemiluminescent detection reagents according to manufacturers instructions.

    10) Expose the membrane to film for 30 min. Adjust subsequent exposure times (from 30 s up to 24 h) as necessary.
    Storage +2°C to +8°C
    Do Not Freeze Yes
    Toxicity Standard Handling
    ReferencesKoetsier, P. A., et al. 1993. BioTechniques 15, 258.
    Smith, K. J., et al. 1993. Proc. Natl. Acad. Sci., USA 90, 2846.
    Su, L.-K., et al. 1993. Can. Res. 53, 2728.
    Boynton, R. F., et al. 1992. Proc. Natl. Acad. Sci. USA 89, 3385.
    D'Amico, D., et al. 1992. Cancer Res. 52, 1996.
    Fearon, E. R., and Jones, P. A., 1992. FASEB J. 6, 2783.
    Miyoshi, Y., et al. 1992. Proc. Natl. Acad. Sci. USA 89, 4452.
    Powell, S. M., et al. 1992. Nature 359, 235.
    Groden, J., et al. 1991. Cell 66, 589.
    Kinzler, K. W., et al. 1991. Science 253, 661.
    Nishisho, I., et al. 1991. Science 253, 665.