Human Anti-APP Recombinant Antibody (clone 266) (CAT#: HPAB-1640-FY)

This product is a recombinant antibody that recognizes APP. The monoclonal antibody 266 reacts with the epitope of APP.


Specific Inquiry
  • Size:
  • Conjugation:
  • Endotoxin:
  • Purity:
  • Fc Engineering:
  • Published Data
  • Gene Expression
  • Datasheet
  • MSDS
  • COA
RIA

Figure 1 Brain injection and clearance of 125I-Aβ1-40 after peripheral administration of anti-Aβ antibodies in mice.

Figure 1 Brain injection and clearance of 125I-Aβ1-40 after peripheral administration of anti-Aβ antibodies in mice.

Timecourseofelimination of 125I-A from brains 120 h after intraperitoneal administration of 10D5, 266, or LB509 as a control IgG.

Yamada, K., Yabuki, C., Seubert, P., Schenk, D., Hori, Y., Ohtsuki, S., ... & Iwatsubo, T. (2009). Aβ immunotherapy: intracerebral sequestration of Aβ by an anti-Aβ monoclonal antibody 266 with high affinity to soluble Aβ. Journal of Neuroscience, 29(36), 11393-11398.

RIA

Figure 2 Brain injection and clearance of 125I-Aβ1-40 after peripheral administration of anti-Aβ antibodies in mice.

Figure 2 Brain injection and clearance of 125I-Aβ1-40 after peripheral administration of anti-Aβ antibodies in mice.

The remaining 125I-A at 60 min after microinjection of 125I-Aβ at 1, 24, or 120 h after intraperitoneal administration of 266 or LB509.

Yamada, K., Yabuki, C., Seubert, P., Schenk, D., Hori, Y., Ohtsuki, S., ... & Iwatsubo, T. (2009). Aβ immunotherapy: intracerebral sequestration of Aβ by an anti-Aβ monoclonal antibody 266 with high affinity to soluble Aβ. Journal of Neuroscience, 29(36), 11393-11398.

ELISA

Figure 3 Differential extraction of brains of APP transgenic mice following peripheral administration of anti-Aβ antibodies.

Figure 3 Differential extraction of brains of APP transgenic mice following peripheral administration of anti-Aβ antibodies.

The levels of monomer Aβ1-40 in the RIPA fractions of 4-month-old A7 mice 120 h after intraperitoneal administration of 266 or LB509 were quantitated by ELISA with (shaded) or without (blank) immunodepletion by protein G.

Yamada, K., Yabuki, C., Seubert, P., Schenk, D., Hori, Y., Ohtsuki, S., ... & Iwatsubo, T. (2009). Aβ immunotherapy: intracerebral sequestration of Aβ by an anti-Aβ monoclonal antibody 266 with high affinity to soluble Aβ. Journal of Neuroscience, 29(36),1393-11398.

ELISA

Figure 4 Differential extraction of brains of APP transgenic mice following peripheral administration of anti-Aβ antibodies.

Figure 4 Differential extraction of brains of APP transgenic mice following peripheral administration of anti-Aβ antibodies.

The levels of monomer Aβ1-42 in the RIPA fractions of 4-month-old A7 mice 120 h after intraperitoneal administration of 266 or LB509 were quantitated by ELISA with (shaded) or without (blank) immunodepletion by protein G.

Yamada, K., Yabuki, C., Seubert, P., Schenk, D., Hori, Y., Ohtsuki, S., ... & Iwatsubo, T. (2009). Aβ immunotherapy: intracerebral sequestration of Aβ by an anti-Aβ monoclonal antibody 266 with high affinity to soluble Aβ. Journal of Neuroscience, 29(36),1393-11398.

IB

Figure 5 The total Aβ and its precursor C99 in the RIPA fractions were analyzed by immunoblotting with 82E1 after immunoprecipitation with the same antibody.

Figure 5 The total Aβ and its precursor C99 in the RIPA fractions were analyzed by immunoblotting with 82E1 after immunoprecipitation with the same antibody.

Yamada, K., Yabuki, C., Seubert, P., Schenk, D., Hori, Y., Ohtsuki, S., ... & Iwatsubo, T. (2009). Aβ immunotherapy: intracerebral sequestration of Aβ by an anti-Aβ monoclonal antibody 266 with high affinity to soluble Aβ. Journal of Neuroscience, 29(36),1393-11398.

Activ

Figure 6 Chronic administration of anti-Aβ mAbs increased plasma Aβ levels in J20 mice.

Figure 6 Chronic administration of anti-Aβ mAbs increased plasma Aβ levels in J20 mice.

Free Aβ1-x, i.e. material still present in the supernatant following PrG incubation, was significantly increased in J20 mice that received 1C22, compared to 46-4- and m266-treated J20 mice.

Mably, A. J., Liu, W., Mc Donald, J. M., Dodart, J. C., Bard, F., Lemere, C. A., ... & Walsh, D. M. (2015). Anti-Aβ antibodies incapable of reducing cerebral Aβ oligomers fail to attenuate spatial reference memory deficits in J20 mice. Neurobiology of disease, 82, 372-384.

Activ

Figure 7 Chronic administration of anti-Aβ mAbs increased plasma Aβ levels in J20 mice.

Figure 7 Chronic administration of anti-Aβ mAbs increased plasma Aβ levels in J20 mice.

Antibody-bound Aβ1-x was significantly increased in m266-treated J20 mice, compared to 46-4- and 1C22-treated J20 mice.

Mably, A. J., Liu, W., Mc Donald, J. M., Dodart, J. C., Bard, F., Lemere, C. A., ... & Walsh, D. M. (2015). Anti-Aβ antibodies incapable of reducing cerebral Aβ oligomers fail to attenuate spatial reference memory deficits in J20 mice. Neurobiology of disease, 82, 372-384.


Specifications

  • Host Species
  • Human
  • Derivation
  • Humanized
  • Type
  • Humanized IgG
  • Specificity
  • Human APP
  • Species Reactivity
  • Human
  • Clone
  • 266
  • Applications
  • RIA, ELISA, IB, Activ
  • Related Disease
  • Alzheimer's disease

Product Property

  • Purity
  • >95% as determined by SDS-PAGE and HPLC analysis
  • Concentration
  • Please refer to the vial label for the specific concentration.
  • Buffer
  • PBS
  • Preservative
  • No preservatives
  • Storage
  • Centrifuge briefly prior to opening vial. Store at +4°C short term (1-2 weeks). Aliquot and store at -20°C long term. Avoid repeated freeze/thaw cycles.

Applications

  • Application Notes
  • The APP antibody has been reported in applications of Radioimmunoassay, Enzyme-linked Immunosorbent Assay, Immunoblotting, Activation.

Target

  • Alternative Names
  • Amyloid Beta Precursor Protein; Amyloid Beta (A4) Precursor Protein; Alzheimer Disease Amyloid Protein; Cerebral Vascular Amyloid Peptide; Amyloid Precursor Protein; Peptidase Nexin-II; Protease Nexin-II; PreA4; PN-II; ABPP; APPI; CVAP; AD1; Beta-Amyloid Precursor Protein

Product Notes

This is a product of Creative Biolabs' Hi-Affi™ recombinant antibody portfolio, which has several benefits including:

• Increased sensitivity
• Confirmed specificity
• High repeatability
• Excellent batch-to-batch consistency
• Sustainable supply
• Animal-free production

See more details about Hi-Affi™ recombinant antibody benefits.

Downloads

Download resources about recombinant antibody development and antibody engineering to boost your research.

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ADCC Enhanced Antibody

CAT Product Name Application Type
AFC-TAB-225 Afuco™ Anti-APP ADCC Recombinant Antibody (Bapineuzumab), ADCC Enhanced FuncS, IF, Neut, ELISA, FC ADCC enhanced antibody
AFC-TAB-228 Afuco™ Anti-APP ADCC Recombinant Antibody (Solanezumab), ADCC Enhanced FuncS, IF, Neut, ELISA, FC ADCC enhanced antibody
AFC-TAB-229 Afuco™ Anti-APP ADCC Recombinant Antibody (Gantenerumab), ADCC Enhanced FuncS, IF, Neut, ELISA, FC, IP ADCC enhanced antibody
AFC-TAB-227 Afuco™ Anti-APP ADCC Recombinant Antibody (Ponezumab), ADCC Enhanced ELISA, IP, FC, FuncS, Neut ADCC enhanced antibody
AFC-TAB-226 Afuco™ Anti-APP ADCC Recombinant Antibody (Crenezumab), ADCC Enhanced IF, IP, Neut, FuncS, ELISA ADCC enhanced antibody

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For Research Use Only. Not For Clinical Use.

For research use only. Not intended for any clinical use. No products from Creative Biolabs may be resold, modified for resale or used to manufacture commercial products without prior written approval from Creative Biolabs.

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