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Validation Data Gallery

  • Mouse IgG (anti-Lamin; 66095-1-Ig) was conjugated with NHS-Azide (lane 1) and then with DBCO-Oligo (lane 2). Post conjugation clean-up was done using CleanAb Kit for Mouse IgG (lanes 3-5). Excess oligo was successfully removed as shown in SYBR Gold DNA staining and IgG eluted with high recovery (~70%) at neutral pH (lane 4). Desalting was done with Zeba spin desalting columns (lane 5). Only very little IgG remaining on beads (lane 6).

    Mouse IgG (anti-Lamin; 66095-1-Ig) was conjugated with NHS-Azide (lane 1) and then with DBCO-Oligo (lane 2). Post conjugation clean-up was done using CleanAb Kit for Mouse IgG (lanes 3-5). Excess oligo was successfully removed as shown in SYBR Gold DNA staining and IgG eluted with high recovery (~70%) at neutral pH (lane 4). Desalting was done with Zeba spin desalting columns (lane 5). Only very little IgG remaining on beads (lane 6).

  • Mouse IgG (anti-Lamin; 66095-1-Ig) was bound to Mouse CleanAb beads (flowthrough in lane 2), then functionalized on beads with NHS-Azide (flowthrough in lane 3) and then with DBCO-Oligo (flowthrough in lane 4). Excess oligo was successfully removed as shown in SYBR Gold DNA staining and the oligo-conjugated IgG was eluted with high recovery at neutral pH (lane 6). Desalting was done with Zeba spin desalting columns (lane 8). Only very little IgG remaining on beads (lane 9).

    Mouse IgG (anti-Lamin; 66095-1-Ig) was bound to Mouse CleanAb beads (flowthrough in lane 2), then functionalized on beads with NHS-Azide (flowthrough in lane 3) and then with DBCO-Oligo (flowthrough in lane 4). Excess oligo was successfully removed as shown in SYBR Gold DNA staining and the oligo-conjugated IgG was eluted with high recovery at neutral pH (lane 6). Desalting was done with Zeba spin desalting columns (lane 8). Only very little IgG remaining on beads (lane 9).

  • Mouse IgG (anti-Lamin B1 IgG1; 66095-1-Ig) was conjugated with NHS-Azide (lane 1) and then with DBCO-Oligo (lane 2). (left) Post conjugation clean-up was done using CleanAb Kit for rabbit IgG (lanes 3-5). Excess oligo was successfully removed as shown by SYBR Gold DNA staining and IgG eluted with high recovery (~70%) at neutral pH (lane 4). Desalting was done with Zeba spin desalting columns (lane 5). Only very little IgG remaining on beads (lane 6) (right) Post conjugation clean-up was done using Protein A beads (lanes 3-5). Excess oligo was successfully removed as shown by SYBR Gold DNA staining but IgG elution with low pH failed (lane 4). Most IgG remains on beads (lane 6).

    Mouse IgG (anti-Lamin B1 IgG1; 66095-1-Ig) was conjugated with NHS-Azide (lane 1) and then with DBCO-Oligo (lane 2). (left) Post conjugation clean-up was done using CleanAb Kit for rabbit IgG (lanes 3-5). Excess oligo was successfully removed as shown by SYBR Gold DNA staining and IgG eluted with high recovery (~70%) at neutral pH (lane 4). Desalting was done with Zeba spin desalting columns (lane 5). Only very little IgG remaining on beads (lane 6) (right) Post conjugation clean-up was done using Protein A beads (lanes 3-5). Excess oligo was successfully removed as shown by SYBR Gold DNA staining but IgG elution with low pH failed (lane 4). Most IgG remains on beads (lane 6).

  • (left) Mouse IgG (anti-Lamin B1 IgG1; 66095-1-Ig, lane 1) was bound to CleanAb rabbit beads (flowthrough in lane 2), then functionalized on beads with NHS-Azide (flowthrough in lane 3) and then with DBCO-Oligo (flowthrough in lane 4). Excess oligo was successfully removed as shown in SYBR Gold DNA staining and the oligo-conjugated IgG was eluted with high recovery at neutral pH (lane 6). Desalting was done with Zeba spin desalting columns (lane 8). Only very little IgG remaining on beads (lane 9). Note: the CleanAb Elution Buffer can interfere with SDS gels, which can make the CleanAb elution appear washed out. (right) Mouse IgG (anti-Lamin B1 IgG1; 66095-1-Ig, lane 1) was bound to Protein A beads (flowthrough in lane 2), Excess oligo was successfully removed as shown in SYBR Gold DNA staining but the oligo-conjugated IgG failed to elute at low pH (lane 6). Most IgG remains on beads (lane 9).

    (left) Mouse IgG (anti-Lamin B1 IgG1; 66095-1-Ig, lane 1) was bound to CleanAb rabbit beads (flowthrough in lane 2), then functionalized on beads with NHS-Azide (flowthrough in lane 3) and then with DBCO-Oligo (flowthrough in lane 4). Excess oligo was successfully removed as shown in SYBR Gold DNA staining and the oligo-conjugated IgG was eluted with high recovery at neutral pH (lane 6). Desalting was done with Zeba spin desalting columns (lane 8). Only very little IgG remaining on beads (lane 9). Note: the CleanAb Elution Buffer can interfere with SDS gels, which can make the CleanAb elution appear washed out. (right) Mouse IgG (anti-Lamin B1 IgG1; 66095-1-Ig, lane 1) was bound to Protein A beads (flowthrough in lane 2), Excess oligo was successfully removed as shown in SYBR Gold DNA staining but the oligo-conjugated IgG failed to elute at low pH (lane 6). Most IgG remains on beads (lane 9).

  • Immunostaining of HeLa cells with rabbit anti-CD147 antibodies (11989-1-AP, 1:100, orange hot), chemically conjugated to a 15-nt DNA oligonucleotide and purified using CleanAB beads. Detection was performed by hybridization with an imaging DNA strand labeled with ATTO643. Nuclei were counterstained with DAPI (cyan). Direct comparison of CleanAb product and desalted product demonstrates functionality of both products. While signal intensity is lower for the desalted sample, successful staining can still be achieved.

    Immunostaining of HeLa cells with rabbit anti-CD147 antibodies (11989-1-AP, 1:100, orange hot), chemically conjugated to a 15-nt DNA oligonucleotide and purified using CleanAB beads. Detection was performed by hybridization with an imaging DNA strand labeled with ATTO643. Nuclei were counterstained with DAPI (cyan). Direct comparison of CleanAb product and desalted product demonstrates functionality of both products. While signal intensity is lower for the desalted sample, successful staining can still be achieved.

  • Immunostaining of HeLa cells with rabbit anti-CD147 antibodies (11989-1-AP, 1:100, orange hot), chemically conjugated to a 15-nt DNA oligonucleotide and purified using CleanAB beads. Detection was performed by hybridization with an imaging DNA strand labeled with ATTO643. Nuclei were counterstained with DAPI (cyan). Direct comparison of the two possible CleanAb protocols (post conjugation clean-up and on bead conjugation & clean-up) shows that both approaches are viable and will yield functional antibody-oligo conjugate.

    Immunostaining of HeLa cells with rabbit anti-CD147 antibodies (11989-1-AP, 1:100, orange hot), chemically conjugated to a 15-nt DNA oligonucleotide and purified using CleanAB beads. Detection was performed by hybridization with an imaging DNA strand labeled with ATTO643. Nuclei were counterstained with DAPI (cyan). Direct comparison of the two possible CleanAb protocols (post conjugation clean-up and on bead conjugation & clean-up) shows that both approaches are viable and will yield functional antibody-oligo conjugate.

Conjugation CleanAb Kit for Mouse IgG, Agarose

Conjugation CleanAb Kits for Mouse IgG are designed for fast & easy removal of excess oligos from oligo-conjugated mouse antibodies post conjugation or after on-bead conjugation. The Kit uses coated agarose beads optimized for elution at native pH (pH 7.5), facilitating gentle recovery of your sample from the beads, with high efficiency and excellent recovery rates.
Cat No. CK003

Reactivity

Mouse IgG

Applications

Purification of oligo conjugated IgG

Conjugate

Agarose

Synonyms

Formats:  Mouse IgG-Agarose
规格价格库存

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Product Information

Conjugation CleanAb Kits for Mouse IgG are designed for fast & easy removal of excess oligos from oligo-conjugated mouse antibodies post conjugation or after on-bead conjugation. The Kit uses coated agarose beads optimized for elution at native pH (pH 7.5), facilitating gentle recovery of your sample from the beads, with high efficiency and excellent recovery rates.

DescriptionConjugation CleanAb Kits for Mouse IgG are designed for fast & easy removal of excess oligos from oligo-conjugated mouse antibodies post conjugation or after on-bead conjugation. The Kit uses coated agarose beads optimized for elution at native pH (pH 7.5), facilitating gentle recovery of your sample from the beads, with high efficiency and excellent recovery rates.

• High capacity & high specificity Beads --> Minimized sample loss

• Fast & efficient removal of excess DNA oligo --> No oligo-derived background in end-application

• Elution at native pH 7.5 --> Preserves your conjugate

• High recovery rate of 60 – 80% --> Saves your sample and money

ApplicationsPurification
Binding capacity> 6 mg IgG per 1 ml bead slurry
ConjugateAgarose beads; bead size: ~ 90 µm (cross-linked 4 % agarose beads)
CleanAb Kit Wash Buffer10 mM Tris/Cl pH 7.5, 150 mM NaCl, 0.05 % Nonidet™ P40 Substitute, 0.5 mM EDTA
Bead dilution50% slurry
ClassRecombinant - Animal free production
ImmunogenMouse IgG
RRID/
Storage Buffer20% Ethanol
Storage ConditionShipped at ambient temperature. Upon receipt store at +4°C. Stable for one year. DO not freeze!
ShippingAmbient Temp
Size1 ml
NoteThe beads use a kappa light chain specific binder and will not bind the rare lambda light chain subtype of mouse IgG
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