MVLSGCAIIVRGQPRGGPPPERQINLSNIRAGNLARRAAATQPDAKDTPDEPWAFPAREFLRKKLIGKEVCFTIENKTPQGREYGMIYLGKDTNGENIAESLVAEGLATRREGMRANNPEQNRLSECEEQAKAAKKGMWSEGNGSHTIRDLKYTIENPRHFVDSHHQKPVNAIIEHVRDGSVVRALLLPDYYLVTVMLSGIKCPTFRREADGSETPEPFAAEAKFFTESRLLQRDVQIILESCHNQNILGTILHPNGNIT

Host

Rabbit

Clonality

Polyclonal

Isotype

IgG

Conjugate

Unconjugated

Purification

Affinity purification.

Molecular Weight

102 kDa

Product Form

Liquid

Formulation

Supplied in Phosphate Buffered Saline, pH 7.3, with 50% Glycerol and 0.02% Sodium Azide.

Storage

Shipped at 4°C. Upon delivery aliquot and store at -20°C. Avoid freeze / thaw cycles.

Synonyms

100 kDa coactivator, EBNA 2 co activator (100kD), EBNA2 coactivator p100, p100, p100 co-activator, p100 coactivator, p100 EBNA2 co activator, SND 1, SND1_HUMAN, Staphylococcal nuclease and tudor domain containing 1, Staphylococcal nuclease domain containing 1, Staphylococcal nuclease domain containing protein 1, Staphylococcal nuclease domain-containing protein 1, TDRD11, TRD 11, TRD11, Tudor domain containing protein 11, Tudor domain-containing protein 11

Isotype Controls

Suitable Secondaries

See all Anti-Rabbit IgG Secondaries →

Disclaimer

This product is for research use only. It is not intended for diagnostic or therapeutic use.

Scientific Validation Data (2)

Enlarge Image

Figure 1: Western Blot - Anti-SND1 Antibody (A87740)

Western blot analysis of extracts of various cell lines, using Anti-SND1 Antibody (A87740) at 1:1,000 dilution. The secondary antibody was Goat Anti-Rabbit IgG H&L Antibody (HRP) at 1:10,000 dilution. Lysates/proteins were present at 25µg per lane. The blocking buffer used was 3% non-fat dry milk in TBST. Detection was with a ECL Basic Kit. Exposure time: 1s.

Enlarge Image

Figure 2: Western Blot - Anti-SND1 Antibody (A87740)

Western blot analysis of extracts from normal (control) and SND1 Rabbit polyclonal antibody knockout (KO) HeLa cells, using Anti-SND1 Antibody (A87740) at 1:1,000 dilution. The secondary antibody was Goat Anti-Rabbit IgG H&L Antibody (HRP) at 1:10,000 dilution. Lysates/proteins were present at 25µg per lane. The blocking buffer used was 3% non-fat dry milk in TBST. Detection was with a ECL Basic Kit. Exposure time: 1s.

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