ZMYM2 (1250-1300) Rabbit Polyclonal Antibody
CAT#: AP08258PU-N
ZMYM2 (1250-1300) rabbit polyclonal antibody, Aff - Purified
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CNY 5,511.00
货期*
6周
规格
Cited in 1 publication. |
Specifications
Product Data | |
Applications | IHC, WB |
Recommend Dilution | Immunohistochemistry on Paraffin Sections: 10 µg/ml. Western Blot: 0.1 - 1 µg/ml. |
Reactivity | Bovine, Canine, Chicken, Human, Monkey, Mouse, Rat, Orang-Utan |
Host | Rabbit |
Clonality | Polyclonal |
Immunogen | Synthetic peptide corresponding to the amino acids 1250-1300 of human Zinc finger protein 198 |
Specificity | This antibody recognizes Zinc Finger Protein 198 (ZNF198) (ZMYM2) at aa 1250-1300. |
Formulation | PBS containing 0.05% Sodium Azide as preservative and 0.2% Gelatin as stabilizer State: Aff - Purified State: Liquid purified Ig fraction |
Concentration | lot specific |
Purification | Immunoaffinity Chromatography |
Conjugation | Unconjugated |
Storage Condition | Store the antibody undiluted at 2-8°C for one month or (in aliquots) at -20°C for longer. Avoid repeated freezing and thawing. |
Gene Name | zinc finger MYM-type containing 2 |
Database Link | |
Background | Zfp198 (zinc finger protein 198, also known as ZNF198 or Zinc finger MYM-type protein 2) is a transcription factor that contains 9 MYM-type zinc fingers. Zfp198 interacts with, and is modified by, SUMO1 and colocalises with PML to nuclear bodies. Zfp198 has also been shown to stabilise the LSD1-CoREST-HDAC1 complex on chromatin through its MYM-type zinc fingers. A chromosomal translocation resulting in a Zfp198-FGFR1 fusion is associated with stem cell leukemia lymphoma syndrome (SCLL). SCLL usually presents as a lymphoblastic lymphoma in association with a myeloproliferative disorder. |
Synonyms | ZNF198, FIM, RAMP |
Reference Data |
Citations (1)
The use of this Antibodies has been cited in the following citations: |
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Mutations of the Transcriptional Corepressor ZMYM2 Cause Syndromic Urinary Tract Malformations
,Connaughton, DM;Dai, R;Owen, DJ;Marquez, J;Mann, N;Graham-Paquin, AL;Nakayama, M;Coyaud, E;Laurent, EMN;St-Germain, JR;Blok, LS;Vino, A;Klämbt, V;Deutsch, K;Wu, CW;Kolvenbach, CM;Kause, F;Ottlewski, I;Schneider, R;Kitzler, TM;Majmundar, AJ;Buerger, F;Onuchic-Whitford, AC;Youying, M;Kolb, A;Salmanullah, D;Chen, E;van der Ven, AT;Rao, J;Ityel, H;Seltzsam, S;Rieke, JM;Chen, J;Vivante, A;Hwang, DY;Kohl, S;Dworschak, GC;Hermle, T;Alders, M;Bartolomaeus, T;Bauer, SB;Baum, MA;Brilstra, EH;Challman, TD;Zyskind, J;Costin, CE;Dipple, KM;Duijkers, FA;Ferguson, M;Fitzpatrick, DR;Fick, R;Glass, IA;Hulick, PJ;Kline, AD;Krey, I;Kumar, S;Lu, W;Marco, EJ;Wentzensen, IM;Mefford, HC;Platzer, K;Povolotskaya, IS;Savatt, JM;Shcherbakova, NV;Senguttuvan, P;Squire, AE;Stein, DR;Thiffault, I;Voinova, VY;Somers, MJG;Ferguson, MA;Traum, AZ;Daouk, GH;Daga, A;Rodig, NM;Terhal, PA;van Binsbergen, E;Eid, LA;Tasic, V;Rasouly, HM;Lim, TY;Ahram, DF;Gharavi, AG;Reutter, HM;Rehm, HL;MacArthur, DG;Lek, M;Laricchia, KM;Lifton, RP;Xu, H;Mane, SM;Sanna-Cherchi, S;Sharrocks, AD;Raught, B;Fisher, SE;Bouchard, M;Khokha, MK;Shril, S;Hildebrandt, F;,
Am. J. Hum. Genet.
,PubMed ID 32891193
[ZMYM2]
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