DiGeorge Syndrome Critical Region Gene 8 (DGCR8) Peptide
DGCR8
Reactivité: Mammifères
Hôte: Synthetic
BP, WB, IHC
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- Antigène Tous les produits DGCR8
- DGCR8 (DiGeorge Syndrome Critical Region Gene 8 (DGCR8))
- Type de proteíne
- Synthetic
- Origine
- Mammifères
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Source
- Synthetic
- Application
- Blocking Peptide (BP), Western Blotting (WB), Immunohistochemistry (IHC)
- Séquence
- DKKDEENELD QEKRVEYAVL DELEDFTDNL ELDEEGAGGF TAKAIVQRDR
- Attributs du produit
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A synthetic peptide for use as a blocking control in assays to test for specificity of DGCR8 antibody,
Alternative Names: DGCR8 control peptide, DGCR8 antibody Blocking Peptide, Anti-DGCR8 Blocking Peptide, Digeorge Syndrome Critical Region Gene 8 Blocking Peptide, C22orf12 Blocking Peptide, DGCRK6 Blocking Peptide, Gy1 Blocking Peptide
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- Indications d'application
- Optimal conditions should be determined by the investigator
- Restrictions
- For Research Use only
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- Format
- Lyophilized
- Reconstitution
- Add 100 µL of distilled water for a final peptide concentration is 1 mg/mL.
- Buffer
- PBS
- Conseil sur la manipulation
- Avoid repeated freeze/thaw cycles.
- Stock
- -20 °C
- Stockage commentaire
- Store at -20 °C long term.
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- Antigène
- DGCR8 (DiGeorge Syndrome Critical Region Gene 8 (DGCR8))
- Synonymes
- MGC78846 Peptide, DGCR8 Peptide, gy1 Peptide, dgcrk6 Peptide, C22orf12 Peptide, DGCRK6 Peptide, Gy1 Peptide, pasha Peptide, D16H22S1742E Peptide, D16H22S788E Peptide, D16Wis2 Peptide, N41 Peptide, Vo59c07 Peptide, si:ch211-106a19.4 Peptide, wu:fc23f08 Peptide, wu:fc38f06 Peptide, DGCR8 microprocessor complex subunit L homeolog Peptide, DiGeorge syndrome critical region gene 8 Peptide, DGCR8 microprocessor complex subunit Peptide, DGCR8, microprocessor complex subunit Peptide, microRNA 3618 Peptide, dgcr8.L Peptide, DGCR8 Peptide, dgcr8 Peptide, Dgcr8 Peptide, MIR3618 Peptide
- Sujet
- DGCR8 contains 2 DRBM (double-stranded RNA-binding) domains and 1 WW domain. It may play a part in the etiology of the velocardiofacial/DiGeorge syndrome (VCFS/DGS), a developmental disorder characterized by structural and functional palate anomalies, conotruncal cardiac malformations, immunodeficiency, hypocalcemia, and typical facial anomalies.
- Poids moléculaire
- 85 kDa
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