Six5 (AA 264-294), (Middle Region) antibody

Details for Product No. ABIN954812
Request Want additional data for this product?

The Independent Validation Initiative strives to provide you with high quality data. Find out more

Synonyms Dmahp, MDMAHP, TrexBF, BOR2, DMAHP
AA 264-294, Middle Region
(2), (2), (1), (1), (1), (1)
(13), (9)
Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), ELISA, Western Blotting (WB)
(14), (9), (3), (2), (1)
Pubmed 4 references available
Catalog no. ABIN954812
Quantity 0.4 mL
357.50 $   Plus shipping costs $45.00
Shipping to United States (Change)
Availability Will be delivered in 6 to 8 Business Days

Order hotline:

  • +1 404 474 4654
  • +1 888 205 9894 (TF)
Immunogen KLH conjugated synthetic peptide between 264-294 amino acids from the Central region of Human SIX5. Genename: SIX5
Specificity This antibody recognizes Human SIX5 (Center).
Purification Protein A column, followed by peptide affinity purification
Background The protein encoded by this gene is a homeodomain-containing transcription factor that appears to function in the regulation of organogenesis. This gene is located downstream of the dystrophia myotonica-protein kinase gene. Mutations in this gene are a cause of branchiootorenal syndrome type 2.
Alternate names: DM locus-associated homeodomain protein, DMAHP, Homeobox protein SIX5, Sine oculis homeobox homolog 5
Molecular Weight 74562 Da
Gene ID 147912
NCBI Accession NP_787071
Restrictions For Research Use only
Format Liquid
Concentration 0.25 mg/mL
Buffer PBS containing 0.09% (w/v) Sodium Azide as preservative
Preservative Sodium azide
Handling Advice Avoid repeated freezing and thawing.
Storage 4 °C/-20 °C
Storage Comment Store undiluted at 2-8°C for one month or (in aliquots) at -20°C for longer.
Expiry Date 12 months
Background publications Sato, Nakamura, Cho et al.: "Identification of transcriptional targets for Six5: implication for the pathogenesis of myotonic dystrophy type 1." in: Human molecular genetics, Vol. 11, Issue 9, pp. 1045-58, 2002 (PubMed).

Hoskins, Cramer, Silvius et al.: "Transcription factor SIX5 is mutated in patients with branchio-oto-renal syndrome." in: American journal of human genetics, Vol. 80, Issue 4, pp. 800-4, 2007 (PubMed).

Oguri, Kato, Yokoi et al.: "Assessment of a polymorphism of SDK1 with hypertension in Japanese Individuals." in: American journal of hypertension, Vol. 23, Issue 1, pp. 70-7, 2009 (PubMed).

Yoshida, Kato, Yokoi et al.: "Association of genetic variants with hemorrhagic stroke in Japanese individuals." in: International journal of molecular medicine, Vol. 25, Issue 4, pp. 649-56, 2010 (PubMed).

Hosts (14)
Reactivities (13), (9)
Applications (14), (9), (3), (2), (1)
Epitopes (2), (2), (1), (1), (1), (1)
back to top