TSHZ1 Mouse Monoclonal Antibody [Clone ID: OTI8A9]

CAT#: CF809993

Carrier-free (BSA/glycerol-free) TSHZ1 mouse monoclonal antibody,clone OTI8A9

Product Images

HEK293T cells were transfected with the pCMV6-ENTRY control (Left lane) or pCMV6-ENTRY TSHZ1 (RC215916, Right lane) cDNA for 48 hrs and lysed. Equivalent amounts of cell lysates (5 ug per lane) were separated by SDS-PAGE and immunoblotted with anti-TSHZ1 (1:2000). Positive lysates LY417073 (100ug) and LC417073 (20ug) can be purchased separately from OriGene.

Specifications

Product Data

• Clone Name: OTI8A9
• Applications: WB
• Recommended Dilution: WB 1:2000
• Reactivities: Human, Mouse, Rat
• Host: Mouse
• Isotype: IgG1
• Clonality: Monoclonal
• Immunogen: Human recombinant protein fragment corresponding to amino acids 29-176 of human TSHZ1(NP_005777) produced in E.coli.
• Formulation: Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose)
• Reconstitution Method: For reconstitution, we recommend adding 100uL distilled water to a final antibody concentration of about 1 mg/mL. To use this carrier-free antibody for conjugation experiment, we strongly recommend performing another round of desalting process. (OriGene recommends Zeba Spin Desalting Columns, 7KMWCO from Thermo Scientific)
• Purification: Purified from mouse ascites fluids or tissue culture supernatant by affinity chromatography (protein A/G)
• Conjugation: Unconjugated
• Storage: Store at -20°C as received.
• Stability: Stable for 12 months from date of receipt.
• Predicted Protein Size: 112.5 kDa
• Gene Name: Homo sapiens teashirt zinc finger homeobox 1 (TSHZ1), transcript variant 2, mRNA.
• Database Link:
  NP_005777
  Entrez Gene 110796 MouseEntrez Gene 307217 RatEntrez Gene 10194 Human
  UniProt ID Q6ZSZ6
• Background: This gene encodes a colon cancer antigen that was defined by serological analysis of recombinant cDNA expression libraries. The encoded protein is a member of the teashirt C2H2-type zinc-finger protein family and may be involved in transcriptional regulation of developmental processes. Mutations in this gene may be associated with congenital aural atresia syndrome. [provided by RefSeq, Jan 2012]
• Synonyms: CAA; NY-CO-33; SDCCAG33; TSH1

Reference Data

• Protein Families: Transcription Factors