ALX4 Mouse Monoclonal Antibody (Biotin conjugated) [Clone ID: OTI2F2]

CAT#: TA505146AM

ALX4 mouse monoclonal antibody,clone 2F2, Biotinylated

Product Images

HEK293T cells were transfected with the pCMV6-ENTRY control (Left lane) or pCMV6-ENTRY ALX4 (RC224459, 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-ALX4. Positive lysates LY411892 (100ug) and LC411892 (20ug) can be purchased separately from OriGene.

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  HEK293T cells transfected with either RC224459 overexpress plasmid (Red) or empty vector control plasmid (Blue) were immunostained by anti-ALX4 antibody (TA505146), and then analyzed by flow cytometry.

Specifications

Product Data

• Clone Name: OTI2F2
• Applications: FC, WB
• Recommended Dilution: WB 1:1000, FLOW 1:100
• Reactivities: Human, Mouse, Rat
• Host: Mouse
• Isotype: IgG1
• Clonality: Monoclonal
• Immunogen: Full length human recombinant protein of human ALX4(NP_068745) produced in HEK293T cell.
• Formulation: PBS (PH 7.3) containing 1% BSA, 50% glycerol and 0.02% sodium azide.
• Concentration: 0.5 mg/ml
• Purification: Purified from mouse ascites fluids or tissue culture supernatant by affinity chromatography (protein A/G)
• Conjugation: Biotin
• Storage: Store at -20°C as received.
• Stability: Stable for 12 months from date of receipt.
• Predicted Protein Size: 44.1 kDa
• Gene Name: ALX homeobox 4
• Database Link:
  NP_068745
  Entrez Gene 11695 MouseEntrez Gene 296511 RatEntrez Gene 60529 Human
  UniProt ID Q9H161
• Background: This gene encodes a paired-like homeodomain transcription factor expressed in the mesenchyme of developing bones, limbs, hair, teeth, and mammary tissue. Mutations in this gene cause parietal foramina 2 (PFM2); an autosomal dominant disease characterized by deficient ossification of the parietal bones. Mutations in this gene also cause a form of frontonasal dysplasia with alopecia and hypogonadism; suggesting a role for this gene in craniofacial development, mesenchymal-epithelial communication, and hair follicle development. Deletion of a segment of chromosome 11 containing this gene, del(11)(p11p12), causes Potocki-Shaffer syndrome (PSS); a syndrome characterized by craniofacial anomalies, mental retardation, multiple exostoses, and genital abnormalities in males. In mouse, this gene has been shown to use dual translation initiation sites located 16 codons apart. [provided by RefSeq]
• Synonyms: CRS5; FND2

Reference Data

• Protein Families: Druggable Genome