Oligonucleotides
Biotium SOX9 / SRY-box 9(SOX9/2287R), CF740 conjugate, 0.1mg/mL
The specificity of this monoclonal antibody to its intended target was validated by HuProt™ Array, containing more than 19, 000, full-length human proteins. Plays an important role in the normal skeletal development. May regulate the expression of other genes involved in chondrogenesis by acting as a transcription factor for these genes. Nucleus (Potential). Campomelic dysplasia (CMD1) : Rare, often lethal, dominantly inherited, congenital osteo-chondrodysplasia, associated with male-to-female autosomal sex reversal in two-thirds of the affected karyotypic males. A disease of the newborn characterized by congenital bowing and angulation of long bones, unusually small scapulae, deformed pelvis and spine and a missing pair of ribs. Craniofacial defects such as cleft palate, micrognathia, flat face and hypertelorism are common. Primary antibodies are available purified, or with a selection of fluorescent CF Dyes and other labels. CF Dyes offer exceptional brightness and phot
Biotium SOX9 / SRY-box 9(rSOX9/2288), CF405S conjugate, 0.1mg/mL
The specificity of this monoclonal antibody to its intended target was validated by HuProt™ Array, containing more than 19, 000, full-length human proteins. Plays an important role in the normal skeletal development. May regulate the expression of other genes involved in chondrogenesis by acting as a transcription factor for these genes. Nucleus (Potential). Campomelic dysplasia (CMD1) : Rare, often lethal, dominantly inherited, congenital osteo-chondrodysplasia, associated with male-to-female autosomal sex reversal in two-thirds of the affected karyotypic males. A disease of the newborn characterized by congenital bowing and angulation of long bones, unusually small scapulae, deformed pelvis and spine and a missing pair of ribs. Craniofacial defects such as cleft palate, micrognathia, flat face and hypertelorism are common. Primary antibodies are available purified, or with a selection of fluorescent CF Dyes and other labels. CF Dyes offer exceptional brightness and phot
Sino Biological Recombinant Human GAPDH Protein (His Tag)
A DNA sequence encoding the human GAPDH (P04406) (Met 1-Glu 335) was expressed, with a polyhistidine tag at the N-terminus.
CPC Scientific 5FAM-Gly-Gly-Gly-Pro-Ala-Thr(PO3H2)-Pro-Lys-Lys-Ala-Lys-Lys-Leu-OH (trifluoroacetate salt) 1MG
ONE-LETTER SEQUENCE: 5FAM-GGGPA-Thr(PO3H2)-PKKAKKLMOLECULAR FORMULA: C77H112N17O24P1MOLECULAR WEIGHT:1690.8STORAGE CONDITIONS: -20 5CRESEARCH AREA: Protein Kinases and Phosphatases
Medchemexpress LLC Odn 1826 | 202668-42-6 | 10MG
ODN 1826 is a class B CpG oligodeoxynucleotide that functions as a mouse TLR9 agonist. It is a synthetic, single-stranded 20-mer with a full phosphorothioate backbone and unmethylated CpG motifs, used to activate B cells and induce pro-inflammatory cytokines in preclinical mouse studies.
- Synthetic 20-mer oligodeoxynucleotide with a phosphorothioate backbone
- Contains unmethylated CpG motifs that activate mouse TLR9
- Potent stimulator of B cells and pro-inflammatory cytokine production
- Commonly used as a vaccine adjuvant or immunostimulant in mouse models
- Nuclease resistant for improved in vivo stability
- High purity (>98% HPLC) available and lot-tested for biological activity
CPC Scientific 5FAM-Leu-Lys-Lys-Leu-Thr-Arg-Arg-Ala-Ser-Phe-Ser-Gly-Gln-OH (trifluoroacetate salt) 1MG
ONE-LETTER SEQUENCE: 5FAM-LKKLTRRASFSGQMOLECULAR FORMULA: C86H124N22O24MOLECULAR WEIGHT:1850.1STORAGE CONDITIONS: -20 5CRESEARCH AREA: Protein Kinases and Phosphatases