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chromatography+columns+HyClone+products+(Cytiva)
Catalog Number:
(89297-418)
Supplier:
Genetex
Description:
Goat polyclonal antibody to Quaking / QKI
Catalog Number:
(89296-138)
Supplier:
Genetex
Description:
Goat polyclonal antibody to MICS1 / GHITM
Catalog Number:
(89296-480)
Supplier:
Genetex
Description:
Goat polyclonal antibody to CSRP3
Catalog Number:
(89288-254)
Supplier:
Genetex
Description:
Goat polyclonal antibody to ELKS / RAB6IP2
Catalog Number:
(CA200-343-200)
Supplier:
Rockland Immunochemical
Description:
Primary Mouse Anti-Glutathione-S-Transferase (GST) Reacts with Pan
Catalog Number:
(76108-384)
Supplier:
Bioss
Description:
The X and Y chromosomes are the human sex chromosomes. Chromosome X consists of about 153 million base pairs and nearly 1,000 genes. The combination of an X and Y chromosome lead to normal male development while two copies of X lead to normal female development. There are a number of conditions related to an unsual number and combination of sex chromosomes being inherited. More than one copy of the X chromosome with a Y chromosome causes Klinefelter's syndrome. A single copy of X alone leads to Turner's syndrome. More than 2 copies of the X chromosome, in the absence of a Y chromosome, is known as Triple X syndrome. Color blindness, hemophilia, and Duchenne muscular dystrophy are well known X chromosome-linked conditions which affect males more frequently as males carry a single X chromosome. The FAM104B gene product has been provisionally designated FAM104B pending further characterization.
Catalog Number:
(76108-238)
Supplier:
Bioss
Description:
Chromosome 22 contains over 500 genes and about 49 million bases. Being the second smallest human chromosome, 22 contains a surprising variety of interesting genes. Phelan-McDermid syndrome, Neurofibromatosis type 2 and autism are associated with chromosome 22. A schizophrenia susceptibility locus has been identified on chromosome 22 and studies show that 22q11 deletion symptoms include a high incidence of schizophrenia. Translocations between chromosomes 9 and 22 may lead to the formation of the Philadelphia Chromosome and the subsequent production of the novel fusion protein, BCR-Abl, a potent cell proliferation activator found in several types of leukemia. CCDC134 (coiled-coil domain containing 134), also known as MGC21013 or FLJ22349, is a 229 amino acid protein encoded by a gene mapping to human chromosome 22.
Catalog Number:
(89274-468)
Supplier:
Genetex
Description:
Mouse monoclonal antibody [1B10] to ATP5B
Catalog Number:
(89296-526)
Supplier:
Genetex
Description:
Goat polyclonal antibody to COL4A3BP (aa396-411)
Catalog Number:
(89274-282)
Supplier:
Genetex
Description:
Mouse monoclonal antibody [2F4] to C17orf28
Catalog Number:
(89304-092)
Supplier:
Genetex
Description:
Rabbit Polyclonal antibody to STAT1 (Phospho Tyr701)
Catalog Number:
(89294-290)
Supplier:
Genetex
Description:
Goat polyclonal antibody to DAPP1
Supplier:
New England Biolabs (NEB)
Description:
Peptide-N-Glycosidase F, also known as PNGase F, is an amidase which cleaves between the innermost GlcNAc and asparagine residues of high mannose, hybrid and complex oligosaccharides from N-linked glycoproteins
Catalog Number:
(89295-928)
Supplier:
Genetex
Description:
Goat polyclonal antibody to NDUFS7
Catalog Number:
(75789-384)
Supplier:
Prosci
Description:
SLAM Family Member 6 (SLAMF6) is a 60 kD single-pass type I membrane protein that belongs to the SLAM subgroup of the CD2 family. Human SLAMF6/ NTB-A contains a 205 amino acid extracellular domain (ECD) with one Ig-like V-set and one Ig-like C2-set domain, a 21 amino acid transmembrane segment and an 84 amino acid cytoplasmic domain, with two immunoreceptor tyrosine-based switch motifs. SLAMF6 is a homodimer. SLAMF6 can interact with PTN6 and, upon phosphorylation, with PTN11 and SH2D1A/SAP. Phosphorylation-dependent NTB-A association with SAP is required for full production of IFN- gamma by NK cells and independent of EAT-2 binding. It Triggers cytolytic activity only in natural killer cells (NK) expressing high surface densities of natural cytotoxicity receptors. On B cells, NTB-A modulates immunoglobulin class switching and the balance between tolerance and autoimmunity.
Catalog Number:
(10666-382)
Supplier:
Bioss
Description:
Made up of nearly 146 million bases, chromosome 8 encodes about 800 genes. Translocation of portions of chromosome 8 with amplifications of the c-Myc gene are found in some leukemias and lymphomas, and typically associated with a poor prognosis. Portions of chromosome 8 have been linked to schizophrenia and bipolar disorder. Trisomy 8, also known as Warkany syndrome 2, most often results in early miscarriage but is occasionally seen in a mosaic form in surviving patients who suffer to a varying degree from a number of symptoms including retarded mental and motor development, and certain facial and developmental defects. WRN is a DNA helicase encoded by chromosome 8 and shown defective in those with the early aging disorder Werner syndrome. Chromosome 8 is also associated with Pfeiffer syndrome, congenital hypothyroidism and Waardenburg syndrome. The FAM135B gene product has been provisionally designated FAM135B pending further characterization.
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