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chromatography+columns+HyClone+products+(Cytiva)
Catalog Number:
(89323-864)
Supplier:
Genetex
Description:
Purity: Purified by antigen-affinity chromatography. Species Reactivity: Human, Mouse Tested Applications: WB Pkg Size: 100 ul
Catalog Number:
(89323-874)
Supplier:
Genetex
Description:
Purity: Purified by antigen-affinity chromatography. Species Reactivity: Human Tested Applications: IHC-P, WB Pkg Size: 100 ul
Catalog Number:
(89319-318)
Supplier:
Genetex
Description:
Rabbit Polyclonal antibody to CYP26A1 (cytochrome P450, family 26, subfamily A, polypeptide 1)
Catalog Number:
(89348-568)
Supplier:
Genetex
Description:
Rabbit Polyclonal antibody to c-Yes (v-yes-1 Yamaguchi sarcoma viral oncogene homolog 1)
Catalog Number:
(89354-888)
Supplier:
Genetex
Description:
Rabbit Polyclonal antibody to ASB9 (ankyrin repeat and SOCS box-containing 9)
Catalog Number:
(89319-036)
Supplier:
Genetex
Description:
Rabbit Polyclonal antibody to HSF2BP (heat shock transcription factor 2 binding protein)
Catalog Number:
(89356-556)
Supplier:
Genetex
Description:
Rabbit Polyclonal antibody to PAK1 (p21 protein (Cdc42/Rac)-activated kinase 1)
Catalog Number:
(89319-784)
Supplier:
Genetex
Description:
Rabbit Polyclonal antibody to APE1 (DNA-(apurinic or apyrimidinic site) lyase)
Catalog Number:
(89356-920)
Supplier:
Genetex
Description:
Rabbit Polyclonal antibody to PIG3 (tumor protein p53 inducible protein 3)
Catalog Number:
(89319-488)
Supplier:
Genetex
Description:
Rabbit Polyclonal antibody to GIT1 (G protein-coupled receptor kinase interacting ArfGAP 1)
Catalog Number:
(89349-894)
Supplier:
Genetex
Description:
Rabbit Polyclonal antibody to PAI2 (serpin peptidase inhibitor, clade B (ovalbumin), member 2)
Supplier:
TCI America
Description:
[Reagent for Ion-Pair Chromatography]
CAS Number: 22767-50-6 MDL Number: MFCD00007543 Molecular Formula: C7H16O3S Molecular Weight: 202.24 Purity/Analysis Method: >98.0% (T) Form: Crystal Melting point (°C): 300
Supplier:
Remco Products
Description:
Reusable and washable, the one-piece construction increases the gown's hygiene and durability.
Catalog Number:
(10340-052)
Supplier:
Bioss
Description:
TNFRSF14 is a type I membrane protein belonging to the TNF receptor superfamily. This receptor mediates herpes virus entry into cells during infection. TNFRSF14 is able to inhibit the proliferation, activation, and cytokine production of T cells. It has an extracellular domain containing several cysteine-rich repeats and a short cytoplasmic region containing a TRAF (TNF receptor-associated factor) interaction domain. The extracellular domain of TNFRSF14 interacts with the herpes simplex virus envelope glycoprotein D. TNFRSF14 binds two cellular ligands: lymphotoxin alpha and LIGHT. LIGHT is a transmembrane protein expressed and shed from the surface of activated T cells, exhibits inducible expression, and competes with HSV glycoprotein D for HVEM, a receptor expressed by T lymphocytes. The LIGHT:TNFRSF14 interaction controls immune response functions by cell death induction as well as cell activation. TNFRSF14 is expressed by peripheral blood T cells, B cells, monocytes and in various tissues enriched in lymphoid cells.
Catalog Number:
(10487-222)
Supplier:
Bioss
Description:
ODF3B, also known as ODF3L3 (outer dense fiber protein 3-like protein 3), is a 253 amino acid protein belonging to the ODF3 family. Existing as two isoforms produced by alternative splicing, ODF3B contains one DUF1309 repeat. The gene that encodes ODF3B maps to human chromosome 22, which 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.
Catalog Number:
(10482-790)
Supplier:
Bioss
Description:
Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma.
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