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Anticorps
Numéro de catalogue:
(USBI037577-PE)
Fournisseur:
US Biological
Description:
Anti-PPP1R21 Rabbit Polyclonal Antibody (PE (Phycoerythrin))
UOM:
1 * 200 µl
Numéro de catalogue:
(USBI037577-AP)
Fournisseur:
US Biological
Description:
Anti-PPP1R21 Rabbit Polyclonal Antibody (AP (Alkaline Phosphatase))
UOM:
1 * 200 µl
Numéro de catalogue:
(USBI037578-HRP)
Fournisseur:
US Biological
Description:
Anti-KLRC1 Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))
UOM:
1 * 200 µl
Numéro de catalogue:
(USBI043347-FITC)
Fournisseur:
US Biological
Description:
Anti-TSC2 Rabbit Polyclonal Antibody (FITC (Fluorescein Isothiocyanate))
UOM:
1 * 200 µl
Numéro de catalogue:
(USBI037578-AP)
Fournisseur:
US Biological
Description:
Anti-KLRC1 Rabbit Polyclonal Antibody (AP (Alkaline Phosphatase))
UOM:
1 * 200 µl
Fournisseur:
Biotium
Description:
The epitope of this MAb maps in the C-terminus of PTH, a hormone produced by the parathyroid gland that regulates the concentration of calcium and phosphorus in extracellular fluid. This hormone elevates blood Ca2 levels by dissolving the salts in bone and preventing their renal excretion.It is produced in the parathyroid gland as an 84 amino acid single chain polypeptide. It can also be secreted as N-terminal truncated fragments or C-terminal fragments after intracellular degradation, as in case of hypercalcemia. Defects in this gene are a cause of familial isolated hypoparathyroidism (FIH); also called autosomal dominant hypoparathyroidism or autosomal dominant hypocalcemia. FIH is characterized by hypocalcemia and hyperphosphatemia due to inadequate secretion of parathyroid hormone. Symptoms are seizures, tetany and cramps. FIH exist both as autosomal dominant and recessive forms of hypoparathyroidism.
Numéro de catalogue:
(USBIC2262-02E)
Fournisseur:
US Biological
Description:
Anti-ITGAL Mouse Monoclonal Antibody (FITC (Fluorescein)) [clone: 7H117]
UOM:
1 * 1 EA
Numéro de catalogue:
(USBIC2261-48K)
Fournisseur:
US Biological
Description:
Anti-MME Mouse Monoclonal Antibody [clone: HI10a]
UOM:
1 * 1 EA
Numéro de catalogue:
(USBIC2262-02A)
Fournisseur:
US Biological
Description:
Anti-ITGAL Goat Polyclonal Antibody
UOM:
1 * 1 EA
Numéro de catalogue:
(USBIC2262-02D)
Fournisseur:
US Biological
Description:
Anti-ITGAL Mouse Monoclonal Antibody (Biotin) [clone: 7H117]
UOM:
1 * 1 EA
Numéro de catalogue:
(BOSSBS-15454R)
Fournisseur:
Bioss
Description:
Anti-HENMT1 Rabbit Polyclonal Antibody
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-13743R)
Fournisseur:
Bioss
Description:
The catenins are ubiquitously expressed, cytoplasmic proteins that associate with E-cadherin at cellular junctions. Catenin/cadherin complexes play an important role in mediating cellular adhesion. alpha T-catenin, also referred to as VR22, is a 895-amino acid protein that is most abundantally expressed in cardiomyocytes and in the peritubular myoid cells of the testis. alpha T-catenin binds to alpha E-catenin as well as to beta-catenin, and it functions to inhibit Wnt signaling. CTNNA3, the gene that encodes for alpha-T-catenin, is located on chromosome 10, and mutations in this gene show a strong correlation to late-onset Alzheimer's disease (LOAD) as well as to dilated cardiomyopathy.
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-13735R)
Fournisseur:
Bioss
Description:
SHROOM1 is an 852 amino acid protein that contains one ASD1 domain and one ASD2 domain. Localized to both the cytoplasm and the cytoskeleton, SHROOM1 interacts with Actin and is thought to be involved in microtubule assembly during cell elongation, possibly playing a role in the development of the nervous system. Multiple isoforms of SHROOM1 exist due to alternative splicing events. The gene encoding SHROOM1 maps to human chromosome 5, which contains 181 million base pairs and comprises nearly 6% of the human genome. Deletion of the p arm of chromosome 5 leads to Cri du chat syndrome, while deletion of the q arm or of chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome.
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-13744R)
Fournisseur:
Bioss
Description:
Desmoglein proteins are cadherin-type cell adhesion molecules. Desmoglein 4 (dsg4) shares 41% identity with human desmoglein 1, 37% with human desmoglein 2 and 50% with human desmoglein 3. A type I membrane protein of the cadherin protein family, dsg4 is expressed in salivary gland, suprabasal epidermis, hair follicle, testis, prostate and skin. In the hair follicle, dsg4 is an important mediator of keratinocyte cell adhesion and coordinates the transition from proliferation to differentiation. The human DSG4 gene is composed of 16 exons spanning approximately 37 kb of 18q12 and is situated between DSG1 and DSG3.
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-13739R)
Fournisseur:
Bioss
Description:
The claudin superfamily consists of many structurally related proteins in humans. These proteins are important structural and functional components of tight junctions in paracellular transport. Claudins are located in both epithelial and endothelial cells in all tight junction-bearing tissues. Three classes of proteins are known to localize to tight junctions, including the claudins, Occludin and junction adhesion molecules. Claudins, which consist of four transmembrane domains and two extracellular loops, make up tight junction strands. Claudin expression is often highly restricted to specfic regions of different tissues and may have an important role in transcellular transport through tight junctions. Claudin-10 is a 228 amino acid multi-pass membrane protein that belongs to the claudin family and plays an important role in cell-adhesion activity and tight junction-specific events.
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-15449R)
Fournisseur:
Bioss
Description:
Anti-HEG1 Rabbit Polyclonal Antibody
UOM:
1 * 100 µl
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