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Image Unavailable-BOSSBS-11687R-A680

Anti-PROSAAS Rabbit Polyclonal Antibody (Alexa Fluor® 680)

Catalog Number: (BOSSBS-11687R-A680)
Supplier: Bioss
Description: PCSK1N is a 260 amino acid protein that is both secreted and localised to the trans-Golgi network. Expressed in pancreas and brain, PCSK1N is thought to play a role in the control of the neuroendocrine secretory pathway and may also be involved in PCSK1 inhibition. The gene encoding PCSK1N maps to human chromosome X, which contains nearly 153 million base pairs and houses over 1000 genes. In conjunction with chromosome Y, chromosome X is responsible for sex determination, as an X and a Y chromosome lead to normal male development, while two copies of an X chromosome lead to normal female development. There are a number of conditions related to an abnormal number and combination of sex chromosomes, some of which include Turner's syndrome, color blindness, hemophilia and Duchenne muscular dystrophy.
UOM: 1 * 100 µl
Image Unavailable-APOSOR11310-1G

4-Hydroxy-3-methoxycinnamic acid (Ferulic acid) 99%

Supplier: Apollo Scientific
Description: 4-Hydroxy-3-methoxycinnamic acid (Ferulic acid) 99%

Image Unavailable-APOSPC49811-250MG

2-Bromo-4-chloro-5-fluorobenzoic acid 95%

Supplier: Apollo Scientific
Description: 2-Bromo-4-chloro-5-fluorobenzoic acid 95%

Image Unavailable-APOSOR318079-1G

1,6-Naphthyridine-5-carboxylic acid 95+%

Catalog Number: (APOSOR318079-1G)
Supplier: Apollo Scientific
Description: 1,6-Naphthyridine-5-carboxylic acid 95+%
UOM: 1 * 1 g
Image Unavailable-H26877.03

3,6-Dimethoxypyridazine-4-carboxylic acid 96%

Catalog Number: (H26877.03)
Supplier: Thermo Fisher Scientific
Description: 3,6-Dimethoxypyridazine-4-carboxylic acid 96%
UOM: 1 * 1 g

MSDS Certificates


Image Unavailable-A19194.22

3-Methyl-2-thenoic acid ≥98%

Supplier: Thermo Fisher Scientific
Description: 3-Methyl-2-thenoic acid ≥98%

MSDS Certificates

Image Unavailable-B25450.06

(±)-Indoline-2-carboxylic acid 95%

Supplier: Thermo Fisher Scientific
Description: (±)-Indoline-2-carboxylic acid 95%

MSDS Certificates

Image Unavailable-APOSBIPG1113-100MG

Azido-PEG24-acid

Supplier: Apollo Scientific
Description: Azido-PEG24-acid

Image Unavailable-APOSOR909248-5G

1-(4-Bromophenyl)cyclopentanecarboxylic acid 97%

Catalog Number: (APOSOR909248-5G)
Supplier: Apollo Scientific
Description: 1-(4-Bromophenyl)cyclopentanecarboxylic acid 97%
UOM: 1 * 5 g
Image Unavailable-BNC040638-100

Anti-FGF23 Mouse Monoclonal Antibody (CF405S) [clone: FGF23/638]

Supplier: Biotium
Description: Fibroblast growth factor-1 (FGF-1), also designated acidic FGF, and fibroblast growth factor-2 (FGF-2), also designated basic FGF, are members of a family of growth factors that stimulate proliferation of cells of mesenchymal, epithelial and neuroectodermal origin. Additional members of the FGF family include the oncogenes FGF-3 (Int2) and FGF-4 (hst/Kaposi), FGF-5, FGF-6, FGF-7 (KGF), FGF-8 (AIGF), FGF-9 (GAF) and FGF-10 through FGF-23. Members of the FGF family share 30-55% amino acid sequence identity and similar gene structure, and are capable of transforming cultured cells when overexpressed in trans- fected cells. Cellular receptors for FGFs are members of a second multigene family, including four tyrosine kinases designated Flg (FGFR-1), Bek (FGFR-L), TKF and FGFR-3.

Image Unavailable-BOSSBS-8333R-A488

Anti-RDH13 Rabbit Polyclonal Antibody (Alexa Fluor® 488)

Catalog Number: (BOSSBS-8333R-A488)
Supplier: Bioss
Description: RDH13, also known as all-trans and 9-cis retinol dehydrogenase 13 or SDR7C3, is a 331 amino acid mitochondrial protein belonging to the short-chain dehydrogenases/reductases (SDR) family. Widely expressed, mostly in eye, pancreas, placenta and lung, RDH13 localizes on the outer side of the inner mitochondrial membrane. Related to microsomal retinoid oxidoreductase RDH11, RDH13 is considered to be a major enzyme among the RDH family of proteins. Catalytically active, RDH13 recognizes retinoids as substrates and may function in retinoic acid production. RDH13 may function to protect the mitochondria against oxidative stress. Leber congenital amaurosis (LCA) type 3, an inherited autosomal recessive retinal disease, has been associated with defects of RDH13. LCA represents the most common genetic cause of congenital visual impairment in infants and children.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-11785R-A647

Anti-SPG21 Rabbit Polyclonal Antibody (Alexa Fluor® 647)

Catalog Number: (BOSSBS-11785R-A647)
Supplier: Bioss
Description: Maspardin is a 308 amino acid cytoplasmic protein that is widely expressed. Belonging to the AB hydrolase superfamily, Maspardin colocalizes with CD4 on endosomal/trans-Golgi network. It is thought that Maspardin may act as a negative regulatory factor in CD4-dependent T-cell activation. Defects in the gene encoding Maspardin are the result of hereditary spastic paraplegia autosomal recessive type 21 (also designated Mast syndrome), an autosomal recessive neurodegenerative disorder characterized by a slow, gradual, progressive weakness and spasticity of the lower limbs. The gene encoding Maspardin is encoded by human chromosome 15, which houses over 700 genes and comprises nearly 3% of the human genome.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-11785R-CY3

Anti-SPG21 Rabbit Polyclonal Antibody (Cy3®)

Catalog Number: (BOSSBS-11785R-CY3)
Supplier: Bioss
Description: Maspardin is a 308 amino acid cytoplasmic protein that is widely expressed. Belonging to the AB hydrolase superfamily, Maspardin colocalizes with CD4 on endosomal/trans-Golgi network. It is thought that Maspardin may act as a negative regulatory factor in CD4-dependent T-cell activation. Defects in the gene encoding Maspardin are the result of hereditary spastic paraplegia autosomal recessive type 21 (also designated Mast syndrome), an autosomal recessive neurodegenerative disorder characterized by a slow, gradual, progressive weakness and spasticity of the lower limbs. The gene encoding Maspardin is encoded by human chromosome 15, which houses over 700 genes and comprises nearly 3% of the human genome.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-13345R-CY5

Anti-GGA3 Rabbit Polyclonal Antibody (Cy5®)

Catalog Number: (BOSSBS-13345R-CY5)
Supplier: Bioss
Description: The GGA family of proteins (Golgi-localized, g-Adaptin ear-containing, ARF-binding proteins) are ubiquitous coat proteins that facilitate the trafficking of soluble proteins from the trans-Golgi network (TGN) to endosomes/lysosomes by means of interactions with TGN-sorting receptors, ARF (ADP-ribosylation factor), and clathrin. Members of the GGA family, GGA1,GGA2 (also known as VEAR) and GGA3, are multi-domain proteins that bind mannose 6-phosphate receptors (MPRs). GGAs have modular structures with an N-terminal VHS (VPS27, Hrs and STAM) domain followed by a GAT (GGA and Tom1) domain, a connecting hinge segment and a C-terminal GAE (g-Adaptin ear) domain. The amino-terminal VHS domains of GGAs form complexes with the cytoplasmic domains of sorting receptors by recognizing acidic-cluster di-leucine (ACLL) sequences. The human GGA3 gene maps to chromosome 17 and encodes a 723 amino acid protein that shares 46% sequence identity with GGA1 and 38% with GGA2.
UOM: 1 * 100 µl
Image Unavailable-APOSPC3912-5G

2-Fluoro-4-nitrobenzoic acid 97%

Catalog Number: (APOSPC3912-5G)
Supplier: Apollo Scientific
Description: 2-Fluoro-4-nitrobenzoic acid 97%
UOM: 1 * 5 g
Image Unavailable-APOSPC430506-1G

2-Chloro-4-fluoro-5-sulphamoylbenzoic acid

Catalog Number: (APOSPC430506-1G)
Supplier: Apollo Scientific
Description: 2-Chloro-4-fluoro-5-sulphamoylbenzoic acid
UOM: 1 * 1 g
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Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the call is still displayed and you need assistance, please call us on +353 1 88 22222.
This product is marked as restricted and can only be purchased by approved Shipping Accounts. If you need further assistance, email VWR Regulatory Department at eurega_services@eu.vwr.com
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