1054 Results for: "EMPIGEN\\u00AE+BB+detergent"

Supplier: Abcam

A zwitterionic detergent 1 * 500 mL

Supplier: Thermo Fisher Scientific

Detergent, equivalent to Nonidet P-40. For solubilizing membrane proteins.

Supplier: Diversey

Acidic detergent descaler 1 * 1 Bottle

Supplier: SMEG

This range of professional Smeg washing and thermal disinfection machines are manufactured using high quality materials and components in order to achieve the best results. The wash chambers are 316 L quality stainless steel which is resistant to strong acids (as used in the pharmaceutical and food industries).

Supplier: Abcam

Bile acid detergent 1 * 25 g

Supplier: VWR Chemicals

ADF (Acid detergent fibre) solution for analysing animal feed according a French norm NF V18-122.

Supplier: Abcam

Bile acid detergent 1 * 100 g

Supplier: ProSci Inc.

Complement Factor B (CFB) belongs to the peptidase S1 family of enzymes. It is expressed by hepatocytes and macrophages and localizes to the major histocompatibility complex (MHC) class III region on chromosome 6. CFB which is a component of the alternate pathway of the complement system is cleaved by factor D into 2 fragments: Ba and Bb. Bb. The active subunit Bb is a serine protease which associates with C3b to form the alternative pathway C3 convertase. Bb is involved in the proliferation of preactivated B lymphocytes, while Ba inhibits their proliferation.

Supplier: VWR Chemicals

Non-ionic detergent efficiently hydrophilic proteins from membrane spanning, hydrophobic proteins without altering biological activity.

Supplier: MP Biomedicals

n-Octyl-β-D-Glucopyranoside is a non-ionic detergent for membrane protein.

Supplier: MP Biomedicals

CHAPS is a nondenaturing zwitterionic detergent for solubilizing membrane proteins and breaking protein-protein interactions. Combines the useful properties of both the sulfobetaine-type and the bile salt detergents.

Supplier: G-Biosciences

The Bicinchoninic Acid (BCA) Protein Assay is a highly sensitive colorimetric assay that is compatible with detergent solubilised protein solutions.

Supplier: ProSci Inc.

PDGFRB, a PDGF Receptor type protein kinase, binds only BB PDGF homodimers.

Supplier: VWR Chemicals

High purity Pro-Pure™ grade detergents are carefully packed under inert gas, making them extremely stable.

Supplier: Abcam

A non-ionic detergent 1 * 500 mL

Supplier: Abcam

Zwitterionic detergent used in the solubilization of oleosins. 1 * 1 g

Supplier: VWR Chemicals

Non-ionic detergent efficiently separates hydrophilic proteins from membrane spanning, hydrophobic proteins without altering biological activity.

Supplier: VWR Chemicals

Non ionic detergent efficiently separates hydrophilic proteins from membrane spanning, hydrophobic proteins without altering biological activity.

Supplier: MP Biomedicals

Anionic detergent that may be used in place of SDS for electrophoresis in cold conditions.

Supplier: Abcam

A non-ionic detergent 1 * 100 mL

Supplier: Abcam

A non-ionic detergent 1 * 50 mL

Supplier: VWR Chemicals

Non-ionic detergent efficiently separates hydrophilic proteins from membrane spanning, hydrophobic proteins without altering biological activity.

Supplier: G-Biosciences

Detergent ASB-C8 (4-n-Octylbenzoylamido-propyl-dimethylammonio sulfobetaine). An aminosulfobetaine zwitterionic detergent with a C8 alkyl tail. 1 * 5 g

Supplier: Abcam

BATIMASTAT (BB-94) (DMSO SOLUTION) 1 * 1 mg

Supplier: Bioss

Bardet-Biedl syndrome (BBS) is a pleiotropic genetic disorder characterized by obesity, photoreceptor degeneration, polydactyly, hypogenitalism, renal abnormalities, and developmental delay. Other associated clinical findings in BBS patients include diabetes, hypertension, and congenital heart defects. BBS genes map to multiple loci and encode fourteen proteins, BBS1-BBS14. Many BBS genes encode basal body or cilia proteins, suggesting that BBS is a ciliary dysfunction disorder. BBS10 (Bardet-Biedl syndrome 10), also known as chromosome 12 open reading fame 58, C12orf58 or FLJ23560, is a novel 723 amino acid protein belonging to the TCP-1 chaperonin family. BBS10 localizes to the basal body of primary cilium and assists in protein folding upon ATP hydrolysis. Inhibition of BBS10 has been found to impair ciliogenesis, activate the glycogen synthase kinase 3 pathway and cause peroxisome proliferator-activated receptor nuclear accumulation. The gene encoding BBS10 contains two exons and maps to human chromosome 12q21.2.

Supplier: Bioss

Bardet-Biedl syndrome (BBS) is a pleiotropic genetic disorder characterized by obesity, photoreceptor degeneration, polydactyly, hypogenitalism, renal abnormalities, and developmental delay. Other associated clinical findings in BBS patients include diabetes, hypertension, and congenital heart defects. BBS genes map to multiple loci and encode fourteen proteins, BBS1-BBS14. Many BBS genes encode basal body or cilia proteins, suggesting that BBS is a ciliary dysfunction disorder. BBS10 (Bardet-Biedl syndrome 10), also known as chromosome 12 open reading fame 58, C12orf58 or FLJ23560, is a novel 723 amino acid protein belonging to the TCP-1 chaperonin family. BBS10 localizes to the basal body of primary cilium and assists in protein folding upon ATP hydrolysis. Inhibition of BBS10 has been found to impair ciliogenesis, activate the glycogen synthase kinase 3 pathway and cause peroxisome proliferator-activated receptor nuclear accumulation. The gene encoding BBS10 contains two exons and maps to human chromosome 12q21.2.

Supplier: Bioss

Bardet-Biedl syndrome (BBS) is a pleiotropic genetic disorder characterized by obesity, photoreceptor degeneration, polydactyly, hypogenitalism, renal abnormalities, and developmental delay. Other associated clinical findings in BBS patients include diabetes, hypertension, and congenital heart defects. BBS genes map to multiple loci and encode fourteen proteins, BBS1-BBS14. Many BBS genes encode basal body or cilia proteins, suggesting that BBS is a ciliary dysfunction disorder. BBS10 (Bardet-Biedl syndrome 10), also known as chromosome 12 open reading fame 58, C12orf58 or FLJ23560, is a novel 723 amino acid protein belonging to the TCP-1 chaperonin family. BBS10 localizes to the basal body of primary cilium and assists in protein folding upon ATP hydrolysis. Inhibition of BBS10 has been found to impair ciliogenesis, activate the glycogen synthase kinase 3 pathway and cause peroxisome proliferator-activated receptor nuclear accumulation. The gene encoding BBS10 contains two exons and maps to human chromosome 12q21.2.

Supplier: Diversey

Ready to use detergent disinfectant for the cleaning and disinfection of all surfaces in food premises.

Supplier: Bioss

Bardet-Biedl syndrome (BBS) is a pleiotropic genetic disorder characterized by obesity, photoreceptor degeneration, polydactyly, hypogenitalism, renal abnormalities, and developmental delay. Other associated clinical findings in BBS patients include diabetes, hypertension, and congenital heart defects. BBS genes map to multiple loci and encode fourteen proteins, BBS1-BBS14. Many BBS genes encode basal body or cilia proteins, suggesting that BBS is a ciliary dysfunction disorder. BBS10 (Bardet-Biedl syndrome 10), also known as chromosome 12 open reading fame 58, C12orf58 or FLJ23560, is a novel 723 amino acid protein belonging to the TCP-1 chaperonin family. BBS10 localizes to the basal body of primary cilium and assists in protein folding upon ATP hydrolysis. Inhibition of BBS10 has been found to impair ciliogenesis, activate the glycogen synthase kinase 3 pathway and cause peroxisome proliferator-activated receptor nuclear accumulation. The gene encoding BBS10 contains two exons and maps to human chromosome 12q21.2.

Supplier: Bioss

Bardet-Biedl syndrome (BBS) is a pleiotropic genetic disorder characterized by obesity, photoreceptor degeneration, polydactyly, hypogenitalism, renal abnormalities, and developmental delay. Other associated clinical findings in BBS patients include diabetes, hypertension, and congenital heart defects. BBS genes map to multiple loci and encode fourteen proteins, BBS1-BBS14. Many BBS genes encode basal body or cilia proteins, suggesting that BBS is a ciliary dysfunction disorder. BBS10 (Bardet-Biedl syndrome 10), also known as chromosome 12 open reading fame 58, C12orf58 or FLJ23560, is a novel 723 amino acid protein belonging to the TCP-1 chaperonin family. BBS10 localizes to the basal body of primary cilium and assists in protein folding upon ATP hydrolysis. Inhibition of BBS10 has been found to impair ciliogenesis, activate the glycogen synthase kinase 3 pathway and cause peroxisome proliferator-activated receptor nuclear accumulation. The gene encoding BBS10 contains two exons and maps to human chromosome 12q21.2.