Sie suchten nach: L(+)-Asparagins\u00E4ure

Artikel-Nr: (MOLE22164347-1KG)

Lieferant: Molekula

Hersteller Artikel Nummer : 22164347-1KG

Beschreibung: (±)-Asparaginsäure

UOM: 1 * 1 kg

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Artikel-Nr: (EHERC10304950)

Lieferant: EHRENSTORFER

Hersteller Artikel Nummer : C10304950

Beschreibung: (±)-Asparaginsäure

UOM: 1 * 0,1 g

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Artikel-Nr: (PRSI55-859)

Lieferant: ProSci Inc.

Hersteller Artikel Nummer : 55-859

Beschreibung: The protein encoded by this gene is a membrane-bound arginine/lysine carboxypeptidase. Its expression is associated with monocyte to macrophage differentiation. This encoded protein contains hydrophobic regions at the amino and carboxy termini and has 6 potential asparagine-linked glycosylation sites. The active site residues of carboxypeptidases A and B are conserved in this protein. Three alternatively spliced transcript variants encoding the same protein have been described for this gene. [provided by RefSeq].

UOM: 1 * 400 µl

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Lieferant: BACHEM BIOCHEMICA

Beschreibung: L(+)-Asparaginsäure

Artikel-Nr: (PRSI55-532)

Lieferant: ProSci Inc.

Hersteller Artikel Nummer : 55-532

Beschreibung: This gene encodes a protein which is a member of family 38 of the glycosyl hydrolases. The protein is located in the Golgi and catalyzes the final hydrolytic step in the asparagine-linked oligosaccharide (N-glycan) maturation pathway. Mutations in the mouse homolog of this gene have been shown to cause a systemic autoimmune disease similar to human systemic lupus erythematosus.

UOM: 1 * 400 µl

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Artikel-Nr: (PRSI33-605)

Lieferant: ProSci Inc.

Hersteller Artikel Nummer : 33-605

Beschreibung: ASRGL1 (Asparaginase-like protein 1), also known as CRASH, belongs to the Ntn-hydrolase family. Asparaginases utilize asparagine as a substrate to produce aspartic acid and ammonia. ASRGL1 has been identified as a autoantigenic protein that is present in the mid-piece of sperm after obstruction of the male reproductive tract. It is expressed highly in testis, but is also expressed in brain, kidney and gastrointestinal tissues. High levels of ASRGL1 have also been identified in ovarian, uterine and mammary tumors in comparison with normal tissues of the same origin.

UOM: 1 * 100 µG

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Artikel-Nr: (PRSI30-207)

Lieferant: ProSci Inc.

Hersteller Artikel Nummer : 30-207

Beschreibung: DDOST is a component of the oligosaccharyltransferase complex which catalyzes the transfer of high-mannose oligosaccharides to asparagine residues on nascent polypeptides in the lumen of the rough endoplasmic reticulum. The protein complex co-purifies with ribosomes. DDOST is also implicated in the processing of advanced glycation endproducts (AGEs), which form from non-enzymatic reactions between sugars and proteins or lipids and are associated with aging and hyperglycemia.

UOM: 1 * 100 µG

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Artikel-Nr: (PRSI29-723)

Lieferant: ProSci Inc.

Hersteller Artikel Nummer : 29-723

Beschreibung: SLC1A5 has a broad substrate specificity, a preference for zwitterionic amino acids, and a sodium-dependence. It accepts as substrates all neutral amino acids, including glutamine, asparagine, and branched-chain and aromatic amino acids, and excludes methylated amino acids, anionic amino acids, and cationic amino acids. It acts as a cell surface receptor for feline endogenous virus RD114, baboon M7 endogenous virus and type D simian retroviruses.

UOM: 1 * 100 µG

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Artikel-Nr: (PRSI56-642)

Lieferant: ProSci Inc.

Hersteller Artikel Nummer : 56-642

Beschreibung: This gene is thought to play an important role in calcium homeostasis. The gene is expressed from two promoters and undergoes extensive alternative splicing. The encoded set of proteins share varying amounts of overlap near their N-termini but have substantial variations in their C-terminal domains resulting in distinct functional properties. The longest isoforms (a and f) include a C-terminal Aspartyl/Asparaginyl beta-hydroxylase domain that hydroxylates aspartic acid or asparagine residues in the epidermal growth factor (EGF)-like domains of some proteins, including protein C, coagulation factors VII, IX, and X, and the complement factors C1R and C1S. Other isoforms differ primarily in the C-terminal sequence and lack the hydroxylase domain, and some have been localized to the endoplasmic and sarcoplasmic reticulum. Some of these isoforms are found in complexes with calsequestrin, triadin, and the ryanodine receptor, and have been shown to regulate calcium release from the sarcoplasmic reticulum. Some isoforms have been implicated in metastasis.

UOM: 1 * 400 µl

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Artikel-Nr: (PRSI26-032)

Lieferant: ProSci Inc.

Hersteller Artikel Nummer : 26-032

Beschreibung: Cytochrome c oxidase (COX), the terminal component of the mitochondrial respiratory chain, catalyzes the electron transfer from reduced cytochrome c to oxygen. COX10 is heme A: farnesyltransferase, which is not a structural subunit but required for the expression of functional COX and functions in the maturation of the heme A prosthetic group of COX. This protein is predicted to contain 7-9 transmembrane domains localized in the mitochondrial inner membrane. A gene mutation, which results in the substitution of a lysine for an asparagine (N204K), is identified to be responsible for cytochrome c oxidase deficiency. In addition, this gene is disrupted in patients with CMT1A (Charcot-Marie-Tooth type 1A) duplication and with HNPP (hereditary neuropathy with liability to pressure palsies) deletion.Cytochrome c oxidase (COX), the terminal component of the mitochondrial respiratory chain, catalyzes the electron transfer from reduced cytochrome c to oxygen. This component is a heteromeric complex consisting of 3 catalytic subunits encoded by mitochondrial genes and multiple structural subunits encoded by nuclear genes. The mitochondrially-encoded subunits function in electron transfer, and the nuclear-encoded subunits may function in the regulation and assembly of the complex. This nuclear gene encodes heme A:farnesyltransferase, which is not a structural subunit but required for the expression of functional COX and functions in the maturation of the heme A prosthetic group of COX. This protein is predicted to contain 7-9 transmembrane domains localized in the mitochondrial inner membrane. A gene mutation, which results in the substitution of a lysine for an asparagine (N204K), is identified to be responsible for cytochrome c oxidase deficiency. In addition, this gene is disrupted in patients with CMT1A (Charcot-Marie-Tooth type 1A) duplication and with HNPP (hereditary neuropathy with liability to pressure palsies) deletion. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.

UOM: 1 * 50 µG

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Lieferant: MP Biomedicals

Beschreibung: DL-Aspartic acid (DL-Asp) is a racemic mixture of the proteinogenic amino acid L-aspartate and the non-proteinogenic amino acid D-aspartate. DL-Aspartic acid is used in studies on factors and conditions that enhance semen and sperm quality.

Artikel-Nr: (PRSI55-363)

Lieferant: ProSci Inc.

Hersteller Artikel Nummer : 55-363

Beschreibung: Cytochrome c oxidase (COX), the terminal component of the mitochondrial respiratory chain, catalyzes the electron transfer from reduced cytochrome c to oxygen. This component is a heteromeric complex consisting of 3 catalytic subunits encoded by mitochondrial genes and multiple structural subunits encoded by nuclear genes. The mitochondrially-encoded subunits function in electron transfer, and the nuclear-encoded subunits may function in the regulation and assembly of the complex. This nuclear gene encodes heme A:farnesyltransferase, which is not a structural subunit but required for the expression of functional COX and functions in the maturation of the heme A prosthetic group of COX. This protein is predicted to contain 7-9 transmembrane domains localized in the mitochondrial inner membrane. A gene mutation, which results in the substitution of a lysine for an asparagine (N204K), is identified to be responsible for cytochrome c oxidase deficiency. In addition, this gene is disrupted in patients with CMT1A (Charcot-Marie-Tooth type 1A) duplication and with HNPP (hereditary neuropathy with liability to pressure palsies) deletion.

UOM: 1 * 400 µl

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Artikel-Nr: (PHR2349-300MG)

Lieferant: Merck

Hersteller Artikel Nummer : PHR2349-300MG

Beschreibung: ASPARAGINE ANHYDROUS 1 * 300 mg

UOM: 1 * 300 mg

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Artikel-Nr: (PHR2350-300MG)

Lieferant: Merck

Hersteller Artikel Nummer : PHR2350-300MG

Beschreibung: ASPARAGINE MONOHYDRATE 1 * 300 mg

UOM: 1 * 300 mg

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Artikel-Nr: (APOSOR1012759-500G)

Lieferant: Apollo Scientific

Hersteller Artikel Nummer : OR1012759-500G

Beschreibung: D-Asparagine 500g pack 1 * 500 g

UOM: 1 * 500 g

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Artikel-Nr: (APOSOR1012759-2.5)

Lieferant: Apollo Scientific

Hersteller Artikel Nummer : OR1012759-2.5

Beschreibung: D-Asparagine 2.5kg pack 1 * 2,5 kg

UOM: 1 * 2,5 kg

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