Delta-1-Pyrroline-5-Carboxylate Synthase (ALDH18A1) Peptide

Este producto es parte de ALDH - Aldehyde dehydrogenase family member
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195€ (100 µg)

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935106861
info@markelab.com
name
Delta-1-Pyrroline-5-Carboxylate Synthase (ALDH18A1) Peptide
category
Proteins and Peptides
provider
Abbexa
reference
abx616402
tested applications
P-ELISA

Description

Delta-1-Pyrroline-5-Carboxylate Synthase (ALDH18A1) Peptide is a synthetic peptide. This peptide is used in the production of

Documents del producto

Instrucciones
Data sheet
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Product specifications

Category
Proteins and Peptides
Immunogen Target
Delta-1-Pyrroline-5-Carboxylate Synthase (ALDH18A1)
Host
Synthetic
Assay Type
Activity: Not tested.
Sequence Fragment: C-Terminus: C-SEHGSLKYLH
Recommended Dilution
BL (predicted): 0.5 mg/ml. Optimal dilutions/concentrations should be determined by the end user.
Conjugation
Unconjugated
Size 1
100 µg
Form
Lyophilized
Tested Applications
P-ELISA
Buffer
Prior to lyophilization: Deionized water.
Availability
Shipped within 5-10 working days.
Storage
Aliquot and store at -20 °C. Avoid repeated freeze/thaw cycles.
Dry Ice
No
Gene ID
5832, 56454, 361755
NCBI Accession
NP_002851.2, NP_001017423.1
Alias
P5CS,Aldehyde dehydrogenase family 18 member A1
Background
Protein ALDH18A1
Status
RUO
Note
THIS PRODUCT IS FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC, THERAPEUTIC OR COSMETIC PROCEDURES. NOT FOR HUMAN OR ANIMAL CONSUMPTION.
Reconstitute in deionized water.

Descripción

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Delta-1-Pyrroline-5-Carboxylate Synthase (ALDH18A1) Antibody

ALDH18A1 Antibody is a Rabbit Polyclonal antibody against ALDH18A1. This gene is a member of the aldehyde dehydrogenase family and encodes a bifunctional ATP- and NADPH-dependent mitochondrial enzyme with both gamma-glutamyl kinase and gamma-glutamyl phosphate reductase activities. The encoded protein catalyzes the reduction of glutamate to delta1-pyrroline-5-carboxylate, a critical step in the de novo biosynthesis of proline, ornithine and arginine. Mutations in this gene lead to hyperammonemia, hypoornithinemia, hypocitrullinemia, hypoargininemia and hypoprolinemia and may be associated with neurodegeneration, cataracts and connective tissue diseases. Alternatively spliced transcript variants, encoding different isoforms, have been described for this gene.

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