Recombinant Human DHRS9 293 Cell Lysate

• Cat.No.: DHRS9-6934HCL

Specification

• Description: Antigen standard for dehydrogenase/reductase (SDR family) member 9 (DHRS9), transcript variant 2 is a lysate prepared from HEK293T cells transiently transfected with a TrueORF gene-carrying pCMV plasmid and then lysed in RIPA Buffer. Protein concentration was determined using a colorimetric assay. The antigen control carries a C-terminal Myc/DDK tag for detection.
• Source: HEK 293 cells
• Species: Human
• Components: This product includes 3 vials: 1 vial of gene-specific cell lysate, 1 vial of control vector cell lysate, and 1 vial of loading buffer. Each lysate vial contains 0.1 mg lysate in 0.1 ml (1 mg/ml) of RIPA Buffer (50 mM Tris-HCl pH7.5, 250 mM NaCl, 5 mM EDTA, 50 mM NaF, 1% NP40). The loading buffer vial contains 0.5 ml 2X SDS Loading Buffer (125 mM Tris-Cl, pH6.8, 10% glycerol, 4% SDS, 0.002% Bromophenol blue, 5% beta-mercaptoethanol).
• Size: 0.1 mg
• Storage Instruction: Store at -80°C. Minimize freeze-thaw cycles. After addition of 2X SDS Loading Buffer, the lysates can be stored at -20°C. Product is guaranteed 6 months from the date of shipment.
• Applications: ELISA, WB, IP. WB: Mix equal volume of lysates with 2X SDS Loading Buffer. Boil the mixture for 10 min before loading (for membrane protein lysates, incubate the mixture at room temperature for 30 min). Load 5 ug lysate per lane.

Gene Information

• Gene Name: DHRS9 dehydrogenase/reductase (SDR family) member 9 [ Homo sapiens ]
• Official Symbol: DHRS9
• Synonyms: DHRS9; dehydrogenase/reductase (SDR family) member 9; dehydrogenase/reductase SDR family member 9; 3 alpha hydroxysteroid dehydrogenase; 3alpha HSD; NADP dependent retinol dehydrogenase/reductase; RDH15; RDHL; retinol dehydrogenase homolog; RETSDR8; SDR9C4; short chain dehydrogenase/reductase family 9C; member 4; RDH-E2; 3-alpha-HSD; 3-alpha hydroxysteroid dehydrogenase; short-chain dehydrogenase/reductase retSDR8; NADP-dependent retinol dehydrogenase/reductase; short chain dehydrogenase/reductase family 9C, member 4; RDHTBE; 3ALPHA-HSD
• Gene ID: 10170
• mRNA Refseq: NM_001142270
• Protein Refseq: NP_001135742
• MIM: 612131
• UniProt ID: Q9BPW9
• Chromosome Location: 2q31.1
• Pathway: Metabolic pathways, organism-specific biosystem; Retinol metabolism, organism-specific biosystem; Retinol metabolism, conserved biosystem; retinol biosynthesis, conserved biosystem; retinol biosynthesis, organism-specific biosystem; the visual cycle, conserved biosystem; the visual cycle, organism-specific biosystem
• Function: alcohol dehydrogenase (NAD) activity; nucleotide binding; oxidoreductase activity; racemase and epimerase activity; retinol dehydrogenase activity; testosterone dehydrogenase (NAD+) activity

Reviews

10/24/2022

DHRS9 is highly specific and active, and does not cause abnormal immune responses.

04/22/2022

The product is very mature and can be used for scientific research.

10/19/2020

The solubility is very good and can be easily dissolved in a variety of buffers.

Q&As

Can lifestyle changes reduce the risk for DHRS9 mutations?

There is currently no definitive way to alter the variation of the DHRS9 gene. However, healthy lifestyles, such as a balanced diet, moderate exercise, and good social interactions, may help reduce the risk of neurological disorders, although they may not directly improve the effects of the DHRS9 gene variant.

What is the effect of mutations in the DHRS9 gene?

Mutations in the DHRS9 gene may cause abnormal function of retinoic acid-binding protein 1, which in turn affects retinoic acid metabolism and may increase the risk of neurological diseases.

Are DHRS9 gene variants associated with cognitive function

Studies have shown that mutations in the DHRS9 gene may affect cognitive function, but the specific mechanism still needs further research.

What might be involved in future studies of the DHRS9 gene?

Future research on the DHRS9 gene may involve more in-depth studies of molecular mechanisms, disease associations, and the development of therapeutics for this gene variant.

Are variants in the DHRS9 gene associated with behavioral traits?

Studies have shown that mutations in the DHRS9 gene may be associated with certain behavioral traits, such as social skills, attention, and impulse control.

How to detect variants in the DHRS9 gene?

Variants in the DHRS9 gene, including single nucleotide polymorphisms (SNPs), insertions/deletions, etc., can be detected by gene sequencing technology.