MRPS7 Polyclonal antibody

MRPS7 Polyclonal Antibody for WB, ELISA

Host / Isotype

Rabbit / IgG

Reactivity

human

Applications

WB, ELISA

Conjugate

Unconjugated

Publications

3

Cat no : 26828-1-AP

Synonyms

bMRP 27a, bMRP27a, MRP S, MRP S7, MRPS7, RP S7, RPMS7, S7mt

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Validation Data Gallery

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  WB analysis using 26828-1-AP

  Various lysates were subjected to SDS PAGE followed by western blot with 26828-1-AP (MRPS7 antibody) at dilution of 1:20000 incubated at room temperature for 1.5 hours.

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Tested Applications

• Positive WB detected in: HepG2 cells, PC-3 cells

Recommended dilution

• Western Blot (WB): WB : 1:5000-1:50000

It is recommended that this reagent should be titrated in each testing system to obtain optimal results.

Sample-dependent, Check data in validation data gallery.

Published Applications

• WB: See 3 publications below

Product Information

26828-1-AP targets MRPS7 in WB, ELISA applications and shows reactivity with human samples.

• Tested Reactivity: human
• Cited Reactivity: human
• Host / Isotype: Rabbit / IgG
• Class: Polyclonal
• Type: Antibody
• Immunogen: MRPS7 fusion protein Ag25325
• Full Name: mitochondrial ribosomal protein S7
• Calculated Molecular Weight: 28 kDa
• Observed Molecular Weight: 27 kDa
• GenBank Accession Number: BC000241
• Gene Symbol: MRPS7
• Gene ID (NCBI): 51081
• RRID: AB_2880650
• Conjugate: Unconjugated
• Form: Liquid
• Purification Method: Antigen affinity purification
• Storage Buffer: PBS with 0.02% sodium azide and 50% glycerol pH 7.3.
• Storage Conditions: Store at -20°C. Stable for one year after shipment. Aliquoting is unnecessary for -20^oC storage. 20ul sizes contain 0.1% BSA.

Publications

Species	Application	Title
human	WB	Nature; SLC25A39 is necessary for mitochondrial glutathione import in mammalian cells.; Authors - Ying Wang
human	WB	Hum Genet; Deficiency of the mitochondrial ribosomal subunit, MRPL50, causes autosomal recessive syndromic premature ovarian insufficiency; Authors - Shabnam Bakhshalizadeh
human	WB	Hum Mol Genet; Multi-omics identifies large mitoribosomal subunit instability caused by pathogenic MRPL39 variants as a cause of pediatric onset mitochondrial disease; Authors - Sumudu S C Amarasekera