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MRPS7 Polyclonal antibody

MRPS7 Polyclonal Antibody for WB, ELISA

Host / Isotype

Rabbit / IgG

Reactivity

human

Applications

WB, ELISA

Conjugate

Unconjugated

Cat no : 26828-1-AP

Synonyms

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

Validation Data Gallery

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  • Western Blot (WB) analysis of various lysates using MRPS7 Polyclonal antibody (26828-1-AP)

    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.

Tested Applications

Positive WB detected inHepG2 cells, PC-3 cells

Recommended dilution

ApplicationDilution
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

WBSee 3 publications below

Product Information

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

Tested Reactivity human
Cited Reactivityhuman
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 NumberBC000241
Gene Symbol MRPS7
Gene ID (NCBI) 51081
RRIDAB_2880650
Conjugate Unconjugated
Form Liquid
Purification MethodAntigen affinity purification
Storage Buffer PBS with 0.02% sodium azide and 50% glycerol pH 7.3.
Storage ConditionsStore at -20°C. Stable for one year after shipment. Aliquoting is unnecessary for -20oC storage. 20ul sizes contain 0.1% BSA.

Protocols

Product Specific Protocols
WB protocol for MRPS7 antibody 26828-1-APDownload protocol
Standard Protocols
Click here to view our Standard Protocols

Publications

SpeciesApplicationTitle
humanWB

Nature

SLC25A39 is necessary for mitochondrial glutathione import in mammalian cells.

Authors - Ying Wang
View Article
humanWB

Hum Genet

Deficiency of the mitochondrial ribosomal subunit, MRPL50, causes autosomal recessive syndromic premature ovarian insufficiency

Authors - Shabnam Bakhshalizadeh
View Article
humanWB

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
View Article