USMG5 Polyclonal antibody

USMG5 Polyclonal Antibody for WB, IHC, ELISA

Host / Isotype

Rabbit / IgG

Reactivity

human, mouse, rat

Applications

WB, IF, IHC, ELISA

Conjugate

Unconjugated

Cat no : 17716-1-AP

Synonyms

HCV F transactivated protein 2, HCVFTP2, USMG5



Tested Applications

Positive WB detected inmouse brain tissue, human liver tissue, human brain tissue, rat brain tissue
Positive IHC detected inmouse brain tissue, human placenta tissue
Note: suggested antigen retrieval with TE buffer pH 9.0; (*) Alternatively, antigen retrieval may be performed with citrate buffer pH 6.0

Recommended dilution

ApplicationDilution
Western Blot (WB)WB : 1:500-1:1000
Immunohistochemistry (IHC)IHC : 1:50-1:500
Sample-dependent, check data in validation data gallery

Product Information

17716-1-AP targets USMG5 in WB, IF, IHC, ELISA applications and shows reactivity with human, mouse, rat samples.

Tested Reactivity human, mouse, rat
Cited Reactivity mouse
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen USMG5 fusion protein Ag12086 相同性解析による交差性が予測される生物種
Full Name up-regulated during skeletal muscle growth 5 homolog (mouse)
Calculated molecular weight 58 aa, 7 kDa
Observed molecular weight 6 kDa
GenBank accession numberBC072683
Gene symbol USMG5
Gene ID (NCBI) 84833
RRIDAB_2214288
Conjugate Unconjugated
Form Liquid
Purification Method Antigen 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.

Protocols

Product Specific Protocols
WB protocol for USMG5 antibody 17716-1-APDownload protocol
IHC protocol for USMG5 antibody 17716-1-APDownload protocol
Standard Protocols
Click here to view our Standard Protocols

Publications

SpeciesApplicationTitle
mouseWB

J Clin Invest

Deficiency in Kelch protein Klhl31 causes congenital myopathy in mice.

Authors - James B Papizan
mouseIF

Sci Rep

miR-379 links glucocorticoid treatment with mitochondrial response in Duchenne muscular dystrophy.

Authors - M Sanson