NDUFV2 Monoclonal antibody

NDUFV2 Monoclonal Antibody for IHC, WB, ELISA

Host / Isotype

Mouse / IgG1

Reactivity

Human, Mouse, Rat, Rabbit, Pig, Chicken

Applications

WB, IHC, ELISA

Conjugate

Unconjugated

CloneNo.

3B4A5

Cat no : 68150-1-Ig

Synonyms

NDUFV2



Tested Applications

Positive WB detected inJurkat cells, chicken heart tissue, HeLa cells, pig brain tissue, rabbit brain tissue, rat brain tissue, mouse brain tissue
Positive IHC detected inmouse heart 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 : 1:5000-1:50000
Immunohistochemistry (IHC)IHC : 1:500-1:2000
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.

Product Information

68150-1-Ig targets NDUFV2 in WB, IHC, ELISA applications and shows reactivity with Human, Mouse, Rat, Rabbit, Pig, Chicken samples.

Tested Reactivity Human, Mouse, Rat, Rabbit, Pig, Chicken
Host / Isotype Mouse / IgG1
Class Monoclonal
Type Antibody
Immunogen NDUFV2 fusion protein Ag7760
Full Name NADH dehydrogenase (ubiquinone) flavoprotein 2, 24kDa
Calculated Molecular Weight 27 kDa
Observed Molecular Weight24-27 kDa
GenBank Accession NumberBC001632
Gene Symbol NDUFV2
Gene ID (NCBI) 4729
Conjugate Unconjugated
Form Liquid
Purification MethodProtein G 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.

Background Information

The NDUFV2 gene encodes the 24-kD subunit of the mitochondrial NADH: ubiquinone oxidoreductase (complex I of the respiratory chain). The protein belongs to the complex I 24 kDa subunit family. It is the core subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (Complex I) that is believed to belong to the minimal assembly required for catalysis. NDUFV2 constitutes one genetic risk factor for PD, and the mutation may well be a cause of complex I deficiency in this disease(PMID:9570948).

Protocols

Product Specific Protocols
WB protocol for NDUFV2 antibody 68150-1-IgDownload protocol
IHC protocol for NDUFV2 antibody 68150-1-IgDownload protocol
Standard Protocols
Click here to view our Standard Protocols