NDUFB3 antibody (AA 1-98)

Catalog No. ABIN7268810

Product Details anti-NDUFB3 Antibody

Target: NDUFB3 (NADH Dehydrogenase (Ubiquinone) 1 beta Subcomplex, 3, 12kDa (NDUFB3))

Binding Specificity: AA 1-98

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This NDUFB3 antibody is un-conjugated

Application: Western Blotting (WB), Immunofluorescence (IF)

Purpose: NDUFB3 Rabbit pAb

Sequence: MAHEHGHEHG HHKMELPDYR QWKIEGTPLE TIQKKLAAKG LRDPWGRNEA WRYMGGFAKS VSFSDVFFKG FKWGFAAFVV AVGAEYYLES LNKDKKHH

Cross-Reactivity: Human, Mouse

Characteristics: Polyclonal Antibodies

Purification: Affinity purification

Immunogen: Recombinant fusion protein containing a sequence corresponding to amino acids 1-98 of human NDUFB3 (NP_002482.1).

Isotype: IgG

Application Details

Application Notes: WB,1:500 - 1:2000,IF,1:50 - 1:100

Restrictions: For Research Use only

Handling

Format: Liquid

Buffer: PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

Preservative: Sodium azide

Precaution of Use: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: -20 °C

Storage Comment: Store at -20°C. Avoid freeze / thaw cycles.

Target Details for NDUFB3

Target: NDUFB3 (NADH Dehydrogenase (Ubiquinone) 1 beta Subcomplex, 3, 12kDa (NDUFB3))

Alternative Name: NDUFB3 (NDUFB3 Products)

Synonyms: NDUFB3 antibody, 2700033I16Rik antibody, AI415450 antibody, B12 antibody, CI-B12 antibody, NADH:ubiquinone oxidoreductase subunit B3 antibody, NADH:ubiquinone oxidoreductase subunit B3 S homeolog antibody, NADH dehydrogenase (ubiquinone) 1 beta subcomplex, 3, 12kDa antibody, NADH dehydrogenase (ubiquinone) 1 beta subcomplex 3 antibody, Ndufb3 antibody, NDUFB3 antibody, ndufb3.S antibody, ndufb3 antibody

Background: This gene encodes an accessory subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (Complex I) which is the first enzyme in the electron transport chain of mitochondria. This protein localizes to the inner membrane of the mitochondrion as a single-pass membrane protein. Mutations in this gene contribute to mitochondrial complex 1 deficiency. Alternative splicing results in multiple transcript variants encoding the same protein. Humans have multiple pseudogenes of this gene.,NDUFB3,B12,CI-B12,Cancer,Signal Transduction,Endocrine & Metabolism,Mitochondrial metabolism,Mitochondrial markers,Oxidative phosphorylation,Neuroscience,Neurodegenerative Diseases,NDUFB3

Molecular Weight: 11kDa

Gene ID: 4709

UniProt: O43676