NDUFB11 antibody (AA 1-163)

Catalog No. ABIN7268809

Product Details anti-NDUFB11 Antibody

Target: NDUFB11 (NADH Dehydrogenase (Ubiquinone) 1 beta Subcomplex, 11, 17.3kDa (NDUFB11))

Binding Specificity: AA 1-163

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This NDUFB11 antibody is un-conjugated

Application: Western Blotting (WB)

Purpose: NDUFB11 Rabbit pAb

Sequence: MAAGLFGLSA RRLLAAAATR GLPAARVRWE SSFSRTVVAP SAVAGKRPPE PTTPWQEDPE PEDENLYEKN PDSHGYDKDP VLDVWNMRLV FFFGVSIILV LGSTFVAYLP DYRCTGCPRA WDGMKEWSRR EAERLVKYRE ANGLPIMESN CFDPSKIQLP EDE

Cross-Reactivity: Human, Mouse, Rat

Characteristics: Polyclonal Antibodies

Purification: Affinity purification

Immunogen: Recombinant fusion protein containing a sequence corresponding to amino acids 1-163 of human NDUFB11 (NP_061929.2).

Isotype: IgG

Application Details

Application Notes: WB,1:500 - 1:2000

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 NDUFB11

Target: NDUFB11 (NADH Dehydrogenase (Ubiquinone) 1 beta Subcomplex, 11, 17.3kDa (NDUFB11))

Alternative Name: NDUFB11 (NDUFB11 Products)

Synonyms: CI-ESSS antibody, ESSS antibody, NP17.3 antibody, Np15 antibody, P17.3 antibody, D5Bwg0566e antibody, D5Bwg0577e antibody, NP15.6 antibody, RGD1563698 antibody, NADH:ubiquinone oxidoreductase subunit B11 antibody, NADH dehydrogenase (ubiquinone) 1 beta subcomplex, 11 antibody, NDUFB11 antibody, Ndufb11 antibody

Background: The protein encoded by this gene is a subunit of the multisubunit NADH:ubiquinone oxidoreductase (complex I). Mammalian complex I is located at the mitochondrial inner membrane. This protein has NADH dehydrogenase activity and oxidoreductase activity. It transfers electrons from NADH to ubiquinone. Mutations in the human gene are associated with linear skin defects with multiple congenital anomalies 3 and mitochondrial complex I deficiency.,NDUFB11,CI-ESSS,ESSS,NP17.3,Np15,P17.3,Neuroscience,Neurodegenerative Diseases,NDUFB11

Molecular Weight: 17kDa/18kDa

Gene ID: 54539

UniProt: Q9NX14