C20orf7 antibody (AA 196-345)

Catalog No. ABIN6144470

Product Details anti-C20orf7 Antibody

Target: C20orf7 (Chromosome 20 Open Reading Frame 7 (C20orf7))

Binding Specificity: AA 196-345

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This C20orf7 antibody is un-conjugated

Application: Western Blotting (WB), Immunohistochemistry (IHC)

Sequence: ELRCSLQLAE TEREGGFSPH ISPFTAVNDL GHLLGRAGFN TLTVDTDEIQ VNYPGMFELM EDLQGMGESN CAWNRKALLH RDTMLAAAAV YREMYRNEDG SVPATYQIYY MIGWKYHESQ ARPAERGSAT VSFGELGKIN NLMPPGKKSQ

Cross-Reactivity: Human, Mouse, Rat

Characteristics: Polyclonal Antibodies

Immunogen: Recombinant fusion protein containing a sequence corresponding to amino acids 196-345 of human NDUFAF5 (NP_077025.2).

Isotype: IgG

Application Details

Application Notes: WB,1:500 - 1:2000,IHC,1:50 - 1:200

Comment:

HIGH QUALITY

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 C20orf7

Target: C20orf7 (Chromosome 20 Open Reading Frame 7 (C20orf7))

Alternative Name: NDUFAF5 (C20orf7 Products)

Synonyms: C20orf7 antibody, bA526K24.2 antibody, dJ842G6.1 antibody, 2310003L22Rik antibody, zgc:162919 antibody, RGD1309829 antibody, NADH:ubiquinone oxidoreductase complex assembly factor 5 antibody, NADH dehydrogenase (ubiquinone) complex I, assembly factor 5 antibody, NDUFAF5 antibody, ndufaf5 antibody, Ndufaf5 antibody

Background: The NADH-ubiquinone oxidoreductase complex (complex I) of the mitochondrial respiratory chain catalyzes the transfer of electrons from NADH to ubiquinone, and consists of at least 43 subunits. The complex is located in the inner mitochondrial membrane. This gene encodes a mitochondrial protein that is associated with the matrix face of the mitochondrial inner membrane and is required for complex I assembly. A mutation in this gene results in mitochondrial complex I deficiency. Multiple transcript variants encoding different isoforms have been found for this gene.,NDUFAF5,C20orf7,bA526K24.2,dJ842G6.1,Epigenetics & Nuclear Signaling,NDUFAF5

Molecular Weight: 36 kDa/38 kDa

Gene ID: 79133

UniProt: Q5TEU4