SCCPDH antibody

Catalog No. ABIN7260229

Product Details anti-SCCPDH Antibody

Target: SCCPDH (Saccharopine Dehydrogenase (SCCPDH))

Reactivity: Human, Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This SCCPDH antibody is un-conjugated

Application: Western Blotting (WB)

Characteristics: Polyclonal Antibody

Purification: Affinity purification

Immunogen: Recombinant fusion protein of human SCCPDH (NP_057086.2).

Isotype: IgG

Application Details

Application Notes: WB 1:500-1:2000

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 mg/mL

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 SCCPDH

Target: SCCPDH (Saccharopine Dehydrogenase (SCCPDH))

Alternative Name: SCCPDH (SCCPDH Products)

Synonyms: NET11 antibody, RP11-439E19.2 antibody, AW214504 antibody, C330023F11Rik antibody, RGD1311440 antibody, fb63c02 antibody, zgc:92525 antibody, wu:fb63c02 antibody, MGC82870 antibody, DKFZp469I2131 antibody, cb4 antibody, sb:cb4 antibody, zgc:101527 antibody, saccharopine dehydrogenase (putative) antibody, saccharopine dehydrogenase a antibody, saccharopine dehydrogenase (putative) S homeolog antibody, saccharopine dehydrogenase b antibody, SCCPDH antibody, Sccpdh antibody, sccpdha antibody, sccpdh.S antibody, sccpdh antibody, sccpdhb antibody

Background: SCCPDH (Probable saccharopine dehydrogenase) is a 429 amino acid protein that belongs to the saccharopine dehydrogenase family. The SCCPDH gene is conserved in chimpanzee, dog, cow, mouse, rat, chicken, fruit fly, mosquito and C.elegans, and maps to human chromosome 1q44. Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8 % of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma.

Molecular Weight:

Observed_MW: 45 kDa

Calculated_MW: 47 kDa

Gene ID: 51097

UniProt: Q8NBX0

Pathways: SARS-CoV-2 Protein Interactome