ZUFSP antibody

Catalog No. ABIN7249124

Product Details anti-ZUFSP Antibody

Target: ZUFSP (Zinc Finger with UFM1-Specific Peptidase Domain (ZUFSP))

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This ZUFSP antibody is un-conjugated

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

Characteristics: Polyclonal Antibody

Purification: Antigen affinity purification

Immunogen: Fusion protein of human ZUFSP

Isotype: IgG

Application Details

Application Notes: WB 1:500-1:2000, IHC 1:25-1:100, ELISA 1:5000-1:10000

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 0.7 mg/mL

Buffer: PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4

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 ZUFSP

Target: ZUFSP (Zinc Finger with UFM1-Specific Peptidase Domain (ZUFSP))

Alternative Name: ZUFSP (ZUFSP Products)

Synonyms: ZUFSP antibody, MGC83919 antibody, im:7145879 antibody, zgc:158611 antibody, C6orf113 antibody, dJ412I7.3 antibody, C9H6orf113 antibody, 2700019D07Rik antibody, RGD1307672 antibody, zinc finger with UFM1 specific peptidase domain antibody, zinc finger with UFM1-specific peptidase domain S homeolog antibody, zinc finger with UFM1-specific peptidase domain antibody, ZUFSP antibody, zufsp.S antibody, zufsp antibody, Zufsp antibody

Background: Making up nearly 6 % of the human genome, chromosome 6 contains around 1,200 genes within 170 million base pairs of sequence. Deletion of a portion of the q arm of chromosome 6 is associated with early onset intestinal cancer suggesting the presence of a cancer susceptibility locus. Porphyria cutanea tarda is associated with chromosome 6 through the HFE gene which, when mutated, predisposes an individual to developing this porphyria. Notably, the PARK2 gene, which is associated with Parkinson's disease, and the genes encoding the major histocompatiblity complex proteins, which are key molecular components of the immune system and determine predisposition to rheumatic diseases, are also located on chromosome 6. Stickler syndrome, 21-hydroxylase deficiency and maple syrup urine disease are also associated with genes on chromosome 6. A bipolar disorder susceptibility locus has been identified on the q arm of chromosome 6.

Molecular Weight:

Observed_MW: Refer to figures

Calculated_MW: 66 kDa

UniProt: Q96AP4