ZC3H11A antibody (Zinc Finger CCCH-Type Containing 11A) (AA 339-384)

Catalog No. ABIN6713899

Product Details anti-ZC3H11A Antibody

Target:

ZC3H11A

Binding Specificity: AA 339-384

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Application: Western Blotting (WB)

Specificity: ZC3H11A polyclonal antibody detects endogenous levels of ZC3H11A protein.

Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Purity: > 95% (by SDS-PAGE)

Immunogen: Synthetic peptide, corresponding to amino acids 339-384 of Human ZC3H11A.

Application Details

Application Notes: WB: 1:500~1:1000

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 mg/mL

Buffer: 1 mg/mL in Phosphate buffered saline (PBS) with 0.05 % sodium azide, approx. pH 7.2.

Preservative: Sodium azide

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

Handling Advice: Avoid freeze-thaw cycles.

Storage: 4 °C,-20 °C

Storage Comment: Store at 4°C short term. Aliquot and store at -20°C long term.

Target Details for ZC3H11A

Target:

ZC3H11A

Alternative Name: ZC3H11A

Synonyms: ZC3HDC11A, 1110003F06Rik, 5730454B08Rik, G630041M05Rik, Zc3hdc11a, Zc3hh11a, mKIAA0663, RGD1308290, ZC3H11B, MGC142959, fc32e10, wu:fc32e10, zgc:73328, zinc finger CCCH-type containing 11A, zinc finger CCCH type containing 11A, zinc finger CCCH-type containing 11A S homeolog, ZC3H11A, Zc3h11a, zc3h11a, zc3h11a.S

Background: ZC3H11A (zinc finger CCCH domain-containing protein 11A), also known as KIAA0663 or ZC3HDC11A, is an 810 amino acid protein that contains 3 C3 H1-type zinc fingers. ZC3H11A is expressed in heart, brain, liver, skeletal muscle, kidney, pancreas, spleen, testis, ovary, fetal brain and fetal liver. The gene encoding ZC3H11A maps to human chromosome 1q32.1 and mouse chromosome 1 E4. Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8 % of the human genome. The rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene on chromosome 1 which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1.

Molecular Weight: ~ 89 kDa

UniProt: O75152