MSANTD1 antibody (AA 50-100)

Catalog No. ABIN1385556

This anti-MSANTD1 antibody is a Rabbit Polyclonal antibody detecting MSANTD1 in WB, IF (p) and IHC (p). Suitable for Human, Mouse and Rat.

Quick Overview for MSANTD1 antibody (AA 50-100) (ABIN1385556)

Target: MSANTD1 (Myb/SANT-Like DNA-Binding Domain Containing 1 (MSANTD1))

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This MSANTD1 antibody is un-conjugated

Application: Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Product Details anti-MSANTD1 Antibody

Binding Specificity: AA 50-100

Cross-Reactivity: Human, Mouse, Rat

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C4orf44

Isotype: IgG

Application Details

Application Notes: WB 1:300-5000
IHC-P 1:200-400
IF(IHC-P) 1:50-200

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 μg/μL

Buffer: 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.

Preservative: ProClin

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

Storage: 4 °C,-20 °C

Storage Comment: Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.

Expiry Date: 12 months

Target Details for MSANTD1

Target: MSANTD1 (Myb/SANT-Like DNA-Binding Domain Containing 1 (MSANTD1))

Alternative Name: C4orf44

Background:

Synonyms: C4orf44, Myb/SANT-like DNA-binding domain-containing protein 1, MSANTD1

Background: Representing approximately 6 % of the human genome, chromosome 4 contains nearly 900 genes. Notably, the Huntingtin gene, which is found to encode an expanded glutamine tract in cases of Huntington's disease, is on chromosome 4. FGFR-3 is also encoded on chromosome 4 and has been associated with thanatophoric dwarfism, achondroplasia, Muenke syndrome and bladder cancer. Chromosome 4 is also tied to Ellis-van Creveld syndrome, methylmalonic acidemia and polycystic kidney disease. Chromosome 4 reportedly contains the largest gene deserts (regions of the genome with no protein encoding genes) and has one of the two lowest recombination frequencies of the human chromosomes. The C4orf44 gene product has been provisionally designated C4orf44 pending further characterization.

Gene ID: 345222

UniProt: Q6ZTZ1