SAYSD1 antibody (AA 130-180)

Catalog No. ABIN1385609

Product Details anti-SAYSD1 Antibody

Target: SAYSD1 (SAYSVFN Motif Domain Containing 1 (SAYSD1))

Binding Specificity: AA 130-180

Reactivity: Human, Rat, Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This SAYSD1 antibody is un-conjugated

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

Cross-Reactivity: Human, Mouse, Rat

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C6orf64

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 SAYSD1

Target: SAYSD1 (SAYSVFN Motif Domain Containing 1 (SAYSD1))

Alternative Name: C6orf64 (SAYSD1 Products)

Synonyms: C6orf64 antibody, SAYSD1 antibody, C23H6orf64 antibody, 1810063B07Rik antibody, 4930488P03Rik antibody, SAYSVFN motif domain containing 1 antibody, SAYSD1 antibody, Saysd1 antibody

Background:

Synonyms: Chromosome 6 open reading frame 64, DKFZp434H012, FLJ11101, Hypothetical protein LOC55776, Uncharacterized protein C6orf64, SMDC1_HUMAN, SAYSD1, SAYSvFN domain-containing protein 1

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. The C6orf64 gene product has been provisionally designated C6orf64 pending further characterization.

Gene ID: 55776

UniProt: Q9NPB0