SLAIN1 antibody (AA 1-100) (Biotin)

Catalog No. ABIN1700397

This anti-SLAIN1 antibody is a Rabbit Polyclonal antibody detecting SLAIN1 in ELISA, IHC (p) and IHC (fro). Suitable for Human.

Quick Overview for SLAIN1 antibody (AA 1-100) (Biotin) (ABIN1700397)

Target: SLAIN1 (SLAIN Motif Family, Member 1 (SLAIN1))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This SLAIN1 antibody is conjugated to Biotin

Application: ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))

Product Details anti-SLAIN1 Antibody (Biotin)

Binding Specificity: AA 1-100

Predicted Reactivity: Human,Mouse,Rat,Dog,Chicken,Rabbit

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human SLAIN1/C13orf32

Isotype: IgG

Application Details

Application Notes: IHC-P 1:200-400
IHC-F 1:100-500

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % 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: -20 °C

Storage Comment: Store at -20°C for 12 months.

Expiry Date: 12 months

Target Details for SLAIN1

Target: SLAIN1 (SLAIN Motif Family, Member 1 (SLAIN1))

Alternative Name: SLAIN1

Background:

Synonyms: C13orf32, chromosome 13 open reading frame 32, FLJ30046, MGC131899, SLAI1_HUMAN, SLAIN mot family member 1, SLAIN mot family, member 1, SLAIN mot-containing protein 1, Slain1.

Background: SLAIN1 is a 561 amino acid member of the SLAIN motif-containing family and is expressed in embryonic stem cells, as well as in lung, brain and testis, where it exists as two alternatively spliced isoforms. The gene encoding SLAIN1 maps to human chromosome 13, which houses over 400 genes, such as BRCA2 and RB1, and comprises nearly 4 % of the human genome. As with most chromosomes, polysomy of part or all of chromosome 13 is deleterious to development and decreases the odds of survival. Trisomy 13, also known as Patau syndrome, is deadly and the few who survive past one year suffer from permanent neurologic defects, difficulty eating and vulnerability to serious respiratory infections.