RBMX2 antibody (AA 21-100) (Biotin)

Catalog No. ABIN1701455

The Rabbit Polyclonal anti-RBMX2 antibody has been validated for ELISA, IHC (p) and IHC (fro). It is suitable to detect RBMX2 in samples from Human.

Quick Overview for RBMX2 antibody (AA 21-100) (Biotin) (ABIN1701455)

Target: RBMX2 (RNA Binding Motif Protein, X-Linked 2 (RBMX2))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This RBMX2 antibody is conjugated to Biotin

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

Product Details anti-RBMX2 Antibody (Biotin)

Binding Specificity: AA 21-100

Predicted Reactivity: Human,Mouse,Rat,Cow,Sheep,Pig,Horse,Chicken,Rabbit

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human RBMX2

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 RBMX2

Target: RBMX2 (RNA Binding Motif Protein, X-Linked 2 (RBMX2))

Alternative Name: RBMX2

Background:

Synonyms: RNA-binding mot protein, X-linked 2, CGI-79, CGI 79, Rbmx2, RBMX2_HUMAN, RNA binding mot protein X linked 2, RNA-binding mot protein, X-linked 2.

Background: RBMX2 is a 322 amino acid member of the IST3 family that contains one RRM (RNA recognition motif) domain. The RBMX2 gene is intronless, conserved in chimpanzee, dog, cow, mouse, rat, zebrafish, fruit fly, mosquito, C.elegans, S.pombe, S.cerevisiae, K.lactis, E.gossypii, M.grisea, N.crassa, A.thaliana, rice and P.falciparum, and maps to human chromosome Xq25. The X and Y chromosomes are the human sex chromosomes. Chromosome X consists of about 153 million base pairs and nearly 1,000 genes. The combination of an X and Y chromosome lead to normal male development while two copies of X lead to normal female development. More than one copy of the X chromosome with a Y chromosome causes Klinefelter's syndrome. A single copy of X alone leads to Turner's syndrome. More than 2 copies of the X chromosome, in the absence of a Y chromosome, is known as Triple X syndrome. Color blindness, hemophilia, and Duchenne muscular dystrophy are well known X chromosome-linked conditions that affect males more frequently as males carry a single X chromosome.