CXorf21 antibody (AA 165-215) (Cy7)

Catalog No. ABIN1421252

The Rabbit Polyclonal anti-CXorf21 antibody is suitable to detect CXorf21 in samples from Human. It has been validated for FACS and IF (p).

Quick Overview for CXorf21 antibody (AA 165-215) (Cy7) (ABIN1421252)

Target: CXorf21 (TASL) (TLR Adaptor Interacting With Endolysosomal SLC15A4 (TASL))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This CXorf21 antibody is conjugated to Cy7

Application: Flow Cytometry (FACS), Immunofluorescence (Paraffin-embedded Sections) (IF (p))

Product Details anti-CXorf21 Antibody (Cy7)

Binding Specificity: AA 165-215

Purpose: CXorf21 Polyclonal Antibody, Cy7 Conjugated

Cross-Reactivity: Human

Predicted Reactivity: Mouse,Rat,Dog,Rabbit

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human CXorf21

Isotype: IgG

Application Details

Application Notes: FCM(1:300-5000), IF(IHC-P)(1:50-200)

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, 0.02 % 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: -20 °C

Storage Comment: Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Expiry Date: 12 months

Target Details for CXorf21

Target: CXorf21 (TASL) (TLR Adaptor Interacting With Endolysosomal SLC15A4 (TASL))

Alternative Name: CXorf21

Background:

Synonyms: Chromosome X open reading frame 21, FLJ11577, Hypothetical protein LOC80231, Uncharacterized protein CXorf21, CX021_HUMAN.

Background: 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. There are a number of conditions related to an unsual number and combination of sex chromosomes being inherited. 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 which affect males more frequently as males carry a single X chromosome. The CXorf21 gene product has been provisionally designated CXorf21 pending further characterization.

Gene ID: 80231

UniProt: Q9HAI6