CXorf21 antibody (AA 165-215) (AbBy Fluor® 488)
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- Target See all CXorf21 products
- CXorf21 (Chromosome X Open Reading Frame 21 (CXorf21))
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Binding Specificity
- AA 165-215
- Reactivity
- Human, Mouse, Rat
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Host
- Rabbit
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Clonality
- Polyclonal
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Conjugate
- This CXorf21 antibody is conjugated to AbBy Fluor® 488
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Application
- Western Blotting (WB), Flow Cytometry (FACS), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- Cross-Reactivity
- Human, Mouse, Rat
- Purification
- Purified by Protein A.
- Immunogen
- KLH conjugated synthetic peptide derived from human CXorf21
- Isotype
- IgG
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- Application Notes
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FCM 1:20-100
IF(IHC-P) 1:50-200 - Restrictions
- For Research Use only
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- 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. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
- Expiry Date
- 12 months
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- Target
- CXorf21 (Chromosome X Open Reading Frame 21 (CXorf21))
- Alternative Name
- CXorf21 (CXorf21 Products)
- Synonyms
- CXorf21 antibody, chromosome X open reading frame 21 antibody, RIKEN cDNA 5430427O19 gene antibody, chromosome X open reading frame, human CXorf21 antibody, CXorf21 antibody, 5430427O19Rik antibody, CXHXorf21 antibody
- Background
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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
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