Rabbit Anti-MAGIX antibody | Sunlong Medical

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FLJ21687; JM10; MAGI family member, X-linked; MAGIX; MAGIX_HUMAN; MGC138889; PDZ domain containing protein; PDZ domain containing, X chromosome; PDZ domain-containing protein MAGIX; PDZX.

Cat:

SL18630R

Species Reactivity：

Human,

Immunogen：

KLH conjugated synthetic peptide derived from human MAGIX:201-300/334

Format：

Liquid

Storage instructions：

Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.

Concentration：

1mg/ml

Clonality：

Polyclonal

Isotype：

IgG

Applications：

WB=1:500-2000ELISA=1:5000-10000IHC-P=1:100-500IHC-F=1:100-500ICC=1:100-500IF=1:100-500（Paraffin sections need to do antigen repair）not yet tested in other applications.optimal dilutions/concentrations should be determined by the end user.

Host：

Rabbit

Product Overview：

Sample: HepG2(Human) Cell Lysate at 30 ugPrimary: Anti-MAGIX (SL18630R) at 1/300 dilutionSecondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilutionPredicted band size: 35 kDObserved band size: 35 kDParaformaldehyde-fixed, paraffin embedded (human liver tissue); Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15min; Block endogenous peroxidase by 3% hydrogen peroxide for 20 minutes; Blocking buffer (normal goat serum) at 37°C for 30min; Antibody incubation with (MAGIX) Polyclonal Antibody, Unconjugated (SL18630R) at 1:400 overnight at 4°C, followed by operating according to SP Kit(Rabbit) (sp-0023) instructionsand DAB staining.

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Unit:

Price: $228.00

Product PDFs

Datasheet: Down Datasheet

Other Information
Citations
Protein Attributes
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MAGIX is a 334 amino acid protein that contains one PDZ (DHR) domain and exists as three alternatively spliced isoforms. The gene encoding MAGIX maps to human chromosome Xp11.23. Chromosome X consists of about 153 million base pairs and nearly 1,000 genes. The combination of a 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 unusual number and combination of sex chromosomes being inherited, including Turner's syndrome, Klinefelter's syndrome and 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.

Similarity:
Contains 1 PDZ (DHR) domain.

SWISS:
Q9H6Y5

Gene ID:
79917

Database links:

Entrez Gene: 79917 Human

SwissProt: Q9H6Y5 Human

Unigene: 193170 Human

Picture

Paraformaldehyde-fixed, paraffin embedded (human liver tissue); Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15min; Block endogenous peroxidase by 3% hydrogen peroxide for 20 minutes; Blocking buffer (normal goat serum) at 37°C for 30min; Antibody incubation with (MAGIX) Polyclonal Antibody, Unconjugated (SL18630R) at 1:400 overnight at 4°C, followed by operating according to SP Kit(Rabbit) (sp-0023) instructionsand DAB staining.

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