TEL: +86 571 56623320    EMAIL: [email protected]

Rabbit Anti-C9ORF43 antibody
Rabbit Anti-C9ORF43 antibody
Uncharacterized protein C9orf43; Chromosome 9 open reading frame 43; Hypothetical protein LOC257169; MGC17358; CI043_HUMAN.
Total
(Vip priceV)
Regular members: $334.4
View History [Clear]

Details

Product Name C9ORF43
Chinese Name 9号染色体开放阅读框43抗体
Alias Uncharacterized protein C9orf43; Chromosome 9 open reading frame 43; Hypothetical protein LOC257169; MGC17358; CI043_HUMAN.  
Research Area Cell biology  Developmental biology  Neurobiology  
Immunogen Species Rabbit
Clonality Polyclonal
React Species Mouse,  (predicted: Human, )
Applications WB=1:500-2000 ELISA=1:5000-10000 IHC-P=1:100-500 IHC-F=1:100-500 ICC=1:100-500 IF=1:100-500 (Paraffin sections need antigen repair)
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
Theoretical molecular weight 52kDa
Form Liquid
Concentration 1mg/ml
immunogen KLH conjugated synthetic peptide derived from human C9ORF43: 221-320/461 
Lsotype IgG
Purification affinity purified by Protein A
Buffer Solution 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
Storage Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.
Attention This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed PubMed
Product Detail Chromosome 9 consists of about 145 million bases and 4% of the human genome and encodes nearly 900 genes. Considered to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias. The C9orf43 gene product has been provisionally designated C9orf43 pending further characterization.

SWISS:
Q8TAL5

Gene ID:
257169

Database links:

Entrez Gene: 257169 Human

SwissProt: Q8TAL5 Human

Unigene: 632691 Human



Product Picture
Sample:
Placenta(Mouse) Lysate at 40 ug
Primary: Anti-C9ORF43 (SL9493R) at 1/300 dilution
Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution
Predicted band size: 52 kD
Observed band size: 52 kD
Sample:
B16 (Mouse) Cell Lysate at 40 ug
Primary: Anti-C9ORF43 (SL9493R) at 1/300 dilution
Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution
Predicted band size: 52 kD
Observed band size: 52 kD

References (0)

No References

Bought notes(bought amounts latest0)

No one bought this product
Total 0 records, divided into1 pages First Prev Next Last

User Comment(Total0User Comment Num)

  • No comment
Total 0 records, divided into1 pages First Prev Next Last
Username: Anonymous user
E-mail:
Rank:
Content:
Verification code: captcha

Call us

+86 571 56623320

Address

Room 1-315, Kongle Changqing Building, No. 160 Guangye Road,Gongshu District, Hangzhou City, Zhejiang Province, China

Join Us with

Leave a message
* To protect against spam, please pass the CAPTCHA test below.