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

Rabbit Anti-FAM5B antibody
Rabbit Anti-FAM5B antibody
BMP/retinoic acid-inducible neural-specific protein 2; DBCCR1-like protein 2; Fam5b; BRNP2_HUMAN; Protein FAM5B.
Total
(Vip priceV)
Regular members: $334.4
  • Save more [Favourable] 30% discount
  • NO.:SL20081R
    Clonality:Polyclonal
    Immunogen Species:Rabbit
    React Species:(predicted: Human,)
    Applications:ELISA
    concentration:1mg/ml
  • Goods click count:15
  • Product Spec:
  • Quantity: - +
  • Limit points for buying:0 Points
  • Manual
  • Add to cart Inquiry Add to favorite
View History [Clear]

Details

Product Name FAM5B
Chinese Name FAM5B蛋白抗体
Alias BMP/retinoic acid-inducible neural-specific protein 2; DBCCR1-like protein 2; Fam5b; BRNP2_HUMAN; Protein FAM5B.  
Research Area Cell biology  immunology  
Immunogen Species Rabbit
Clonality Polyclonal
React Species (predicted: Human, )
Applications ELISA=1:5000-10000 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
Theoretical molecular weight 85kDa
Cellular localization cytoplasmic 
Form Liquid
Concentration 1mg/ml
immunogen KLH conjugated synthetic peptide derived from human FAM5B: 331-430/784 
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 BRINP2 is a 783 amino acid secreted protein that belongs to the FAM5 family. Existing as two alternatively spliced isoforms, BRINP2 is encoded by a gene that maps to human chromosome 1, which spans 260 million base pairs, contains over 3,000 genes and comprises nearly 8% of the human genome. Chromosome 1 houses a large number of disease-associated genes, including those that are involved in familial adenomatous polyposis, Stickler syndrome, Parkinson’s disease, Gaucher disease, schizophrenia and Usher syndrome. Aberrations in chromosome 1 are found in a variety of cancers, including head and neck cancer, malignant melanoma and multiple myeloma.

Subcellular Location:
Secreted.

Similarity:
Belongs to the FAM5 family.
Contains 1 MACPF domain.

SWISS:
Q9C0B6

Gene ID:
57795

Database links:

Entrez Gene: 57795 Human

Entrez Gene: 240843 Mouse

Entrez Gene: 286895 Rat

SwissProt: Q9C0B6 Human

SwissProt: Q6DFY8 Mouse

SwissProt: Q8K1M8 Rat

Unigene: 495918 Human

Unigene: 329579 Mouse

Unigene: 22596 Rat



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.