• Immunofluorescent staining of FFPE human U-2 OS cells with CBLIF antibody (red) and DAPI nuclear stain (blue). HIER: steam section in pH6 citrate buffer for 20 min.
1 1

NSJ Bioreagents

RQ7732

CBLIF Antibody / Cobalamin binding intrinsic factor / GIF

CBLIF Antibody / Cobalamin binding intrinsic factor / GIF

$449.00 USD
$449.00 USD
Sale Sold out
Shipping calculated at checkout.
Size

This gene is a member of the cobalamin transport protein family. It encodes a glycoprotein secreted by parietal cells of the gastric mucosa and is required for adequate absorption of vitamin B12. Vitamin B12 is necessary for erythrocyte maturation and mutations in this gene may lead to congenital pernicious anemia.

Specifications

Family Primary antibody
Formulation 0.5mg/ml if reconstituted with 0.2ml sterile DI water
Format Antigen affinity purified
Host Animal Rabbit
Clonality Polyclonal (rabbit origin)
Isotype Rabbit IgG
Species Reactivity Human, Mouse
Application WB, IF, FACS, Direct ELISA
Application Details Western blot: 0.5-1ug/ml,Immunofluorescence: 5ug/ml,Flow cytometry: 1-3ug/million cells,Direct ELISA: 0.1-0.5ug/ml
Application Note Optimal dilution of the CBLIF antibody should be determined by the researcher.
Immunogen E. coli-derived recombinant human protein (amino acids E128-Y417) was used as the immunogen for the CBLIF antibody.
Buffer Lyophilized from 1X PBS with 2% Trehalose
Purity Antigen affinity purified
Storage After reconstitution, the CBLIF antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
Limitation This CBLIF antibody is available for research use only.
Uniprot # P27352
Status Available
PDF Link https://www.nsjbio.com/tds-pdf/cblif-antibody-cobalamin-binding-intrinsic-factor-gif-rq7732
Title CBLIF Antibody / Cobalamin binding intrinsic factor / GIF
Description This gene is a member of the cobalamin transport protein family. It encodes a glycoprotein secreted by parietal cells of the gastric mucosa and is required for adequate absorption of vitamin B12. Vitamin B12 is necessary for erythrocyte maturation and mutations in this gene may lead to congenital pernicious anemia.
View full details