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binds vitamin B12 (cobalamin) [RGD, Feb 2006].. Additionally we are shipping Intrinsic Factor Kits (39) and Intrinsic Factor Proteins (18) and many more products for this protein.
Showing 10 out of 70 products:
Human Polyclonal Intrinsic Factor Primary Antibody for WB - ABIN516030
Maloum, Allaire, Gagné-Sansfaçon, Roy, Belleville, Sarret, Morisset, Carrier, Mishina, Kaestner, Perreault: Epithelial BMP signaling is required for proper specification of epithelial cell lineages and gastric endocrine cells. in American journal of physiology. Gastrointestinal and liver physiology 2011
The gastric intrinsic factor (GIF) 290C heterozygous/fucosyltransferase 2 (secretor status included (show FUT2 Antibodies)) protein (FUT2 (show FUT2 Antibodies)) rs601338 secretor variant combined genotype was indicated in 6 of the 37 neural tube defects (NTDs) fetuses.
the present findings reveal that High-altitude polycythemia -induced gastric mucosal lesion inspires the protection responses by up-regulating APOA4 (show APOA4 Antibodies) and APOC3 (show APOC3 Antibodies), and down-regulating GIF.
study reports that FUT2 (show FUT2 Antibodies) secretor variant influences GIF secretion in B12 (show NDUFB3 Antibodies) deficient cases bearing GIF heterozygous mutations, in absence of H. pylori related gastritis
Our genetic screening of 154 families of patients with inherited cobalamin malabsorption revealed population-specific mutations, mutational hotspots, and functionally distinct regions in the three causal genes: CUBN (show CUBN Antibodies), AMN (show ABCD1 Antibodies), and GIF.
Acute lymphoblastic leukemia and vitamin B12 (show NDUFB3 Antibodies) deficiency secondary to a gastric intrinsic factor gene mutation
crystal structure of the complex between IF-Cbl and the cubilin IF-Cbl-binding-region (CUB(5-8)) determined at 3.3 A resolution
A polymorphism in the gastric intrinsic factor gene is associated with congenital intrinsic factor deficiency.
The parameters obtained for ligand and receptor binding in this study indicate that both full-length 50-kDA intrinsic factor and its 30-kDa and 20-kDa fragments may be involved in assimilation of cobalamin.
The Q5R mutation of the intrinsic factor gene predisposes to adult-onset pernicious anemia & other causes of low vitamin B12 (show NDUFB3 Antibodies). In this mutation, intrinsic factor secretion is preserved but B12 (show NDUFB3 Antibodies) absorption may be impaired.
a specific GIF mutation to be responsible for all Juvenile cobalamin deficiency cases of West-African origin so far was identified
Spasmolytic polypeptide (show TFF2 Antibodies)/trefoil (show TFF3 Antibodies) factor family 2 (TFF2 (show TFF2 Antibodies))-expressing metaplasia (SPEM)was immunoreactive for TFF2 (show TFF2 Antibodies), Mist1 and intrinsic factor, suggesting that SPEM derived from transdifferentiation of chief cells.
binds vitamin B12 (cobalamin)
gastric intrinsic factor (vitamin B synthesis)
, gastric intrinsic factor
, intrinsic factor
, pancreatic intrinsic factor
, gastric intrinsic factor-like