CBLIF antibody
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935106861
info@markelab.com
name
CBLIF antibody
category
Primary Antibodies
provider
FineTest
reference
FNab10110
tested applications
ELISA, WB, IF
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.
Documents del producto
Product specifications
| Category | Primary Antibodies |
| Immunogen Target | GIF (CBLIF) |
| Host | Rabbit |
| Reactivity | Human, Mouse |
| Recommended Dilution | WB: 1:500 - 1:2000; IF: 1:50 - 1:200 |
| Clonality | polyclonal |
| Conjugation | Unconjugated |
| Isotype | IgG |
| Observed MW | 45kDa |
| Purity | ≥95% as determined by SDS-PAGE |
| Purification | Immunogen affinity purified |
| Size 1 | 100µg |
| Form | liquid |
| Tested Applications | ELISA, WB, IF |
| Storage | PBS with 0.02% sodium azide and 50% glycerol pH 7.3, -20℃ for 12 months(Avoid repeated freeze / thaw cycles.) |
| UniProt ID | P27352 |
| Gene ID | 2694 |
| Alias | Cobalamin binding intrinsic factor,Gastric intrinsic factor,Intrinsic factor (IF, INF),CBLIF,GIF,IFMH |
| Background | Antibody anti-CBLIF |
| Status | RUO |
| Note | Mol. Weight 45 kDa |
Descripción
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Human Anti-CBLIF (Cobalamin binding intrinsic factor) Antibody ELISA Kit
Ver Producto
CBLIF antibody
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.
Ver ProductoCBLIF antibody
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.
Ver Producto