Mannose-Binding Protein C (MBL2) Antibody

195€ (20 µl)
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935106861
info@markelab.com
name
Mannose-Binding Protein C (MBL2) Antibody
category
Primary Antibodies
provider
Abbexa
reference
abx004465
tested applications
ELISA, WB, IHC
Description
MBL2 Antibody is a Rabbit Polyclonal antibody against MBL2. This gene encodes the soluble mannose-binding lectin or mannose-binding protein found in serum. The protein encoded belongs to the collectin family and is an important element in the innate immune system. The protein recognizes mannose and N-acetylglucosamine on many microorganisms, and is capable of activating the classical complement pathway. Deficiencies of this gene have been associated with susceptibility to autoimmune and infectious diseases.
Documents del producto
Instrucciones
Data sheet
Product specifications
Category | Primary Antibodies |
Immunogen Target | Mannose-Binding Protein C (MBL2) |
Host | Rabbit |
Reactivity | Human, Mouse |
Recommended Dilution | ELISA: 1 µg/ml, WB: 1/100 - 1/500, IHC-P: 1/50 - 1/200. Not tested in IHC-F. Optimal dilutions/concentrations should be determined by the end user. |
Clonality | Polyclonal |
Conjugation | Unconjugated |
Isotype | IgG |
Purification | Purified by affinity chromatography. |
Size 1 | 20 µl |
Size 2 | 100 µl |
Size 3 | 2 × 100 µl |
Form | Liquid |
Tested Applications | ELISA, WB, IHC |
Buffer | PBS, pH 7.3, containing 0.02% sodium azide, 50% glycerol. |
Availability | Shipped within 5-10 working days. |
Storage | Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles. |
Dry Ice | No |
UniProt ID | P11226 |
Gene ID | 4153 |
NCBI Accession | NP_000233.1 |
OMIM | 154545 |
Background | Antibody anti-MBL2 |
Status | RUO |
Note | Concentration: > 0.2 mg/ml - |
Descripción
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MBL2 antibody
This gene encodes the soluble mannose-binding lectin or mannose-binding protein found in serum. The protein encoded belongs to the collectin family and is an important element in the innate immune system. The protein recognizes mannose and N-acetylglucosamine on many microorganisms, and is capable of activating the classical complement pathway. Deficiencies of this gene have been associated with susceptibility to autoimmune and infectious diseases.
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