Comparison

Human Serum Albumin [1.B.731]

Item no. 20-272-191604
Manufacturer GENWAY
Amount 0.5 mg
Category
Type Antibody
Applications ELISA
Clone 1. B. 731
Specific against Human (Homo sapiens)
ECLASS 10.1 32160702
ECLASS 11.0 32160702
UNSPSC 12352203
Alias GWB-7CF980
Similar products 20-272-191604
Available
Genway ID:
GWB-7CF980
Clone:
1. B. 731
Isotype:
IgG1
Immunogen:
Full length native protein (purified) (Human).
Antigen Species:
Human
Specificity:
No crossreactivity with other human proteins tested. Does not crossreact with BSA or egg white albumin.
Target:
Human Serum Albumin
Localization:
Secreted
Concentration:
4. 45 mg/ml Storage
Preservative:
0. 1% Sodium Azide. Constituents: 40% Glycerol PBS. pH 7. 4
Application Note:
ELISA: Use at an assay dependent dilution. Not tested in other applications. Optimal dilutions/concentrations should be determined by the end user. Cellular
Localization:
Secreted Myeloma: Sp2/0 Albumin is a soluble monomeric protein which comprises about one-half of the blood serum protein. Albumin functions primarily as a carrier protein for steroids fatty acids and thyroid hormones and plays a role in stabilizing extracellular fluid volume. Mutations in this gene on chromosome 4 result in various anomalous proteins. Albumin is a globular unglycosylated serum protein of molecular weight 65 000. The human albumin gene is 16 961 nucleotides long from the putative \' cap\' site to the first poly(A) addition site. It is split into 15 exons which are symmetrically placed within the 3 domains that are thought to have arisen by triplication of a single primordial domain. Albumin is synthesized in the liver as preproalbumin which has an N-terminal peptide that is removed before the nascent protein is released from the rough endoplasmic reticulum. The product proalbumin is in turn cleaved in the Golgi vesicles to produce the secreted albumin.
Function:
Serum albumin the main protein of plasma has a good binding capacity for water Ca(2+) Na(+) K(+) fatty acids hormones bilirubin and drugs. Its main function is the regulation of the colloidal osmotic pressure of blood.
Subcellular Location:
Secreted.
Tissue Specificity:
Plasma.
Ptm:
Kenitra variant is partially O-glycosylated at Thr-620. It has two new disulfide bonds Cys-600 to Cys-602 and Cys-601 to Cys-606.
Ptm:
Glycated in diabetic patients.
Polymorphism:
The sequence shown is that of variant albumin A.
Disease:
Defects in ALB are a cause of familial dysalbuminemic hyperthyroxinemia (FDH) [MIM:103600]. FDH is a form of euthyroid hyperthyroxinemia that is due to increased affinity of ALB for T(4). It is the most common cause of inherited euthyroid hyperthyroxinemia in Caucasian population.
Disease:
A variant structure of albumin could lead to increased binding of zinc resulting in an asymptomatic augmentation of zinc concentration in the blood [MIM:194470].
Miscellaneous:
Acetylated on Lys-223 by acetylsalicylic acid.
Similarity:
Belongs to the ALB/AFP/VDB family.
Similarity:
Contains 3 albumin domains.

Note: The presented information and documents (Manual, Product Datasheet, Safety Datasheet and Certificate of Analysis) correspond to our latest update and should serve for orientational purpose only. We do not guarantee the topicality. We would kindly ask you to make a request for specific requirements, if necessary.

All products are intended for research use only (RUO). Not for human, veterinary or therapeutic use.

Amount: 0.5 mg
Available: In stock
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