product summary
request information :
company name :
MyBioSource
product type :
antibody
product name :
Goat anti Human Albumin
catalog :
MBS315799
quantity :
10 ml
price :
290 USD
clonality :
polyclonal
host :
goat
reactivity :
human
more info or order :
product information
catalog number :
MBS315799
products type :
Antibody
products full name :
Goat anti Human Albumin
products short name :
Albumin
products name syn :
Goat Antibody to Human Serum Albumin
other names :
albumin; Serum albumin; serum albumin; OTTHUMP00000160370; OTTHUMP00000196832; OTTHUMP00000220435; OTTHUMP00000220436; OTTHUMP00000220438; OTTHUMP00000220439; growth-inhibiting protein 20; cell growth inhibiting protein 42; albumin; N/A
other gene names :
ALB; ALB; PRO0883; PRO0903; PRO1341; DKFZp779N1935; N/A
uniprot entry name :
ALBU_HUMAN
clonality :
Polyclonal
host :
Goat
reactivity :
Human
sequence length :
609
specificity :
Albumin. Monospecific by immunoelectrophoresis when tested against pooled human plasma and twice concentrated pooled human serum.
purity :
Delipidation. Product is 0.2um filtered.
form :
Monospecific, Liquid
concentration :
Total protein: 9.1g/dL. Becker titer: 7.2mg/ml
storage stability :
Short-term (up to 7 days) store at 2 to 8 degree C. Long term, aliquot and store at -20 degree C. If aliquoted for long term storage, fill volume should be equal to or greater than 50% of the nominal fill volume of the vial used. Avoid repeated freeze/tha
other info1 :
Immunogen: Purified human Albumin
other info2 :
Buffer: Tris-saline, pH 7.4. Preservative: 0.1% Sodium azide. Important Note: Centrifuge before opening to ensure complete recovery of vial contents. Warnings: This product contains sodium azide, which has been classified as Xn (Harmful), in European Directive 67/548/EEC in the concentration range of 0.1-1.0%. When disposing of this reagent through lead or copper plumbing, flush with copious volumes of water to prevent azide build-up in drains.
products categories :
Polyclonal Antibodies to Proteins and Bioactive Peptides
ncbi gi num :
412163
ncbi acc num :
CAA00606.1
uniprot acc num :
P02768
ncbi mol weight :
69,367 Da
ncbi pathways :
Bile Acid And Bile Salt Metabolism Pathway 106144!!FOXA2 And FOXA3 Transcription Factor Networks Pathway 137911!!Formation Of Platelet Plug Pathway 106029!!HDL-mediated Lipid Transport Pathway 106158!!Hemostasis Pathway 106028!!Lipid Digestion, Mobilization, And Transport Pathway 106111!!Lipoprotein Metabolism Pathway 106156!!Metabolism Of Lipids And Lipoproteins Pathway 160976!!Platelet Activation Pathway 106034!!Platelet Degranulation Pathway 106050
ncbi summary :
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. Albumin is a globular unglycosylated serum protein of molecular weight 65,000. 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. [provided by RefSeq]
uniprot summary :
Function: Serum albumin, the main protein of plasma, has a good binding capacity for water, Ca2+, Na+, K+, fatty acids, hormones, bilirubin and drugs. Its main function is the regulation of the colloidal osmotic pressure of blood. Major zinc transporter in plasma, typically binds about 80% of all plasma zinc. Ref.33. Subcellular location: Secreted. Tissue specificity: Plasma. Ref.35. Post-translational modification: 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.Glycated in diabetic patients.Phosphorylation sites are present in the extracelllular medium.Acetylated on Lys-223 by acetylsalicylic acid. Polymorphism: A variant structure of albumin could lead to increased binding of zinc resulting in an asymptomatic augmentation of zinc concentration in the blood. The sequence shown is that of variant albumin A. Involvement in 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 T4. It is the most common cause of inherited euthyroid hyperthyroxinemia in Caucasian population. Ref.64 Ref.65 Ref.66 Ref.67. Sequence similarities: Belongs to the ALB/AFP/VDB family.Contains 3 albumin domains. Caution: A peptide arising from positions 166 to 174 was originally (Ref.23 and Ref.24) termed neurotensin-related peptide (NRP) or kinetensin and was thought to regulates fat digestion, lipid absorption, and blood flow. Sequence caution: The sequence AAF22034.1 differs from that shown. Reason: Erroneous initiation. Translation N-terminally extended.The sequence AAF69644.1 differs from that shown. Reason: Erroneous initiation. Translation N-terminally extended.The sequence AAG35503.1 differs from that shown. Reason: Erroneous initiation. Translation N-terminally extended.
size :
10 ml
price :
290 USD
more info or order :
company information
MyBioSource
P.O. Box 153308
San Diego, CA 92195-3308
sales@mybiosource.com
www.mybiosource.com
1-888-627-0165
headquarters: USA
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