Anti-Sheep Albumin, Antiserum, (Polyclonal) (rabbit serum) | MyBioSource MBS524089 product information

product summary

company name :

MyBioSource

product type :

antibody

product name :

Anti-Sheep Albumin, Antiserum, (Polyclonal) (rabbit serum)

catalog :

MBS524089

quantity :

2 mL

price :

290 USD

clonality :

polyclonal

host :

rabbit

conjugate :

nonconjugated

reactivity :

human

application :

immunoprecipitation

more info or order :

MyBioSource product webpage

image

image 1 :

product information

catalog number :

MBS524089

products type :

Antibody

products full name :

Anti-Sheep Albumin, Antiserum, (Polyclonal) (rabbit serum)

products short name :

[Albumin]

products name syn :

[Albumin, Antiserum, (Polyclonal) (rabbit serum); Rabbit Anti-Sheep Albumin]

other names :

[albumin; Serum albumin; serum albumin; albumin (32 AA); albumin (AA 34); growth-inhibiting protein 20; cell growth inhibiting protein 42; albumin]

other gene names :

[ALB; ALB; PRO0883; PRO0903; PRO1341]

uniprot entry name :

ALBU_HUMAN

clonality :

Polyclonal

isotype :

Rabbit Serum

host :

Rabbit

reactivity :

Sheep

sequence length :

609

specificity :

Albumin

form :

Antiserum

concentration :

Neat serum

storage stability :

Divide into useful aliquots and store at -20 degree C.

tested application :

Immunoprecipitation (IP), Immunodiffusion (ID)

app notes :

This antibody is suitable for use in immunoprecipitation and immunodiffusion.

image1 heading :

Testing Data

other info2 :

Presentation: 2 ml, liquid. Preservatives: 0.05% sodium azide

products description :

MBS524089 is an antiserum directed against sheep albumin and produced in rabbit. The antiserum of individual host animals was monitored for titre and specificity before pooling into uniform high titre lots.

ncbi gi num :

178344

ncbi acc num :

AAA98797.1

uniprot acc num :

P02768

ncbi mol weight :

69,367 Da

ncbi pathways :

Bile Acid And Bile Salt Metabolism Pathway (106144); Binding And Uptake Of Ligands By Scavenger Receptors Pathway (771599); FOXA2 And FOXA3 Transcription Factor Networks Pathway (137911); HDL-mediated Lipid Transport Pathway (106158); Hemostasis Pathway (106028); Lipid Digestion, Mobilization, And Transport Pathway (106111); Lipoprotein Metabolism Pathway (106156); Metabolism Pathway (477135); Metabolism Of Lipids And Lipoproteins Pathway (160976); Platelet Activation, Signaling And Aggregation Pathway (106034)

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, Jul 2008]

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.32. Subcellular location: Secreted. Tissue specificity: Plasma. 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 extracellular 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: Familial dysalbuminemic hyperthyroxinemia (FDH) [MIM:103600]: 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.Note: The disease is caused by mutations affecting the gene represented in this entry. Ref.61 Ref.62 Ref.63 Ref.64. 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 regulate 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.

size1 :

2 mL

price1 :

290 USD

more info or order :

MyBioSource product webpage