Anti-APOL1 Antibody

$99.00$319.00

Reactivity: Human
Applications: ELISA,WB,IHC
Conjugation: Various
Supplier: CUSABIO BIOTECH CO.

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Rabbit Anti-APOL1 Antibody (CSB-PA001940ESR2HU)

Supplier: CUSABIO BIOTECH CO.

Alternative names:

CSB-PA001940ESR2HU Antibody,Apo-L Antibody,ApoL Antibody,Apolipoprotein L-I Antibody,ApoL-I Antibody,APOL1 Antibody,APOL Antibody

More alternative names for the antibody
APO L antibody|Apo-L antibody|ApoL antibody|APOL I antibody|ApoL-I antibody|APOL1 antibody|APOL1_HUMAN antibody|APOLI antibody|Apolipoprotein L antibody|Apolipoprotein L I antibody|Apolipoprotein L-I antibody|Apolipoprotein L1 antibody|FSGS4 antibody
Anti-Apolipoprotein L 1 antibody [EPR2907(2)] (ab108315)
Close sc-390440|sc-30090|sc-18759|

Recommended applications: ELISA, WB, IHC

Recommended dilution: Recommended dilution:WB:1:500-2000,IHC:1:20-1:200

Recommended protocols: check protocols

Name

Anti-APOL1 Antibody

Catalogue No.

CSB-PA001940ESR2HU

Reactivity

Human

Immunogen

Recombinant human Apolipoprotein L1 protein (179-398AA)

Host

Rabbit

Applications

ELISA, WB, IHC

Recommended dilution

Recommended dilution:WB:1:500-2000,IHC:1:20-1:200

Clonality

Polyclonal

Conjugation

unconjugated

Isotype

IgG

Molecular weight

43 kDa

Purification

Antigen Affinity Purified

Storage

Shipped at 4 Celcius Degree. Upon delivery aliquot and store at -20 Celcius Degree or -80 Celcius Degree. Avoid repeated freeze.

Database links

Entrez Gene:8542( Human), Omim:603743( Human), SwissProt:O14791( Human), Unigene:114309( Human)

Protein function

May play a role in lipid exchange and transport throughout the body. May participate in reverse cholesterol transport from peripheral cells to the liver.

Protein tissue specificity

Plasma. Found on APOA-I-containing high density lipoprotein (HDL3). Expressed in pancreas, lung, prostate, liver, placenta and spleen.

Involvement in disease

Focal segmental glomerulosclerosis 4 (FSGS4) [MIM:612551]: A renal pathology defined by the presence of segmental sclerosis in glomeruli and resulting in proteinuria, reduced glomerular filtration rate and progressive decline in renal function. Renal insufficiency often progresses to end-stage renal disease, a highly morbid state requiring either dialysis therapy or kidney transplantation. . Note=The disease is caused by mutations affecting the gene represented in this entry.

Protein sequence and domain

Belongs to the apolipoprotein L family.

Protein post-translational modifications

Phosphorylated by FAM20C in the extracellular medium. .

Protein cellular localization

Secreted.

Research area

All research areas>Transport and Trafficking>Apolipoprotein
(View all antibody categories related to Transport and Trafficking)

Note

AntibodyPlus provides antibody trial sample for your own antibody validation and collects antibody reviews.

Supplier

CUSABIO BIOTECH CO.

Product type

Primary antibody

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