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  • KD/KO Validated

LIPH Polyclonal antibody

LIPH Polyclonal Antibody for IF, IHC, IP, WB, ELISA

Host / Isotype

Rabbit / IgG

Reactivity

human, mouse, rat

Applications

WB, IP, IHC, IF, ELISA

Conjugate

Unconjugated

Cat no : 16602-1-AP

Synonyms

AH, Lipase member H, lipase, member H, LIPH, LPD lipase related protein, LPDLR, mPA PLA1, mPA PLA1 alpha, MPAPLA1, Phospholipase A1 member B, PLA1B



Tested Applications

Positive WB detected inA549 cells, COLO 320 cells, mouse lung tissue
Positive IP detected inmouse lung tissue
Positive IHC detected inhuman pancreas tissue
Note: suggested antigen retrieval with TE buffer pH 9.0; (*) Alternatively, antigen retrieval may be performed with citrate buffer pH 6.0
Positive IF detected inA549 cells

Recommended dilution

ApplicationDilution
Western Blot (WB)WB : 1:500-1:1000
Immunoprecipitation (IP)IP : 0.5-4.0 ug for 1.0-3.0 mg of total protein lysate
Immunohistochemistry (IHC)IHC : 1:20-1:200
Immunofluorescence (IF)IF : 1:10-1:100
It is recommended that this reagent should be titrated in each testing system to obtain optimal results.
Sample-dependent, Check data in validation data gallery.

Product Information

16602-1-AP targets LIPH in WB, IP, IHC, IF, ELISA applications and shows reactivity with human, mouse, rat samples.

Tested Reactivity human, mouse, rat
Cited Reactivityhuman
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen LIPH fusion protein Ag9775
Full Name lipase, member H
Calculated Molecular Weight 51 kDa
Observed Molecular Weight 50-55 kDa
GenBank Accession NumberBC064941
Gene Symbol LIPH
Gene ID (NCBI) 200879
RRIDAB_2135352
Conjugate Unconjugated
Form Liquid
Purification MethodAntigen affinity purification
Storage Buffer PBS with 0.02% sodium azide and 50% glycerol pH 7.3.
Storage ConditionsStore at -20°C. Stable for one year after shipment. Aliquoting is unnecessary for -20oC storage. 20ul sizes contain 0.1% BSA.

Background Information

LIPH(Lipase member H) is also named as LPDLR, MPAPLA1, PLA1B. It is a phosphatidic acid-selective phospholipase A1 (PLA1) that produces 2-acyl lysophosphatidic acid (LPA) and belongs to the AB hydrolase superfamily and Lipase family.LIPH has a 12-residue lid region, which likely covers a catalytic pocket, and 4 potential N-linked glycosylation sites. Defects in LIPH are the cause of hypotrichosis type 7 (HYPT7).

Protocols

Product Specific Protocols
WB protocol for LIPH antibody 16602-1-APDownload protocol
IHC protocol for LIPH antibody 16602-1-APDownload protocol
IF protocol for LIPH antibody 16602-1-APDownload protocol
IP protocol for LIPH antibody 16602-1-APDownload protocol
Standard Protocols
Click here to view our Standard Protocols

Publications

SpeciesApplicationTitle
humanWB

Genet Med

Loss-of-function variants in C3ORF52 result in localized autosomal recessive hypotrichosis.

Authors - Liron Malki
humanIHC

Cell Oncol (Dordr)

Genomic analysis and filtration of novel prognostic biomarkers based on metabolic and immune subtypes in pancreatic cancer

Authors - Guangyu Chen
humanWB

J Cell Mol Med

LIPH promotes metastasis by enriching stem-like cells in triple-negative breast cancer.

Authors - Yixiao Zhang
  • KD Validated
humanIHC

Tumour Biol

Lipase member H is a novel secreted protein associated with a poor prognosis for breast cancer patients.

Authors - Meizi Cui
humanELISA,WB,IHC

Biochem Biophys Res Commun

Lipase member H is a novel secreted protein selectively upregulated in human lung adenocarcinomas and bronchioloalveolar carcinomas.

Authors - Yasuhiro Seki
humanIHC

Tumour Biol

Lipase member H frequently overexpressed in human esophageal adenocarcinomas.

Authors - Hisako Ishimine