PIPA5116999

USH1C Polyclonal Antibody, Invitrogen™

Manufacturer: Thermo Scientific

Select a Size

Pack Size SKU Availability Price
Each of 1 PIPA5116999-Each-of-1 In Stock ₹ 46,502.50

PIPA5116999 - Each of 1

₹ 46,502.50

In Stock

Quantity

1

Base Price: ₹ 46,502.50

GST (18%): ₹ 8,370.45

Total Price: ₹ 54,872.95

Antigen

USH1C

Classification

Polyclonal

Conjugate

Unconjugated

Gene

USH1C

Gene Alias

2010016F01Rik; AIE75; AIE-75; Antigen NY-CO-38/NY-CO-37; autoimmune enteropathy-related antigen AIE-75; DFNB18; DFNB18A; harmonin; harmonin a1; harmonin pseudogene; hypothetical protein LOC530709; hypothetical protein LOC564412; NY-CO-37; NY-CO-38; PDZ domain-containing protein; PDZ-45; PDZ73; PDZ-73; PDZ-73 protein; PDZ-73/NY-CO-38; PDZD7C; Protein PDZ-73; Renal carcinoma antigen NY-REN-3; USH1 protein network component harmonin; Ush1c; ush1cpst; Usher syndrome 1C; Usher syndrome 1C (autosomal recessive, severe); Usher syndrome 1C homolog; usher syndrome type-1C protein; Usher syndrome type-1C protein homolog; zgc:136806

Host Species

Rabbit

Purification Method

Affinity chromatography

Regulatory Status

RUO

Gene ID (Entrez)

10083, 308596, 72088

Content And Storage

-20° C, Avoid Freeze/Thaw Cycles

Form

Liquid

Applications

Western Blot

Concentration

3.27 mg/mL

Formulation

PBS with 50% glycerol and 0.02% sodium azide; pH 7.3

Gene Accession No.

Q9ES64, Q9Y6N9

Gene Symbols

USH1C

Immunogen

Recombinant fusion protein containing a sequence corresponding to amino acids 1-100 of zebrafish USH1C (NP_0010350181)

Quantity

100 μL

Primary or Secondary

Primary

Target Species

Human, Mouse, Rat

Product Type

Antibody

Isotype

IgG

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Description

  • Positive Samples: HT-29, Mouse kidney, Mouse small intestine, Rat testis, Rat kidney Immunogen sequence: MERKVAREFR HKVELLIDNE AEKDYLYDVL RMYHQSMDLP VLVGDLKLVI NEPKRLPLFD AIRPLIPLKH QVQYDQLTPK RSRKLKEVRL DRTHPEGLGL This gene encodes a scaffold protein that functions in the assembly of Usher protein complexes
  • The protein contains PDZ domains, a coiled-coil region with a bipartite nuclear localization signal and a PEST degradation sequence
  • Defects in this gene are the cause of Usher syndrome type 1C and non-syndromic sensorineural deafness autosomal recessive type 18
  • Multiple transcript variants encoding different isoforms have been found for this gene.